301272
2-Bromoacetamide
98%
Sinónimos:
α-Bromoacetamide
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Acerca de este artículo
Fórmula lineal:
BrCH2CONH2
Número CAS:
Peso molecular:
137.96
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1739073
Assay:
98%
Servicio técnico
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Permítanos ayudarleQuality Level
assay
98%
mp
87-91 °C (lit.)
functional group
amide, bromo
SMILES string
NC(=O)CBr
InChI
1S/C2H4BrNO/c3-1-2(4)5/h1H2,(H2,4,5)
InChI key
JUIKUQOUMZUFQT-UHFFFAOYSA-N
General description
Kinetics of reaction of 2-bromoacetamide with a 39 base pair duplex DNA sequence was studied.
Application
2-Bromoacetamide was used in preparation of (2-carbamoylmethoxy-5-chloro-benzyl)-carbamic acid tert-butyl ester. It was aslo used as precursor to dehydropeptidase I inactivator.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B
Clase de almacenamiento
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Targeting renal dipeptidase (dehydropeptidase I) for inactivation by mechanism-based inactivators.
Y Q Wu et al.
Journal of medicinal chemistry, 34(6), 1914-1916 (1991-06-01)
Shunke Ding et al.
Water research, 143, 325-333 (2018-07-10)
The effective removal of haloacetamides (HAMs) as a group of emerging disinfection by-products is essential for drinking water safety. This study investigated the degradation of 10 HAMs, including chlorinated, brominated, and iodinated analogues, by sodium sulfite (S(IV)) and the mechanism
Ni Cheng et al.
Journal of colloid and interface science, 511, 215-221 (2017-10-14)
Studies on supramolecular gel aggregates via supramolecular interactions are very fascinating and impressive. The interactions of gelator with solvent and inorganic salt can functionalize, activate, or control the properties of supramolecular gels. A lot of work on this area has