U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C6H4Br2
Molecular Weight 235.904
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of P-DIBROMOBENZENE

SMILES

BrC1=CC=C(Br)C=C1

InChI

InChIKey=SWJPEBQEEAHIGZ-UHFFFAOYSA-N
InChI=1S/C6H4Br2/c7-5-1-2-6(8)4-3-5/h1-4H

HIDE SMILES / InChI

Molecular Formula C6H4Br2
Molecular Weight 235.904
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Impact of ligands on CO2 adsorption in metal-organic frameworks: first principles study of the interaction of CO2 with functionalized benzenes. I. Inductive effects on the aromatic ring.
2009-05-21
Photodissociation of dibromobenzenes at 266 nm by the velocity imaging technique.
2008-08-25
Synthesis and characterization of chiral benzylic ether-bridged periodic mesoporous organosilicas.
2008
Diethyl 2-tert-butyl-6,9-dibromo-4,11-dioxo-5,10-dihydro-cis-1H,3H,4H,11H-2-azo-3a,4a,10a,11a-tetra-aza-benz[f]indeno[2,1,7-ija]azulene-11b,11c-dicarboxyl-ate.
2007-12-06
Integrated micro flow synthesis based on sequential Br-Li exchange reactions of p-, m-, and o-dibromobenzenes.
2007-12-03
Identification, quantitation and method validation for the analysis of suspected allergens in fragrances by comprehensive two-dimensional gas chromatography coupled with quadrupole mass spectrometry and with flame ionization detection.
2007-05-25
Semi-quantitative immunohistochemical analysis of male rat-specific alpha2u-globulin accumulation for chemical toxicity evaluation.
2006-02
The effect of repeated administration of selected benzene bromoderivatives on the liver catalase activity in rats.
2005
Chemistry on a peg-board: the effect of adatom-adatom separation on the reactivity of dihalobenzenes at Si(111)7 x 7 surfaces.
2004-06-15
2,6-Diphenylbenzo[1,2-b:4,5-b']dichalcogenophenes: a new class of high-performance semiconductors for organic field-effect transistors.
2004-04-28
Photodissociation of bromobenzene, dibromobenzene, and 1,3,5-tribromobenzene.
2004-04-08
Effect of molecular oxygen on the variable-temperature 29Si MAS NMR spectra of zeolite-sorbate complexes.
2004-02-11
Guest-induced assembly of tetracarboxyl-cavitand and tetra(3-pyridyl)-cavitand into a heterodimeric capsule via hydrogen bonds and CH-halogen and/or CH-pi interaction: control of the orientation of the encapsulated guest.
2003-09-03
Comparison of tissue distribution and metabolism of 1,2- and 1,4-dibromobenzenes in female rats.
2002
Photodegradation of halobenzenes in water ice.
2001
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:29:48 GMT 2025
Edited
by admin
on Mon Mar 31 19:29:48 GMT 2025
Record UNII
9991W3M5HZ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
P-DIBROMOBENZENE
HSDB   MI  
Common Name English
NSC-33942
Preferred Name English
P-DIBROMOBENZENE [HSDB]
Common Name English
1,4-DIBROMOBENZENE
Systematic Name English
DIBROMOBENZENE, 1,4-
Systematic Name English
P-DIBROMOBENZENE [MI]
Common Name English
Code System Code Type Description
MESH
C066656
Created by admin on Mon Mar 31 19:29:48 GMT 2025 , Edited by admin on Mon Mar 31 19:29:48 GMT 2025
PRIMARY
EPA CompTox
DTXSID4024012
Created by admin on Mon Mar 31 19:29:48 GMT 2025 , Edited by admin on Mon Mar 31 19:29:48 GMT 2025
PRIMARY
CHEBI
37150
Created by admin on Mon Mar 31 19:29:48 GMT 2025 , Edited by admin on Mon Mar 31 19:29:48 GMT 2025
PRIMARY
HSDB
2734
Created by admin on Mon Mar 31 19:29:48 GMT 2025 , Edited by admin on Mon Mar 31 19:29:48 GMT 2025
PRIMARY
MERCK INDEX
m4294
Created by admin on Mon Mar 31 19:29:48 GMT 2025 , Edited by admin on Mon Mar 31 19:29:48 GMT 2025
PRIMARY Merck Index
FDA UNII
9991W3M5HZ
Created by admin on Mon Mar 31 19:29:48 GMT 2025 , Edited by admin on Mon Mar 31 19:29:48 GMT 2025
PRIMARY
WIKIPEDIA
1,4-DIBROMOBENZENE
Created by admin on Mon Mar 31 19:29:48 GMT 2025 , Edited by admin on Mon Mar 31 19:29:48 GMT 2025
PRIMARY
CAS
106-37-6
Created by admin on Mon Mar 31 19:29:48 GMT 2025 , Edited by admin on Mon Mar 31 19:29:48 GMT 2025
PRIMARY
NSC
33942
Created by admin on Mon Mar 31 19:29:48 GMT 2025 , Edited by admin on Mon Mar 31 19:29:48 GMT 2025
PRIMARY
PUBCHEM
7804
Created by admin on Mon Mar 31 19:29:48 GMT 2025 , Edited by admin on Mon Mar 31 19:29:48 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-390-2
Created by admin on Mon Mar 31 19:29:48 GMT 2025 , Edited by admin on Mon Mar 31 19:29:48 GMT 2025
PRIMARY