Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | CH2BrNO2 |
| Molecular Weight | 139.936 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[O-][N+](=O)CBr
InChI
InChIKey=DNPRVXJGNANVCZ-UHFFFAOYSA-N
InChI=1S/CH2BrNO2/c2-1-3(4)5/h1H2
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Umpolung reactivity in amide and peptide synthesis. | 2010-06-24 |
|
| Free-radical chemistry of disinfection byproducts. 3. Degradation mechanisms of chloronitromethane, bromonitromethane, and dichloronitromethane. | 2010-01-14 |
|
| Genotoxic evaluation of two halonitromethane disinfection by-products in the Drosophila wing-spot test. | 2009-05 |
|
| Genotoxicity analysis of two halonitromethanes, a novel group of disinfection by-products (DBPs), in human cells treated in vitro. | 2009-04 |
|
| Enantioselective synthesis of functionalized nitrocyclopropanes by organocatalytic conjugate addition of bromonitroalkanes to alpha,beta-unsaturated enones. | 2009 |
|
| A catalytic highly enantioselective direct synthesis of 2-bromo-2-nitroalkan-1-ols through a Henry reaction. | 2008-10-21 |
|
| Stereoselective NaN3-catalyzed halonitroaldol-type reaction of azetidine-2,3-diones in aqueous media. | 2008-05-07 |
|
| Efficient addition reaction of bromonitromethane to aldehydes catalyzed by NaI: a new route to 1-bromo-1-nitroalkan-2-ols under very mild conditions. | 2006-12-21 |
|
| Efficient nitro-aldol reaction using SmI2: a new route to nitro alcohols under very mild conditions. | 2006-09-29 |
|
| Free radical chemistry of disinfection-byproducts. 1. Kinetics of hydrated electron and hydroxyl radical reactions with halonitromethanes in water. | 2006-02-16 |
|
| Mutagenicity in Salmonella of halonitromethanes: a recently recognized class of disinfection by-products in drinking water. | 2004-08-08 |
|
| Halonitromethane drinking water disinfection byproducts: chemical characterization and mammalian cell cytotoxicity and genotoxicity. | 2004-01-01 |
Patents
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Preferred Name | English | ||
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Systematic Name | English | ||
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DTXSID7060338
Created by
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68423
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C533588
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EG63P9EUR0
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209-258-0
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563-70-2
Created by
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SUBSTANCE RECORD
