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Details

Stereochemistry ACHIRAL
Molecular Formula C7H7BrO
Molecular Weight 187.034
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-Bromoanisole

SMILES

COC1=CC=C(Br)C=C1

InChI

InChIKey=QJPJQTDYNZXKQF-UHFFFAOYSA-N
InChI=1S/C7H7BrO/c1-9-7-4-2-6(8)3-5-7/h2-5H,1H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis and X-ray structure determination of highly active Pd(II), Pd(I), and Pd(0) complexes of di(tert-butyl)neopentylphosphine (DTBNpP) in the arylation of amines and ketones.
2010-10-01
4-(4-Meth-oxy-phen-yl)-2-methyl-but-3-yn-2-ol.
2010-06-30
Palladium complexes with a tridentate PNO ligand. Synthesis of eta1-allyl complexes and cross-coupling reactions promoted by boron compounds.
2010-04-21
The endocytic recycling regulator EHD1 is essential for spermatogenesis and male fertility in mice.
2010-04-02
3-(3-Bromo-4-methoxy-phen-yl)-1,5-diphenyl-pentane-1,5-dione.
2010-03-13
Fluorogenic derivatization of aryl halides based on the formation of biphenyl by Suzuki coupling reaction with phenylboronic acid.
2009-10-02
N-heterocycle carbene (NHC)-ligated cyclopalladated N,N-dimethylbenzylamine: a highly active, practical and versatile catalyst for the Heck-Mizoroki reaction.
2009-05-21
Formation and crystallographic elucidation of stable [4 + 2]-coordinate nickel(II) N,S-heterocyclic carbene (NSHC) complexes.
2009-03-14
(E)-N'-(5-Bromo-2-methoxy-benzyl-idene)-4-methoxy-benzohydrazide.
2008-11-08
Methanolysis of 4-bromobenzenediazonium ions. Effects of acidity, [MeOH] and temperature on the formation and decomposition of diazo ethers that initiate homolytic dediazoniation.
2008-11-07
The Wurtz-Fittig reaction in the preparation of C-silylated calixarenes.
2007-10-12
Isolation and characterisation of impurities in adapalene.
2007-02-19
Orientational isomerism and binding ability of nonsymmetrical guests encapsulated in a self-assembling heterodimeric capsule.
2005-08-05
Fluorescence labeling method for aryl halides with 4-(4,5-diphenyl-1H-imidazol-2-yl)phenylboronic acid based on Suzuki coupling reaction.
2005-02-25
Inclusion compounds of tetrakis(4-nitrophenyl)methane: C-H...O networks, pseudopolymorphism, and structural transformations.
2001-05-16
Patents
Name Type Language
NSC-8042
Preferred Name English
4-Bromoanisole
Systematic Name English
4-ANISYL BROMIDE
Systematic Name English
P-BROMOMETHOXYBENZENE
Common Name English
4-BROMOANISOL
Systematic Name English
4-BROMOMETHOXYBENZENE
Systematic Name English
4-METHOXY-1-BROMOBENZENE
Systematic Name English
1-Bromo-4-methoxybenzene
Systematic Name English
1-METHOXY-4-BROMOBENZENE
Systematic Name English
BROMOPHENOL P-FORM METHYL ETHER [MI]
Common Name English
4-METHOXYPHENYL BROMIDE
Systematic Name English
P-BROMANISOLE
Common Name English
P-ANISYL BROMIDE
Common Name English
4-METHOXYBROMOBENZENE
Systematic Name English
ANISOLE, P-BROMO-
Common Name English
P-BROMOANISOLE
Common Name English
4-BROMO-1-METHOXYBENZENE
Systematic Name English
Code System Code Type Description
CHEBI
47257
Created by admin on Mon Mar 31 21:22:39 GMT 2025 , Edited by admin on Mon Mar 31 21:22:39 GMT 2025
PRIMARY
PUBCHEM
7730
Created by admin on Mon Mar 31 21:22:39 GMT 2025 , Edited by admin on Mon Mar 31 21:22:39 GMT 2025
PRIMARY
FDA UNII
U430F901J9
Created by admin on Mon Mar 31 21:22:39 GMT 2025 , Edited by admin on Mon Mar 31 21:22:39 GMT 2025
PRIMARY
MERCK INDEX
m2709
Created by admin on Mon Mar 31 21:22:39 GMT 2025 , Edited by admin on Mon Mar 31 21:22:39 GMT 2025
PRIMARY Merck Index
CAS
104-92-7
Created by admin on Mon Mar 31 21:22:39 GMT 2025 , Edited by admin on Mon Mar 31 21:22:39 GMT 2025
PRIMARY
NSC
8042
Created by admin on Mon Mar 31 21:22:39 GMT 2025 , Edited by admin on Mon Mar 31 21:22:39 GMT 2025
PRIMARY
WIKIPEDIA
4-Bromoanisole
Created by admin on Mon Mar 31 21:22:39 GMT 2025 , Edited by admin on Mon Mar 31 21:22:39 GMT 2025
PRIMARY
EPA CompTox
DTXSID2059308
Created by admin on Mon Mar 31 21:22:39 GMT 2025 , Edited by admin on Mon Mar 31 21:22:39 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-252-1
Created by admin on Mon Mar 31 21:22:39 GMT 2025 , Edited by admin on Mon Mar 31 21:22:39 GMT 2025
PRIMARY