EPIBROMOHYDRIN

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

Structure Search

SMILES

BrCC1CO1

InChI

InChIKey=GKIPXFAANLTWBM-UHFFFAOYSA-N

InChI=1S/C3H5BrO/c4-1-3-2-5-3/h3H,1-2H2

HIDE SMILES / InChI

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
Synthesis and antimalarial evaluation of some 4-quinazolinone derivatives based on febrifugine.	2010-10	22247880
Alkyltransferase-mediated toxicity of bis-electrophiles in mammalian cells.	2010-02-03	19941875
Effect of O6-alkylguanine-DNA alkyltransferase on genotoxicity of epihalohydrins.	2009-07	19472322
Quantitative PCR analysis of diepoxybutane and epihalohydrin damage to nuclear versus mitochondrial DNA.	2009-05-12	19428380
Synthesis of triazole-oxazolidinones via a one-pot reaction and evaluation of their antimicrobial activity.	2008-09-01	18678487
Reactions of glycidyl derivatives with ambident nucleophiles; part 2: amino acid derivatives.	2007-09-27	17900352
DNA interstrand cross-linking by epichlorohydrin.	2007-05	17441735
Quantitative structure-activity relationships for toxicity and genotoxicity of halogenated aliphatic compounds: wing spot test of Drosophila melanogaster.	2007-02	17113125
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.	2006-03-17	16526776
Chemo-, regio-, and diastereoselective synthesis of functionalized cyclopropanes by cyclization of dilithiated nitriles with epibromohydrin.	2001-11-29	11720565
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.	2001-02-02	11261653
The x-ray structure of epoxide hydrolase from Agrobacterium radiobacter AD1. An enzyme to detoxify harmful epoxides.	1999-05-21	10329649
Characterization of a novel enantioselective halohydrin hydrogen-halide-lyase.	1994-04	8017917

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:45:03 GMT 2025` Edited by `admin` on `Mon Mar 31 21:45:03 GMT 2025`
Record UNII	8E89677I6B
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

NSC-630

Preferred Name

English

EPIBROMOHYDRIN

Common Name

English

OXIRANE, (BROMOMETHYL)-

Systematic Name

English

EPIBROMOHYDRIN, (±)-

Systematic Name

English

PROPANE, 1-BROMO-2,3-EPOXY-

Systematic Name

English

OXIRANE, 2-(BROMOMETHYL)-

Systematic Name

English

(BROMOMETHYL)OXIRANE, (±)-

Systematic Name

English

3-BROMO-1,2-EPOXYPROPANE, (±)-

Systematic Name

English

(BROMOMETHYL)OXIRANE

Systematic Name

English

OXIRANYLMETHYL BROMIDE

Systematic Name

English

(BROMOMETHYL)ETHYLENE OXIDE

Systematic Name

English

2-(BROMOMETHYL)OXIRANE

Systematic Name

English

BROMOHYDRIN

Common Name

English

2,3-EPOXYPROPYL BROMIDE

Systematic Name

English

EPIBROMOHYDRINE

Common Name

English

EPIBROMOHYDRIN [HSDB]

Common Name

English

1-BROMO-2,3-EPOXYPROPANE

Systematic Name

English

PROPANE, 3-BROMO-1,2-EPOXY-

Systematic Name

English

1,2-EPOXY-3-BROMOPROPANE

Systematic Name

English

EPOXY BROMOPROPANE

Systematic Name

English

3-BROMO-1,2-EPOXYPROPANE

Systematic Name

English

Code System Code Type Description

ECHA (EC/EINECS)

221-525-3