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Details

Stereochemistry ACHIRAL
Molecular Formula C7H7Br
Molecular Weight 171.034
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of P-BROMOTOLUENE

SMILES

CC1=CC=C(Br)C=C1

InChI

InChIKey=ZBTMRBYMKUEVEU-UHFFFAOYSA-N
InChI=1S/C7H7Br/c1-6-2-4-7(8)5-3-6/h2-5H,1H3

HIDE SMILES / InChI

Molecular Formula C7H7Br
Molecular Weight 171.034
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Rate enhancement of an interfacial biochemical reaction through localization of substrate and enzyme by an adaptor domain.
2010-11-25
Cavity-shaped ligands: calix[4]arene-based monophosphanes for fast Suzuki-Miyaura cross-coupling.
2010-08-09
Arrested catalysis: controlling Kumada coupling activity via a redox-active N-heterocyclic carbene.
2010-07-14
Thermal degradation behavior of waste video cards using thermogravimetric analysis and pyrolysis gas chromatography/mass spectrometry techniques.
2010-05
Fluorogenic derivatization of aryl halides based on the formation of biphenyl by Suzuki coupling reaction with phenylboronic acid.
2009-10-02
Synthesis of 1,5-benzothiazepine dipeptide mimetics via two CuI-catalyzed cross coupling reactions.
2009-07-02
4-[(E)-4-Bromo-benzyl-ideneamino]-3-[1-(4-isobutyl-phen-yl)eth-yl]-1H-1,2,4-triazole-5(4H)-thione.
2009-05-20
Formation and crystallographic elucidation of stable [4 + 2]-coordinate nickel(II) N,S-heterocyclic carbene (NSHC) complexes.
2009-03-14
Phosphine-free, palladium-catalyzed arylation of heterocycles through C-H bond activation with pivalic acid as a cocatalyst.
2009
In vitro metabolism of a model cyclopropylamine to reactive intermediate: insights into trovafloxacin-induced hepatotoxicity.
2008-03
Palladium-catalyzed aminations of aryl halides with phosphine-functionalized imidazolium ligands.
2008-02-21
Spin-orbit ab initio investigation of the photolysis of o-, m-, and p-bromotoluene.
2008-02-14
Synthesis of valsartan via decarboxylative biaryl coupling.
2007-09-14
Iron-catalyzed homocoupling of bromide compounds.
2006-08-18
Indolyl esters and amides related to indomethacin are selective COX-2 inhibitors.
2005-12-15
Inhibitory effects of the guanine moiety on Suzuki couplings of unprotected halonucleosides in aqueous media.
2005-08-05
Remarkable substituent effects on the oxidizing ability of triarylbismuth dichlorides in alcohol oxidation.
2004-12-10
Impurity profiling of methamphetamine hydrochloride drugs seized in the Philippines.
2004-08-11
Dimethylformamide as a carbon monoxide source in fast palladium-catalyzed aminocarbonylations of aryl bromides.
2002-08-23
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:14:01 GMT 2025
Edited
by admin
on Mon Mar 31 19:14:01 GMT 2025
Record UNII
9E349GQ7EU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
P-BROMOTOLUENE
Common Name English
4-BROMOTOLUENE
HSDB  
Preferred Name English
1-METHYL-4-BROMOBENZENE
Systematic Name English
BENZENE, 1-BROMO-4-METHYL-
Systematic Name English
4-TOLYL BROMIDE
Systematic Name English
4-METHYLPHENYL BROMIDE
Systematic Name English
4-BROMOTOLUENE [HSDB]
Common Name English
4-BROMO-1-METHYLBENZENE
Systematic Name English
NSC-6531
Code English
Code System Code Type Description
EPA CompTox
DTXSID7024661
Created by admin on Mon Mar 31 19:14:01 GMT 2025 , Edited by admin on Mon Mar 31 19:14:01 GMT 2025
PRIMARY
FDA UNII
9E349GQ7EU
Created by admin on Mon Mar 31 19:14:01 GMT 2025 , Edited by admin on Mon Mar 31 19:14:01 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-391-8
Created by admin on Mon Mar 31 19:14:01 GMT 2025 , Edited by admin on Mon Mar 31 19:14:01 GMT 2025
PRIMARY
NSC
6531
Created by admin on Mon Mar 31 19:14:01 GMT 2025 , Edited by admin on Mon Mar 31 19:14:01 GMT 2025
PRIMARY
HSDB
6015
Created by admin on Mon Mar 31 19:14:01 GMT 2025 , Edited by admin on Mon Mar 31 19:14:01 GMT 2025
PRIMARY
PUBCHEM
7805
Created by admin on Mon Mar 31 19:14:01 GMT 2025 , Edited by admin on Mon Mar 31 19:14:01 GMT 2025
PRIMARY
CAS
106-38-7
Created by admin on Mon Mar 31 19:14:01 GMT 2025 , Edited by admin on Mon Mar 31 19:14:01 GMT 2025
PRIMARY