75434
Acetamide
≥98.0% (GC)
Sinónimos:
Amide C2
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Acerca de este artículo
Fórmula lineal:
CH3CONH2
Número CAS:
Peso molecular:
59.07
EC Number:
200-473-5
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
1071207
MDL number:
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Servicio técnico
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Permítanos ayudarlevapor pressure
1 mmHg ( 65 °C)
assay
≥98.0% (GC)
form
crystals
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
rat ... Ggt1(116568)
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signalword
Warning
hcodes
Hazard Classifications
Carc. 2
Clase de almacenamiento
11 - Combustible Solids
wgk
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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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