C0267
2-Chloroacetamide
≥98%
Synonym(s):
Chloracetamide, alpha-Chloroacetamide
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About This Item
Linear Formula:
ClCH2CONH2
CAS Number:
Molecular Weight:
93.51
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-174-2
Beilstein/REAXYS Number:
878191
MDL number:
Assay:
≥98%
Form:
powder
vapor pressure
0.05 mmHg ( 20 °C)
Quality Level
assay
≥98%
form
powder
mp
116-118 °C (lit.)
SMILES string
NC(=O)CCl
InChI
1S/C2H4ClNO/c3-1-2(4)5/h1H2,(H2,4,5)
InChI key
VXIVSQZSERGHQP-UHFFFAOYSA-N
General description
2-Chloroacetamide, also known as alpha-Chloroacetamide, is a chlorinated organic compound commonly used as a precursor in the synthesis of amides and thioamides.
Application
2-Chloroacetamidecan be used as a reactant to synthesize:
- 2-Amino-4-chloroquinolines via o-alkylation of 4-chloro-1H-quinolin-2-ones and subsequent Smiles rearrangement.
- 2-(Formylaryloxy)acetamides by reacting with hydroxybenzaldehydes in the presence of potassium carbonate as a base.
- Biarylamine derivatives via aluminum triflate-catalyzed direct amination of benzhydrols.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Repr. 2 - Skin Sens. 1
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 2
flash_point_f
338.0 °F
flash_point_c
170 °C
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Articles
Rapid trypsin digest kit yields reliable results in less than 2 hours for mass spectrometry analysis.
Cleonice Rocha et al.
Environmental pollution (Barking, Essex : 1987), 152(1), 239-244 (2007-07-17)
Solid-phase microextraction coupled with gas chromatography-mass spectrometry (SPME-GC-MS) was used to analyze two triazine (atrazine and simazine) and three chloroacetamide herbicides (acetochlor, alachlor, and metolachlor) in water samples from a midwest US agricultural drainage ditch for two growing seasons. The
Jun Zhang et al.
Journal of agricultural and food chemistry, 59(9), 4614-4621 (2011-03-23)
A butachlor-degrading strain, designated FLY-8, was isolated from rice field soil and was identified as Paracoccus sp. Strain FLY-8 could degrade and utilize six chloroacetamide herbicides as carbon sources for growth, and the degradation rates followed the order alachlor >
Felix Boos et al.
Nature cell biology, 21(4), 442-451 (2019-03-20)
The cytosolic accumulation of mitochondrial precursors is hazardous to cellular fitness and is associated with a number of diseases. However, it is not observed under physiological conditions. Individual mechanisms that allow cells to avoid cytosolic accumulation of mitochondrial precursors have
Global Trade Item Number
| SKU | GTIN |
|---|---|
| C0267-100G | 04061833450369 |
| C0267-1KG | 04061833450376 |
| C0267-500G | 04061833450383 |