Home Bromides 563-70-2
563-70-2,MFCD00007401
Catalog No.:AA0034HQ

563-70-2 | Bromonitromethane

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1g
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$113.00   $79.00
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5g
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA0034HQ
Chemical Name:
Bromonitromethane
CAS Number:
563-70-2
Molecular Formula:
CH2BrNO2
Molecular Weight:
139.9361
MDL Number:
MFCD00007401
SMILES:
BrCN(=O)=O
Properties
Properties
 
BP:
147.5°C at 760 mmHg  
Form:
Liquid  
Refractive Index:
1.485-1.495  
Storage:
Keep in dry area;Room Temperature;  

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

Literature

Title: Enantioselective synthesis of α-oxy amides via Umpolung amide synthesis.

Journal: Journal of the American Chemical Society 20120919

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

Journal: Chemical research in toxicology 20111219

Title: Determination of halonitromethanes in treated water.

Journal: Journal of chromatography. A 20110506

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

Journal: Environmental pollution (Barking, Essex : 1987) 20110201

Title: Umpolung reactivity in amide and peptide synthesis.

Journal: Nature 20100624

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

Journal: The journal of physical chemistry. A 20100114

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

Journal: Chemosphere 20090501

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

Journal: Environmental research 20090401

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

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20090101

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

Journal: Chemical communications (Cambridge, England) 20081021

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

Journal: Organic & biomolecular chemistry 20080507

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

Journal: Organic letters 20061221

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

Journal: The Journal of organic chemistry 20060929

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

Journal: The journal of physical chemistry. A 20060216

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

Journal: Mutation research 20040808

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

Journal: Environmental science & technology 20040101

Title: Dawn M Makley, et al. Silyl Imine Electrophiles in Enantioselective Catalysis: A Rosetta Stone for Peptide Homologation, Enabling Diverse N-protected Aryl Glycines From Aldehydes in Three Steps. Org Lett. 2014 Jun 6;16(11):3146-9.

Title: Alicia Marsà, et al. In Vitro Studies on the Tumorigenic Potential of the Halonitromethanes Trichloronitromethane and Bromonitromethane. Toxicol In Vitro. 2017 Dec;45(Pt 1):72-80.

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