Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C3H5BrO |
| Molecular Weight | 136.975 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
BrCC1CO1
InChI
InChIKey=GKIPXFAANLTWBM-UHFFFAOYSA-N
InChI=1S/C3H5BrO/c4-1-3-2-5-3/h3H,1-2H2
| Molecular Formula | C3H5BrO |
| Molecular Weight | 136.975 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Characterization of a novel enantioselective halohydrin hydrogen-halide-lyase. | 1994 Apr |
|
| The x-ray structure of epoxide hydrolase from Agrobacterium radiobacter AD1. An enzyme to detoxify harmful epoxides. | 1999 May 21 |
|
| Chemo-, regio-, and diastereoselective synthesis of functionalized cyclopropanes by cyclization of dilithiated nitriles with epibromohydrin. | 2001 Nov 29 |
|
| Synthesis of triazole-oxazolidinones via a one-pot reaction and evaluation of their antimicrobial activity. | 2008 Sep 1 |
|
| Quantitative PCR analysis of diepoxybutane and epihalohydrin damage to nuclear versus mitochondrial DNA. | 2009 May 12 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 07:53:59 GMT 2023
by
admin
on
Sat Dec 16 07:53:59 GMT 2023
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| Record UNII |
8E89677I6B
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| Record Status |
Validated (UNII)
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| Record Version |
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