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301272

Sigma-Aldrich

2-Bromoacetamide

98%

Sinonimo/i:

α-Bromoacetamide

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About This Item

Formula condensata:
BrCH2CONH2
Numero CAS:
683-57-8
Peso molecolare:
137.96
Beilstein:
1739073
Numero MDL:
MFCD00008025
Codice UNSPSC:
12352100
ID PubChem:
24858176
NACRES:
NA.22

Livello qualitativo

200

Saggio

98%

Punto di fusione

87-91 °C (lit.)

Gruppo funzionale

amide
bromo

Stringa SMILE

NC(=O)CBr

InChI

1S/C2H4BrNO/c3-1-2(4)5/h1H2,(H2,4,5)
JUIKUQOUMZUFQT-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

Kinetics of reaction of 2-bromoacetamide with a 39 base pair duplex DNA sequence was studied.

Applicazioni

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.

Pittogrammi

Skull and crossbonesCorrosion
GHS06,GHS05

Avvertenze

Danger

Indicazioni di pericolo

H301,H314

Classi di pericolo

Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B

Codice della classe di stoccaggio

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
BCCF9839
BCBV3517
1451937V
1451936V
1451937

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Sigma-Aldrich

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Sigma-Aldrich

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1,2,3-Trimethylbenzene analytical standard

Supelco

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Sigma-Aldrich

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Sigma-Aldrich

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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
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)
M J Taylor et al.
Bioconjugate chemistry, 8(3), 354-364 (1997-05-01)
Attachment of a nondiffusible bromoacetyl electrophile to the 5-position of a thymine at the 5'-end of a pyrimidine oligodeoxyribonucleotide affords sequence-specific alkylation of a guanine base in duplex DNA two base pairs to the 5'-side of a local triple-helical complex.
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
Yunkun Qian et al.
Water research, 186, 116346-116346 (2020-09-01)
Haloacetonitriles (HANs) and haloacetamides (HAMs) are nitrogenous disinfection byproducts that are present in filter backwash water (FBW) and sedimentation sludge water (SSW). In many cases FBW and SSW are recycled to the head of drinking water treatment plants. HAN and
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