563-70-2 | Bromonitromethane

Packsize	Purity	Availability	Price	Discounted Price
1g	90%	in stock	$114.00	$80.00
5g	90%	in stock	$300.00	$210.00

Description

• Catalog Number: AB45690
• Chemical Name: Bromonitromethane
• CAS Number: 563-70-2
• Molecular Formula: CH2BrNO2
• Molecular Weight: 139.9361
• MDL Number: MFCD00007401
• SMILES: BrCN(=O)=O

Computed Properties

• Complexity: 39.4
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 5
• Hydrogen Bond Acceptor Count: 2
• XLogP3: 0.9

Literature

• Enantioselective synthesis of α-oxy amides via Umpolung amide synthesis.

  Journal of the American Chemical Society 20120919

• Evidence for chemical and cellular reactivities of the formaldehyde releaser bronopol, independent of formaldehyde release.

  Chemical research in toxicology 20111219

• Determination of halonitromethanes in treated water.

  Journal of chromatography. A 20110506

• Toxicity profile of labile preservative bronopol in water: the role of more persistent and toxic transformation products.

  Environmental pollution (Barking, Essex : 1987) 20110201

• Umpolung reactivity in amide and peptide synthesis.

  Nature 20100624

• Free-radical chemistry of disinfection byproducts. 3. Degradation mechanisms of chloronitromethane, bromonitromethane, and dichloronitromethane.

  The journal of physical chemistry. A 20100114

• Genotoxic evaluation of two halonitromethane disinfection by-products in the Drosophila wing-spot test.

  Chemosphere 20090501

• Genotoxicity analysis of two halonitromethanes, a novel group of disinfection by-products (DBPs), in human cells treated in vitro.

  Environmental research 20090401

• Enantioselective synthesis of functionalized nitrocyclopropanes by organocatalytic conjugate addition of bromonitroalkanes to alpha,beta-unsaturated enones.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20090101

• A catalytic highly enantioselective direct synthesis of 2-bromo-2-nitroalkan-1-ols through a Henry reaction.

  Chemical communications (Cambridge, England) 20081021

• Stereoselective NaN3-catalyzed halonitroaldol-type reaction of azetidine-2,3-diones in aqueous media.

  Organic & biomolecular chemistry 20080507

• Efficient addition reaction of bromonitromethane to aldehydes catalyzed by NaI: a new route to 1-bromo-1-nitroalkan-2-ols under very mild conditions.

  Organic letters 20061221

• Efficient nitro-aldol reaction using SmI2: a new route to nitro alcohols under very mild conditions.

  The Journal of organic chemistry 20060929

• Free radical chemistry of disinfection-byproducts. 1. Kinetics of hydrated electron and hydroxyl radical reactions with halonitromethanes in water.

  The journal of physical chemistry. A 20060216

• Mutagenicity in Salmonella of halonitromethanes: a recently recognized class of disinfection by-products in drinking water.

  Mutation research 20040808

• Halonitromethane drinking water disinfection byproducts: chemical characterization and mammalian cell cytotoxicity and genotoxicity.

  Environmental science & technology 20040101