Home Halogens Epibromohydrin

Epibromohydrin

CAS No.:
3132-64-7
Catalog Number:
AG0037NR
Molecular Formula:
C3H5BrO
Molecular Weight:
136.9752
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
Product Description
Catalog Number:
AG0037NR
Chemical Name:
Epibromohydrin
CAS Number:
3132-64-7
Molecular Formula:
C3H5BrO
Molecular Weight:
136.9752
MDL Number:
MFCD00005130
IUPAC Name:
2-(bromomethyl)oxirane
InChI:
InChI=1S/C3H5BrO/c4-1-3-2-5-3/h3H,1-2H2
InChI Key:
GKIPXFAANLTWBM-UHFFFAOYSA-N
SMILES:
BrCC1CO1
EC Number:
221-525-3
NSC Number:
630
UN Number:
2558
Properties
Complexity:
37.9  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
135.952g/mol
Formal Charge:
0
Heavy Atom Count:
5  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
136.976g/mol
Monoisotopic Mass:
135.952g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
12.5A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
0.8  
Literature
Title Journal
Reactivity of activated versus nonactivated 2-(bromomethyl)aziridines with respect to sodium methoxide: a combined computational and experimental study. The Journal of organic chemistry 20111104
A Pseudomonas aeruginosa toxin that hijacks the host ubiquitin proteolytic system. PLoS pathogens 20110301
Alkyltransferase-mediated toxicity of bis-electrophiles in mammalian cells. Mutation research 20100203
Synthesis and antimalarial evaluation of some 4-quinazolinone derivatives based on febrifugine. Journal of advanced pharmaceutical technology & research 20100101
Effect of O6-alkylguanine-DNA alkyltransferase on genotoxicity of epihalohydrins. Environmental and molecular mutagenesis 20090701
Quantitative PCR analysis of diepoxybutane and epihalohydrin damage to nuclear versus mitochondrial DNA. Mutation research 20090512
Synthesis of triazole-oxazolidinones via a one-pot reaction and evaluation of their antimicrobial activity. Bioorganic & medicinal chemistry letters 20080901
DNA interstrand cross-linking by epichlorohydrin. Chemical research in toxicology 20070501
Quantitative structure-activity relationships for toxicity and genotoxicity of halogenated aliphatic compounds: wing spot test of Drosophila melanogaster. Chemosphere 20070201
Reactions of glycidyl derivatives with ambident nucleophiles; part 2: amino acid derivatives. Beilstein journal of organic chemistry 20070101
One-pot cyclizations of dilithiated oximes and hydrazones with epibromohydrin. Efficient synthesis of 6-hydroxymethyl-5,6-dihydro-4H-1,2-oxazines and oxazolo[3,4-b]pyridazin-7-ones. The Journal of organic chemistry 20060317
Chemo-, regio-, and diastereoselective synthesis of functionalized cyclopropanes by cyclization of dilithiated nitriles with epibromohydrin. Organic letters 20011129
Regio- and stereoselective synthesis of Nor-nonactinic acid derivatives--kinetic reaction control in the Lewis acid mediated domino reaction of 1,3-dicarbonyl dianions with 1-bromo-2,3-epoxypropanes. Chemistry (Weinheim an der Bergstrasse, Germany) 20010202
The x-ray structure of epoxide hydrolase from Agrobacterium radiobacter AD1. An enzyme to detoxify harmful epoxides. The Journal of biological chemistry 19990521
Characterization of a novel enantioselective halohydrin hydrogen-halide-lyase. Applied and environmental microbiology 19940401
Properties