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695122
Acetamid
sublimed, 99%
Synonym(e):
Amid C2
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About This Item
Lineare Formel:
CH3CONH2
CAS-Nummer:
Molekulargewicht:
59.07
Beilstein:
1071207
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
Empfohlene Produkte
Dampfdruck
1 mmHg ( 65 °C)
Qualitätsniveau
Assay
99%
Form
sublimed
bp
221 °C (lit.)
mp (Schmelzpunkt)
78-80 °C (lit.)
Funktionelle Gruppe
amide
SMILES String
CC(N)=O
InChI
1S/C2H5NO/c1-2(3)4/h1H3,(H2,3,4)
InChIKey
DLFVBJFMPXGRIB-UHFFFAOYSA-N
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Verwandte Kategorien
Signalwort
Warning
H-Sätze
Gefahreneinstufungen
Carc. 2
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 1
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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Cristian Varela et al.
Chemistry & biology, 19(4), 498-506 (2012-04-24)
Mycolic acids are vital components of the cell wall of the tubercle bacillus Mycobacterium tuberculosis and are required for viability and virulence. While mycolic acid biosynthesis is studied extensively, components involved in mycolate transport remain unidentified. We investigated the role
A E Alves et al.
Reproduction in domestic animals = Zuchthygiene, 47(6), 1003-1008 (2012-03-06)
This study was undertaken to compare cryotolerance, in terms of viability and resumption of meiosis after warming and culture (24 and 48 h), of ex situ (isolated) and in situ (enclosed in the ovarian tissue) feline cumulus-oocyte complexes (COCs) vitrified
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
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
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