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Littérature scientifique sur le sujet « Acetamide »

Auteur : Grafiati

Publié le 4 juin 2021

Mis à jour le 6 septembre 2023

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Articles de revues sur le sujet "Acetamide"

Nagarsha, K. M., T. M. Sharanakumar, D. Ramesh, N. Y. Praveen Kumar, M. N. Kumarswamy, D. R. Ramesh et K. P. Latha. « NOVEL SYNTHESIS, CHARACTERIZATION AND ANTIMICROBIAL ACTIVITY OF N-(5BROMO-2-(5-PHENYL1,3,4-OXADIAZOL-2-YL)NAPHTHA[2,1-B]FURAN-1- YL)ACETAMIDE AND N-(5-NITRO-2-(5-PHENYL-1,3,4- OXADIAZOL-2-YL)NAPHTHA[2,1-BFURAN-1-YL]ACETAMIDE AND THEIR DERIVATIVES ». RASAYAN Journal of Chemistry 16, n^o 01 (2023) : 167–75. http://dx.doi.org/10.31788/rjc.2023.1618088.

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The novel derivatives of naphtho-furan such N-(5bromo-2-(5-phenyl-1,3,4-oxadiazol-2-yl)naphtha[2,1-b]furan-1- yl)acetamide (8), N-(5-bromo-2-(hydrazinecarbonyl)naphtha[2,1-b]furan-1-yl]acetamide (7), ethyl-1-acetamido-5- bromonaphtho[2,1-b]furan-2-carboxylate (6), N-(5-nitro-2-(5-phenyl-1,3,4-oxadiazol-2-yl)naphtha[2,1-bfuran-1- yl]acetamide (5),N-(2-(hydrazinecarbonyl)-5-nitronaphtho[2,1-b]furan-1-yl)acetamide (4), ethyl-1-acetamido-5- nitrpnaphtho[2,1-b]furan-2-carboxylate (3), are prepared by ethyl-1-acetamidonaphtho[2,1-b]furan-2-carboxyate and ethyl 1-aminonaphtho[2,1-b]furan-2-carboxylate. All newly synthesized compounds were confirmed by Mass, NMR, and FTIR spectroscopic techniques. Those compounds were used for antimicrobial activity it exhibits good antibacterial and anti-functional activity.

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Qiu, Guanyinsheng, Yuewen Li, Lele Ma et Hongwei Zhou. « KBr/K2S2O8-mediated dibromohydration of N-(2-alkynylaryl)acetamide ». Organic Chemistry Frontiers 4, n^o 6 (2017) : 1069–73. http://dx.doi.org/10.1039/c6qo00840b.

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Girel, Sergey, Vadim Schütz, Laurent Bigler, Peter Dörmann et Margot Schulz. « Bioactive Nitrosylated and Nitrated N-(2-hydroxyphenyl)acetamides and Derived Oligomers : An Alternative Pathway to 2-Amidophenol-Derived Phytotoxic Metabolites ». Molecules 27, n^o 15 (26 juillet 2022) : 4786. http://dx.doi.org/10.3390/molecules27154786.

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Incubation of Aminobacter aminovorans, Paenibacillus polymyxa, and Arthrobacter MPI764 with the microbial 2-benzoxazolinone (BOA)-degradation-product 2-acetamido-phenol, produced from 2-aminophenol, led to the recently identified N-(2-hydroxy-5-nitrophenyl) acetamide, to the hitherto unknown N-(2-hydroxy-5-nitrosophenyl)acetamide, and to N-(2-hydroxy-3-nitrophenyl)acetamide. As an alternative to the formation of phenoxazinone derived from aminophenol, dimers- and trimers-transformation products have been found. Identification of the compounds was carried out by LC/HRMS and MS/MS and, for the new structure N-(2-hydroxy-5-nitrosophenyl)acetamide, additionally by 1D- and 2D-NMR. Incubation of microorganisms, such as the soil bacteria Pseudomonas laurentiana, Arthrobacter MPI763, the yeast Papiliotrema baii and Pantoea ananatis, and the plants Brassica oleracea var. gongylodes L. (kohlrabi) and Arabidopsis thaliana Col-0, with N-(2-hydroxy-5-nitrophenyl) acetamide, led to its glucoside derivative as a prominent detoxification product; in the case of Pantoea ananatis, this was together with the corresponding glucoside succinic acid ester. In contrast, Actinomucor elegans consortium synthesized 2-acetamido-4-nitrophenyl sulfate. 1 mM bioactive N-(2-hydroxy-5-nitrophenyl) acetamide elicits alterations in the Arabidopsis thaliana expression profile of several genes. The most responsive upregulated gene was pathogen-inducible terpene synthase TPS04. The bioactivity of the compound is rapidly annihilated by glucosylation.

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Gowda, Basavalinganadoddy Thimme, Jozef Kožíšek, Ingrid Svoboda et Hartmut Fuess. « Effect of Meta-Substitution on Solid State Geometry of N-(Aryl)-2,2,2-trichloro-acetamides, 3-XC6H4NH-CO-CCl3 and 3,5-X2C6H3NH-CO-CCl3 (X = Cl, CH3) ». Zeitschrift für Naturforschung A 62, n^o 1-2 (1 février 2007) : 91–100. http://dx.doi.org/10.1515/zna-2007-1-213.

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The crystal structures of N-(meta-substituted phenyl)-2,2,2-trichloro-acetamides such as N- (3-methylphenyl)-2,2,2-trichloro-acetamide, 3-CH3C6H4NH-CO-CCl3 (3MPTCA); N-(3-chlorophenyl)- 2,2,2-trichloro-acetamide, 3-ClC6H4NH-CO-CCl3 (3CPTCA); N-(3,5-dimethylphenyl)- 2,2,2-trichloro-acetamide, 3,5-(CH3)2C6H3NH-CO-CCl3 (35DMPTCA) and N-(3,5-dichlorophenyl)- 2,2,2-trichloro-acetamide, 3,5-Cl2C6H3NH-CO-CCl3 (35DCPTCA) have been determined at room temperature. The crystal system, space group, formula units and lattice constants (Å ) of the new structures are: 3MPTCA: orthorhombic, Pbca, Z = 8, a = 12.3199(11), b = 8.9719(8), c = 20.2058(15); 3CPTCA: orthorhombic, Fdd2, Z =16, a=19.285(4), b=40.765(8), c=5.5920(11); 35DMPTCA: triclinic, P1̄, Z = 2, a = 8.994(4), b = 9.9890(10), c = 14.760(5), α = 79.56(2)°, β = 73.32(3)°, γ = 86.47(2)°; and 35DCPTCA: orthorhombic, Pbca, Z = 8, a = 22.485(5), b=10.738(2), c=10.028(3). The compound 35DMPTCA has two molecules in its asymmetric unit, similar to o-NO2-, m-NO2- and p-CH3-substituted phenyl-trichloro-acetamides, while 3MPTCA, 3CPTCA and 35DCPTCA have one molecule each in their asymmetric units. The analysis of data indicates that the substitution of a strong electron withdrawing group such as a nitro group into PTCA at ortho or meta positions has a significant effect on the crystal parameters.

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Alagarsamy, Veerachamy, Viswas Raja Solomon, Mohaideen Thasthagir Sulthana, Meduri Satyasai Vijay et Bandi Narendhar. « Design and synthesis of quinazolinyl acetamides for their analgesic and anti-inflammatory activities ». Zeitschrift für Naturforschung B 70, n^o 8 (1 août 2015) : 597–604. http://dx.doi.org/10.1515/znb-2015-0035.

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AbstractA variety of novel 2-(substituted)-N-(4-oxo-2-phenylquinazolin-3(3H)-yl)acetamides were synthesized by the reaction of 2-chloro-N-(4-oxo-2-phenylquinazolin-3(3H)-yl)acetamide with various amines. The starting material, 2-chloro-N-(4-oxo-2-phenylquinazolin-3(3H)-yl)acetamide, was synthesized from anthranilic acid by the multistep process. The title compounds were investigated for analgesic, anti-inflammatory, and ulcerogenic index activities. Among those, the compound 2-(ethylamino)-N-(4-oxo-2-phenylquinazolin-3(3H)-yl)acetamide (V9) showed most potent analgesic and anti-inflammatory activities of the series and it is moderately more potent compared to the reference standard diclofenac sodium. Interestingly, the test compounds showed only mild ulcerogenic potential compared to aspirin.

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Chen, Xuanhua, Rongwei Guo et Zhongyuan Zhou. « N-[3-Acetamido-1,3-bis(4-ethylphenyl)butenyl]acetamide ». Acta Crystallographica Section E Structure Reports Online 58, n^o 6 (24 mai 2002) : o671—o672. http://dx.doi.org/10.1107/s1600536802008607.

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Eagle, Cassandra T., Nkongho Atem-Tambe, Kenneth K. Kpogo, Jennie Tan et Fredricka Quarshie. « (3-Methylbenzonitrile-κN)tetrakis(μ-N-phenylacetamidato)-κ4N:O;κ4O:N-dirhodium(II)(Rh—Rh) ». Acta Crystallographica Section E Structure Reports Online 69, n^o 12 (6 novembre 2013) : m639. http://dx.doi.org/10.1107/s1600536813029838.

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In the title compound, [Rh2(C8H8NO)4(C8H7N)], the four acetamidate ligands bridging the dirhodium core are arranged in a 2,2-transmanner. One RhIIatom is five-coordinate, in a distorted pyramidal geometry, while the other is six-coordinate, with a disorted octahedral geometry. For the six-coordinate RhIIatom, the axial nitrile ligand shows a non-linear Rh–nitrile coordination with an Rh—N—C bond angle of 166.4 (4)° and a nitrile N—C bond length of 1.138 (6) Å. Each unique RhIIatom is coordinated by atranspair of N atoms and atranspair of O atoms from the four acetamide ligands. The Neq—Rh—Rh—Oeqtorsion angles on the acetamide bridge varies between 12.55 (11) and 14.04 (8)°. In the crystal, the 3-methylbenzonitrile ring shows a π–π interaction with an inversion-related equivalent [interplanar spacing = 3.360 (6) Å]. A phenyl ring on one of the acetamide ligands also has a face-to-face π–π interaction with an inversion-related equivalent [interplanar spacing = 3.416 (5) Å].

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Que, Chuqiang, Peipei Huang, Zhanhui Yang, Ning Chen et Jiaxi Xu. « Intramolecular Carbene C-H Insertion Reactions of 2-Diazo-2-sulfamoylacetamides ». Molecules 24, n^o 14 (19 juillet 2019) : 2628. http://dx.doi.org/10.3390/molecules24142628.

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The intramolecular C-H insertions of carbenes derived from 2-diazo-2-sulfamoylacetamides were studied. 2-Diazo-2-sulfamoylacetamides were first prepared from chloroacetyl chloride and secondary amines through acylation followed by sequential treatments with sodium sulfite, phosphorus oxychloride, secondary amines, and 4-nitrobenzenesulfonyl azide. The results indicate that: (1) 2-diazo-N,N-dimethyl-2-(N,N-diphenylsulfamoyl)acetamide can take the formal aromatic 1,5-C-H insertion in its N-phenylsulfonamide moiety to afford the corresponding 1,3-dihydrobenzo[c]isothiazole-3-carboxamide 2,2-dioxide derivative; (2) no aliphatic C-H insertions occur for 2-diazo-2-(N,N-dialkylsulfamoyl)acetamides; and (3) for 2-diazo-N-phenyl-2-(N-phenylsulfamoyl)acetamides, the formal aromatic 1,5-C-H insertion in the N-phenylacetamide moiety is favorable to afford the corresponding 3-sulfamoylindolin-2-one derivatives as sole or major products. The intramolecular competitive aromatic 1,5-C-H insertion reactions of 2-diazo-2-sulfamoylacetamides with aryl groups on both amide and sulfonamide groups reveal that the N-aryl substituents on acetamide are more active than those on sulfonamide. The chemoselectivity is controlled by electronic effect of the aryl group.

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Gowda, Basavalinganadoddy Thimme, Helmut Paulus et Jozef Kožíšek. « Effect of Substitution on the Molecular Geometry of N-(2/3/4-Substituted-phenyl)-2,2-dichloro-acetamides, 2/3/4-XC6H4NH-CO-CHCl2 (X = CH3 or Cl) ». Zeitschrift für Naturforschung A 61, n^o 12 (1 décembre 2006) : 675–82. http://dx.doi.org/10.1515/zna-2006-1210.

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2MPDCAThe effect of ring substitution on the molecular geometry of amides of the type 2/3/4-XC6H4NHCO- CHCl2 (X = CH3 or Cl) has been studied by determining the crystal structures of the compounds N-(2-methylphenyl)-2,2-dichloro-acetamide, 2-CH3C6H4NH-CO-CHCl2 (); N-(3-methylphenyl)- 2,2-dichloro-acetamide, 3-CH3C6H4NH-CO-CHCl2 (3MPDCA) and N-(3-chlorophenyl)- 2,2-dichloro-acetamide, 3-ClC6H4NH-CO-CHCl2 (3CPDCA). The results are analyzed along with our earlier crystal structures of the amides N-(phenyl)-2,2-dichloro-acetamide, C6H5NH-COCHCl2 (PDCA); N-chloro-N-(phenyl)-2,2-dichloro-acetamide, C6H5NCl-CO-CHCl2 (NCPDCA); N-(4-methylphenyl)-2,2-dichloro-acetamide, 4-CH3C6H4NH-CO-CHCl2 (4MPDCA); N-(2-chlorophenyl)- 2,2-dichloro-acetamide, 2-ClC6H4NH-CO-CHCl2 (2CPDCA); N-(4-chlorophenyl)-2,2-dichloro- acetamide, 4-ClC6H4NH-CO-CHCl2 (4CPDCA). The results have also been compared and correlated with the crystal structure data of trichloro-acetamide analogues of the type 2/3/4- XC6H4NH-CO-CCl3 (X = CH3 or Cl): N-(phenyl)-2,2,2-trichloro-acetamide, N-(2-methylphenyl)- 2,2,2-trichloro-acetamide, N-(3-methylphenyl)-2,2,2-trichloro-acetamide, N-(4-methylphenyl)- 2,2,2-trichloro-acetamide, N-(2-chlorophenyl)-2,2,2-trichloro-acetamide, N-(3-chlorophenyl)-2,2,2- trichloro-acetamide, N-(4-chlorophenyl)-2,2,2-trichloro-acetamide, N-chloro-N-(phenyl)-2,2,2-trichloro- acetamide and N-(phenyl)-acetamide. The crystal system, space group, formula units and lattice constants in Å of the new structures are: 2MPDCA: monoclinic, P21/n, Z = 4, a = 4.7059(5), b = 11.600(1), c = 18.918(2), β = 94.702(9)° ; 3MPDCA: orthorhombic, P212121, Z = 4, a = 4.759(1), b = 10.543(3), c = 20.205(5); 3CPDCA: orthorhombic, Pnma, Z = 4, a = 9.935(1), b = 6.997(1), c = 14.140(2). 2MPDCA, 3MPDCA and 3CPDCA show a molecule each in their asymmetric units, in agreement with the observed 35Cl NQR spectra of the compounds

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Nagarsha, K. M., T. M. Sharanakumar, D. Ramesh, M. N. Kumarswamy et K. P. Latha. « SYNTHESIS, CHARACTERIZATION, AND ANTIBACTERIAL ACTIVITIES OF NAPHTHO[2,1-b]FURAN DERIVATIVES ». RASAYAN Journal of Chemistry 15, n^o 04 (2022) : 2477–84. http://dx.doi.org/10.31788/rjc.2022.1548052.

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The naphthofuran and its derivatives are important biological compounds so we have focused on the synthesis of naphthofuran derivatives. The synthesized compounds of ethyl 1-(acetylamino)-5-nitronaphtho[2,1-b]furan-2- carboxylate (3), and N-[2-(hydrazinylcarbonyl)-5-nitronaphtho[2,1-b]furan-1-yl]acetamide (4) used for the synthesis of N-(2-{[(2Z)-2-benzylidenehydrazinyl]carbonyl}-5-nitronaphtho[2,1-b]furan-1-yl)acetamide compounds of four derivatives 5 (a-d) and 1-acetamido-5-nitro-N-(5-oxo-2-phenylthiazolidin-3-yl)naphtha[2,1-b]furan-2-carboxamide compounds of four derivatives 6 (a-d). The prepared compounds were confirmed by FTIR NMR, and mass methods. The prepared naphthofuran derivatives used for the antibacterial activity versus both Gram(+ve) and Gram(-ve) bacteria show excellent results. Therefore the synthesized compounds are used for further antibacterial studies in the medical field.

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Thèses sur le sujet "Acetamide"

Gallagher, Julie Marie. « The synthesis of 1-acetamido-2,6-anhydro-1,7-deoxy-L-glycero-L-galactitol (N-[β-L-fucopyranosylomethyl]-acetamide) and related derivatives ». Scholarly Commons, 1989. https://scholarlycommons.pacific.edu/uop_etds/2182.

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One important goal of this thesis is the hydrogenation of the glycosyl cyanide, which has never been mentioned by any of the groups who have done work in this area, except for B. Coxon and G. Fletcher, who in 1964, reduced a tetra-O-acetyl-β-D-galactopyranosyl cyanide with lithium aluminum hydride. We were hoping to obtain, by reduction with hydrogen on Pd/C, an aminomethyl C-glycoside. It is believed that these aminomethyl C-glycosides are of potential biological importance especially in the area of AIDS and HIV therapy.

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Issac, Ibrahim Youhanna. « Studies in the lower temperature molten salts eutectics ». Thesis, University of Southampton, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.252705.

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Marchand, Pascal. « Synthese et evaluation pharmacologique de derives indoliques a activites immunosuppressive et antitumorale (doctorat chimie therapeutique) ». Nantes, 1999. http://www.theses.fr/1999NANT22VS.

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Zhang, Zichen. « Anticancer effects of hexamethylene bisacetamide on human colon carcinoma cells in vitro / ». Hong Kong : University of Hong Kong, 1999. http://sunzi.lib.hku.hk/hkuto/record.jsp?B21021065.

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Lundell, Sandra J. « Quantum Mechanical Studies of N-H···N Hydrogen Bonding in Acetamide Derivatives and Amino Acids ». DigitalCommons@USU, 2018. https://digitalcommons.usu.edu/etd/7309.

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Proteins are made of vast chains of amino acids that twist and fold into intricate designs. These structures are held in place by networks of noncovalent interactions. One of these, the hydrogen bond, forms bridges between adjacent pieces of the protein chain and is one of the most important contributors to the shape and stability of proteins. Hydrogen bonds come in all shapes and sizes and a full understanding of these not only aids in our understanding of proteins in general but can bridge the gap to finding cures to many protein-related diseases, such as sickle-cell anemia. The primary aim of this thesis is to discover if a specific type of hydrogen bond, the N-H···N bond, occurs within proteins and if so, if it contributes to the structure and stability of proteins.

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Borko, Matijević. « Građenje halogenidnih kompleksa kobalta(II) u rastopima smeše neorganskih soli i polarnih organskih jedinjenja ». Phd thesis, Univerzitet u Novom Sadu, Prirodno-matematički fakultet u Novom Sadu, 2011. https://www.cris.uns.ac.rs/record.jsf?recordId=77320&source=NDLTD&language=en.

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U ovoj doktorskoj disertaciji proučavano je građenje kompleksa kobalta(II) sa hloridnim i bromidnim jonima u rastopima koji sadrže jednu neorgansku so i jedno organsko jedinjenje i/ili vodu pri različitom sastavu sistema i na različitim temperaturama. Jedan od sistema je amonijum-nitrat – acetamid – voda sastava NH₄NO₃∙(2,61-z)CH₃CONH₂∙zH₂O (z = 0,0 1,61 i 2,61), a drugi sistem je amonijum–nitrat – dimetilsulfoksid (DMSO) sastava NH₄NO₃∙zDMSO (z = 1 – 6), na različitim temperaturama (35, 45, 55 i 65 ^oC). Cilj ovog istraživanja je bio određivanje stabilnosti kompleksa kobalta koji se grade sa sa halogenidnim jonima i komponentama rastvarača, pronalaženje kvalitativne i kvantitativne zavisnosti konstanti stabilnosti kompleksa kobalta(II) sa halogenidnim jonima od temperature i molskog odnosa komponenti sistema NH₄NO₃∙(2,61-z)CH₃CONH₂∙zH₂O odnosno NH₄NO₃∙zDMSO, određivanje termodinamičkih parametara koji karakterišu reakcije asocijacije u ovim sistemima.
In this dissertation the complex formation between cobalt(II) and halide ions in the melts consisting of one inorganic salt, an organic compound and/or water has been studied at different temperatures. Two molten salt systems have been investigated: 1) ammonium nitrate-acetamide-water system NH₄NO₃∙(2,61-z)CH₃CONH₂∙zH₂O (z = 0.0 1.61 2.61) and 2) ammonium nitratedimethyl sulfoxide NH₄NO₃∙zDMSO (z = 1 – 6), at four different temperatures: 35, 45, 55 and 65 ^oC. The purpose of this work was to determine stability of cobalt(II) complexes formed with the halide ions and the components of the solvents, to discribe the qualitative and quantitative relationships between the stability of the complexes and the melt composition, as well as the changes in the cobalt(II) coordination due to a complex formation. Thermodynamic parameters for cobalt(II) – halide association process in these melts were alsodetermined.

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劉汝這 et Yue-huen Thomas Lau. « Ultrastructural and stereological investigation of the effects of hexamethylene bisacetamide on human colon carcinoma LoVo cells invitro ». Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2000. http://hub.hku.hk/bib/B29872972.

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DRUOT, HOULLEMARE SOPHIE. « Influence des interactions homo- et heterochirales lors du dedoublement par cristallisation preferentielle de deux derives de l'alpha-methylbenzylamine : le n-acetamide et le chloroacetate ». Caen, 1999. http://www.theses.fr/1999CAEN2029.

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Une etude comparative du dedoublement par cristallisation preferentielle classique et auto-ensemencee des derives chloroacetate et n-acetyl de l'-methylbenzylamine est realisee. Les resultats sont largement inferieurs aux maxima autorises par la thermodynamique. L'etude detaillee des diagrammes binaires revele l'existence de compose racemique instable dans le premier cas ou metastable pour le n-acetyl. Il est montre que les interactions heterochirales peuvent inhiber la croissance selective d'un enantiomere dans une solution quasi racemique. Dans le cas du chloroacetate, des experiences de re-croissance cristalline en solution aqueuse enantiomeriquement pure montrent de plus une totale dissymetrie de reconstruction des monocristaux liee a un effet de solvant.

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Meilhoc, Eliane. « Polyamines et differenciation induite par l'hexamethylene bis acetamide (hmba) de cellules erythroleucemiques de souris : role cle de la desacetylation de l'hmba dans cette differenciation ». Clermont-Ferrand 2, 1986. http://www.theses.fr/1986CLF2D177.

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De nombreuses modifications membranaires, cytoplasmiques et nucleaires accompagnent ce processus de differenciation induite. La question fondamentale qui se pose est de savoir, lesquelles, parmi ces modifications sont necessaires a la differenciation des cellules de friend. Peu d'elements permettent d'y repondre actuellement. Nos travaux montrent que des changements dans le metabolisme des polyamines (baisse de l'activite de l'ornithine decarboxylase et des taux intracellulaires en putrescine et spermidine) sont necessaires a la differenciation induite des cellules de friend. Une ou plusieurs etapes dependantes de polyamines interviendraient tres tot dans le deroulement du processus de differenciation. Par ailleurs, les modifications du metabolisme des polyamines sont correlees avec l'accumulation des produits de desacetylation intracellulaire de l'hmba (n-acetyl-diamino-1,6-hexane et diamino-1,6-hexane)

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Conley, Matthew. « Supercritical Water Gasification of Two-Carbon Carboxylic Acid Derivatives ». Ohio University / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1542202432022198.

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Livres sur le sujet "Acetamide"

Scribner, Elisabeth A. Acetamide herbicides and their degradation products in ground water and surface water of the United States, 1993-2003. Reston, Va : U.S. Department of the Interior, U.S. Geological Survey, 2004.

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Tou, Grace. The pharmacokinetics of 2-acetamido-P-cresol and the effects of deacetylation on its toxicodynamics. Ottawa : National Library of Canada, 1991.

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Wardle, N. J. Syntheses and characterisation of novel 1-acetamido-2,2-biscarbamyl-ethanephosphonate derivatives. 1998.

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Michnick, Thomas John. Asymmetric synthesis of acetamido boronic acids and asymmetric synthesis using boronic esters. 1990.

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Tou, Grace. The pharmacokinetics of 2-acetamido-P-cresol and the effects of deacetylation on its toxicodynamics. 1991.

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Chapitres de livres sur le sujet "Acetamide"

Gooch, Jan W. « Acetamide ». Dans Encyclopedic Dictionary of Polymers, 8. New York, NY : Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_101.

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Irvine, William. « Acetamide ». Dans Encyclopedia of Astrobiology, 1. Berlin, Heidelberg : Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-642-27833-4_5321-1.

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Irvine, William M. « Acetamide ». Dans Encyclopedia of Astrobiology, 46–47. Berlin, Heidelberg : Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65093-6_5321.

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Gooch, Jan W. « Dimethyl Acetamide ». Dans Encyclopedic Dictionary of Polymers, 226. New York, NY : Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_3707.

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Gooch, Jan W. « Hydroxyethyl Acetamide ». Dans Encyclopedic Dictionary of Polymers, 377. New York, NY : Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_6156.

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Bährle-Rapp, Marina. « Acetamide MEA ». Dans Springer Lexikon Kosmetik und Körperpflege, 4. Berlin, Heidelberg : Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_56.

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Gooch, Jan W. « N-Methyl Acetamide ». Dans Encyclopedic Dictionary of Polymers, 456. New York, NY : Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_7388.

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Demaison, J. « 211 C2H5NO Acetamide ». Dans Asymmetric Top Molecules. Part 1, 412–13. Berlin, Heidelberg : Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-10371-1_213.

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Simola, Nicola, Micaela Morelli, Tooru Mizuno, Suzanne H. Mitchell, Harriet de Wit, H. Valerie Curran, Celia J. A. Morgan et al. « 2-[(Diphenylmethyl)Sulfinyl]acetamide ». Dans Encyclopedia of Psychopharmacology, 405. Berlin, Heidelberg : Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_3009.

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Mizuno, Tooru M., Ashwini Padhi, Naomi Fineberg, Naomi A. Fineberg, Ashwini Padhi, Michael H. Bloch, James F. Leckman et al. « 2-Oxopyrrolidin-1-Acetamide ». Dans Encyclopedia of Psychopharmacology, 944. Berlin, Heidelberg : Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_4014.

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Actes de conférences sur le sujet "Acetamide"

Ilyushin, Vadim, Ruslan Porohovoi, Eugene Alekseev, Mykola Pogrebnyak, Holger S. P. Muller, Frank Lewen et Stephan Schlemmer. « The Third Excited Torsional State of Acetamide ». Dans 2022 IEEE 2nd Ukrainian Microwave Week (UkrMW). IEEE, 2022. http://dx.doi.org/10.1109/ukrmw58013.2022.10037019.

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Coudert, L., J. C. Guillemin, H. Møllendal, R. Motiyenko, L. Margulès, T. Huet, C. Gutle et I. Konov. « THE MICROWAVE SPECTRUM OF MONODEUTERATED ACETAMIDE CH2DC(=O)NH2 ». Dans 69th International Symposium on Molecular Spectroscopy. Urbana, Illinois : University of Illinois at Urbana-Champaign, 2014. http://dx.doi.org/10.15278/isms.2014.fa07.

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Srinivasan, H., P. S. Dubey, V. K. Sharma, R. Biswas, S. Mitra et R. Mukhopadhyay. « Molecular dynamics of acetamide based ionic deep eutectic solvents ». Dans DAE SOLID STATE PHYSICS SYMPOSIUM 2017. Author(s), 2018. http://dx.doi.org/10.1063/1.5029015.

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Prathap, S., et J. Madhavan. « Synthesis, experimental and theoretical investigations of N-(3-nitrophenyl) acetamide (3NAA) ». Dans SOLID STATE PHYSICS : Proceedings of the 56th DAE Solid State Physics Symposium 2011. AIP, 2012. http://dx.doi.org/10.1063/1.4710488.

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CHENG, YUCHUAN, JIANJUN GUO, XUEHUI LIU, GAOJIE XU et PING CUI. « PREPARATION AND ELECTRORHEOLOGICAL EFFECT OF ACETAMIDE-MODIFIED TITANATE NANOTUBE SUSPENSIONS INSTRUCTIONS ». Dans Proceedings of the 12th International Conference. WORLD SCIENTIFIC, 2011. http://dx.doi.org/10.1142/9789814340236_0054.

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Hemaraju, B. C., B. S. Madhukar, D. G. Bhadregowda et A. P. Gnana Prakash. « Growth and characterization of new organic nonlinear optical crystal (R)-2-cyano-N-(1-phenylethyl) acetamide ». Dans SOLID STATE PHYSICS : Proceedings of the 58th DAE Solid State Physics Symposium 2013. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4873089.

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Kumar, Rohitash, Ravindra Kumar et Ambesh Dixit. « Thermal phase diagram of acetamide-benzoic acid and benzoic acid-phthalimide binary systems for solar thermal applications ». Dans INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC 2015) : Proceeding of International Conference on Condensed Matter and Applied Physics. Author(s), 2016. http://dx.doi.org/10.1063/1.4946738.

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Asmatulu, R., S. Davluri et W. Khan. « Fabrications of CNT Based Nanocomposite Fibers From the Recycled Plastics ». Dans ASME 2009 International Mechanical Engineering Congress and Exposition. ASMEDC, 2009. http://dx.doi.org/10.1115/imece2009-12338.

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Electrospinning is a viable technique that spins fibers at different diameters starting from 3 nm to several micron meters. This technique allows the fabrication of random and aligned fibers of diverse structures, such as ribbon or cylindrical shapes. In this work, the spinning solution is prepared by dissolving recycled polystyrene and the mixture of polystyrene and polyvinyl chloride along with carbon nanotubes in dimethyl acetamide (DMAc). The dispersions were then electrospun at various DC voltage, pump speed, concentration and distance. The general morphology of the fibers has been studied by scanning electron microscopy (SEM). The test results confirmed that fiber diameter and surface roughness were increased by increasing the CNTs, which may be because of the viscosity increase of the spinning solution. Addition of carbon nanotubes in the polymer solution also improves the thermal and electrical conductivity, as well as toughness, stiffness and other properties.

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El Rayes, S. M. « Convenient synthesis of some methyl-N-[2-(6-oxo-3-p-tolyl-5,6-dihydro-4H-pyridazin-1-yl)-acetamide]alkanoates ». Dans The 12th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland : MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01204.

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El Rayes, S. « Convenient synthesis of some methyl-N-[2-(6-oxo-3-p-tolyl-5,6-dihydro-4H-pyridazin-1-yl)-acetamide]alkanoates ». Dans The 12th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland : MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01228.

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Rapports d'organisations sur le sujet "Acetamide"

Firman, Paul, Edward M. Eyring, Meizhen Xu, Andrea Marchetti et Sergio Petrucci. Static, Microwave, Infrared, and Visible Permittivity Related to chemical Structure : N-Methylacetamide, N-dimethyl Acetamide and their Mixtures in CCl4 at 32 Deg. C. Fort Belvoir, VA : Defense Technical Information Center, juin 1991. http://dx.doi.org/10.21236/ada246364.

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