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Details

Stereochemistry ACHIRAL
Molecular Formula C2H4BrNO.H2O
Molecular Weight 155.979
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-BROMOACETAMIDE MONOHYDRATE

SMILES

O.CC(=O)NBr

InChI

InChIKey=URALNCAFCAQWHI-UHFFFAOYSA-N
InChI=1S/C2H4BrNO.H2O/c1-2(5)4-3;/h1H3,(H,4,5);1H2

HIDE SMILES / InChI

Molecular Formula H2O
Molecular Weight 18.0153
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C2H4BrNO
Molecular Weight 137.963
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
K3PO4-catalyzed regiospecific aminobromination of beta-nitrostyrene derivatives with N-bromoacetamide as aminobrominating agent.
2010-03-19
Pd(II)-catalysed and Hg(II)-co-catalysed oxidation of D-glucose and D-fructose by N-bromoacetamide in the presence of perchloric acid: a kinetic and mechanistic study.
2006-02-27
Probing the mechanism of hamster arylamine N-acetyltransferase 2 acetylation by active site modification, site-directed mutagenesis, and pre-steady state and steady state kinetic studies.
2004-06-29
Chemoselective ligation applied to the synthesis of a biantennary N-linked glycoform of CD52.
2003-05-21
Kinetics and mechanism of Ru(III) and Hg(II) co-catalyzed oxidation of D-galactose and D-ribose by N-bromoacetamide in perchloric acid.
2002-02-18
Chemoselective elaboration of O-linked glycopeptide mimetics by alkylation of 3-thioGalNAc.
2001-02-28
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:45:04 GMT 2025
Edited
by admin
on Mon Mar 31 22:45:04 GMT 2025
Record UNII
S2HYZ042S6
Record Status Validated (UNII)
Record Version
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Name Type Language
N-BROMOACETAMIDE MONOHYDRATE
MI  
Systematic Name English
N-BROMOACETAMIDE MONOHYDRATE [MI]
Preferred Name English
ACETAMIDE, N-BROMO-, MONOHYDRATE
Systematic Name English
Code System Code Type Description
FDA UNII
S2HYZ042S6
Created by admin on Mon Mar 31 22:45:04 GMT 2025 , Edited by admin on Mon Mar 31 22:45:04 GMT 2025
PRIMARY
CAS
5798-70-9
Created by admin on Mon Mar 31 22:45:04 GMT 2025 , Edited by admin on Mon Mar 31 22:45:04 GMT 2025
PRIMARY
PUBCHEM
55212072
Created by admin on Mon Mar 31 22:45:04 GMT 2025 , Edited by admin on Mon Mar 31 22:45:04 GMT 2025
PRIMARY
MERCK INDEX
m2675
Created by admin on Mon Mar 31 22:45:04 GMT 2025 , Edited by admin on Mon Mar 31 22:45:04 GMT 2025
PRIMARY Merck Index
Related Record Type Details
ANHYDROUS->SOLVATE