Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C2H4BrNO |
| Molecular Weight | 137.963 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)NBr
InChI
InChIKey=VBTQNRFWXBXZQR-UHFFFAOYSA-N
InChI=1S/C2H4BrNO/c1-2(5)4-3/h1H3,(H,4,5)
| 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
| Title | Date | PubMed |
|---|---|---|
| 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 Feb 18 |
|
| 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 Jun 29 |
|
| 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 Feb 27 |
|
| K3PO4-catalyzed regiospecific aminobromination of beta-nitrostyrene derivatives with N-bromoacetamide as aminobrominating agent. | 2010 Mar 19 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:36:15 GMT 2023
by
admin
on
Sat Dec 16 09:36:15 GMT 2023
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| Record UNII |
0AQ6MWH7ZB
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| Record Status |
Validated (UNII)
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| Record Version |
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C016272
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79-15-2
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m2675
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0AQ6MWH7ZB
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DTXSID5024633
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201-181-0
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4353
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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SOLVATE->ANHYDROUS |
