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150703

Sigma-Aldrich

Acetamide

zone-refined, purified by sublimation, 99%

Synonym(s):

Amide C2

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About This Item

Linear Formula:
CH3CONH2
CAS Number:
Molecular Weight:
59.07
Beilstein/REAXYS Number:
1071207
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

grade

zone-refined

vapor pressure

1 mmHg ( 65 °C)

assay

99%

form

solid

purified by

sublimation

bp

221 °C (lit.)

mp

78-80 °C (lit.)

SMILES string

CC(N)=O

InChI

1S/C2H5NO/c1-2(3)4/h1H3,(H2,3,4)

InChI key

DLFVBJFMPXGRIB-UHFFFAOYSA-N

Gene Information

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pictograms

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signalword

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hcodes

Hazard Classifications

Carc. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


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Asal Fallah-Tafti et al.
European journal of medicinal chemistry, 46(10), 4853-4858 (2011-08-20)
KX2-391 (KX-01/Kinex Pharmaceuticals), N-benzyl-2-(5-(4-(2-morpholinoethoxy)phenyl)pyridin-2-yl)acetamide, is a highly selective Src substrate binding site inhibitor. To understand better the role of pyridine ring and N-benzylsubstitution in KX2-391 and establish the structure-activity relationship, a number of N-benzyl substituted (((2-morpholinoethoxy)phenyl)thiazol-4-yl)acetamide derivatives containing thiazole instead
E C B Silva et al.
Animal reproduction science, 132(3-4), 155-158 (2012-06-26)
The aim was to assess the in vitro effect of glycerol, ethylene glycol or acetamide on frozen-thawed ram spermatozoa. Aliquots of each sixteen ejaculates from four rams of the Morada Nova breed were diluted in Tris-egg yolk with glycerol (5%)
A Subha Mahadevi et al.
Physical chemistry chemical physics : PCCP, 13(33), 15211-15220 (2011-07-16)
Insights into the formation of hydrogen bonded clusters are of outstanding importance and quantum chemical calculations play a pivotal role in achieving this understanding. Structure and energetic comparison of linear, circular and standard forms of (acetamide)(n) clusters (n = 1-15)
Jie Guang et al.
Organic letters, 14(12), 3174-3177 (2012-06-02)
Highly enantioselective aldol reactions of acetylphosphonates and activated carbonyl compounds was realized with cinchona alkaloid derived catalysts, in which the acetylphosphonate was directly used as an enolate precursor for the first time. The aldol product obtained was converted in situ
Lingle Wang et al.
Proceedings of the National Academy of Sciences of the United States of America, 109(6), 1937-1942 (2012-02-07)
We apply a free energy perturbation simulation method, free energy perturbation/replica exchange with solute tempering, to two modifications of protein-ligand complexes that lead to significant conformational changes, the first in the protein and the second in the ligand. The approach

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