(2-Bromoethyl)benzene

General

Type :

Chemical_Nomenclature : 2-bromoethylbenzene

Canonical SMILES : C1=CC=C(C=C1)CCBr

InChI : InChI=1S\/C8H9Br\/c9-7-6-8-4-2-1-3-5-8\/h1-5H,6-7H2

InChIKey : WMPPDTMATNBGJN-UHFFFAOYSA-N

Other name(s) : Phenethyl bromide  ||  2-Bromoethylbenzene  ||  2-Phenylethyl bromide  ||  (2-bromo)ethanebenzene  ||  SCHEMBL1552  ||  1-(2-bromo-ethyl)-benzene  ||  CHEMBL1340745


MW : 185.06

Formula : C8H9Br

CAS_number : 103-63-9

PubChem : 7666

UniChem : WMPPDTMATNBGJN-UHFFFAOYSA-N

Target

Structures : No structure

Families : Epoxide_hydrolase

References (2)

Title : High-throughput selection of (new) enzymes: phage display-mediated isolation of alkyl halide hydrolases from a library of active-site mutated epoxide hydrolases - Blazic_2024_Faraday.Discuss__
Author(s) : Blazic M , Gautier C , Norberg T , Widersten M
Ref : Faraday Discussion , : , 2024
Abstract :
PubMedSearch : Blazic_2024_Faraday.Discuss__
PubMedID: 38828992
Gene_locus related to this paper: soltu-3epoxy

Title : Chlorogenate hydrolase-catalyzed synthesis of hydroxycinnamic acid ester derivatives by transesterification, substitution of bromine, and condensation reactions - Kishimoto_2005_Appl.Microbiol.Biotechnol_68_198
Author(s) : Kishimoto N , Kakino Y , Iwai K , Fujita T
Ref : Applied Microbiology & Biotechnology , 68 :198 , 2005
Abstract :
PubMedSearch : Kishimoto_2005_Appl.Microbiol.Biotechnol_68_198
PubMedID: 15717173