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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 O-DIBROMOBENZENE

SMILES

BrC1=CC=CC=C1Br

InChI

InChIKey=WQONPSCCEXUXTQ-UHFFFAOYSA-N
InChI=1S/C6H4Br2/c7-5-3-1-2-4-6(5)8/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
Enantiopure 1,2-bis(tert-butylmethylphosphino)benzene as a highly efficient ligand in rhodium-catalyzed asymmetric hydrogenation.
2010-10-01
1,2-Bis(2-methyl-5-phenyl-3-thien-yl)benzene.
2009-11-07
Modular synthesis of indoles from imines and o-dihaloarenes or o-chlorosulfonates by a Pd-catalyzed cascade process.
2009-03-25
Development of an enzyme-linked immunosorbent assay for determination of the miticide bromopropylate.
2009-01-28
A novel modular approach to triazole-functionalized phthalocyanines using click chemistry.
2009-01-02
Static and dynamic bimolecular fluorescence quenching of porphyrin dendrimers in solution.
2008-09
Bulky N-substituted 1,3-benzazaphospholes: access via Pd-catalyzed C-N and C-P cross coupling, lithiation, and conversion to novel P=C-PtBu2 hybrid ligands.
2008-08-04
Copper-catalyzed domino annulation approaches to the synthesis of benzoxazoles under microwave-accelerated and conventional thermal conditions.
2008-05-02
Household vacuum cleaners vs. the high-volume surface sampler for collection of carpet dust samples in epidemiologic studies of children.
2008-02-21
Halogen-metal exchange in 1,2-dibromobenzene and the possible intermediacy of 1,2-dilithiobenzene.
2007-12-07
Integrated micro flow synthesis based on sequential Br-Li exchange reactions of p-, m-, and o-dibromobenzenes.
2007-12-03
Reaction of 1,2-dibromobenzene with the Si(111)-7x7 surface, a DFT study.
2005-12-08
An advantageous route to oxcarbazepine (trileptal) based on palladium-catalyzed arylations free of transmetallating agents.
2005-10-27
Synthesis and optical resolution of 9,9'-spirobifluorene-1,1'-diol.
2004-07-08
Regiospecific metalation of oligobromobenzenes.
2003-06-27
Analytical procedure for the determination of chlorobenzenes in sediments.
2003-02
Comparison of tissue distribution and metabolism of 1,2- and 1,4-dibromobenzenes in female rats.
2002
Hepatotoxicity of brominated benzenes: relationship between chemical structure and hepatotoxic effects in acute intoxication of mice.
1998
Comparison of hepatotoxicity of 1,2-, 1,3- and 1,4-dibromobenzenes: the dynamics of changes of selected parameters of liver necrosis in acute poisoning in mice.
1996-01-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:07:41 GMT 2025
Edited
by admin
on Mon Mar 31 22:07:41 GMT 2025
Record UNII
52K9W7U6EH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
O-DIBROMOBENZENE
Common Name English
NSC-60643
Preferred Name English
1,2-DIBROMOBENZENE
Systematic Name English
BENZENE, O-DIBROMO-
Common Name English
BENZENE, 1,2-DIBROMO-
Systematic Name English
Code System Code Type Description
WIKIPEDIA
1,2-Dibromobenzene
Created by admin on Mon Mar 31 22:07:41 GMT 2025 , Edited by admin on Mon Mar 31 22:07:41 GMT 2025
PRIMARY
NSC
60643
Created by admin on Mon Mar 31 22:07:41 GMT 2025 , Edited by admin on Mon Mar 31 22:07:41 GMT 2025
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EPA CompTox
DTXSID0022064
Created by admin on Mon Mar 31 22:07:41 GMT 2025 , Edited by admin on Mon Mar 31 22:07:41 GMT 2025
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ECHA (EC/EINECS)
209-507-3
Created by admin on Mon Mar 31 22:07:41 GMT 2025 , Edited by admin on Mon Mar 31 22:07:41 GMT 2025
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CAS
583-53-9
Created by admin on Mon Mar 31 22:07:41 GMT 2025 , Edited by admin on Mon Mar 31 22:07:41 GMT 2025
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CHEBI
37152
Created by admin on Mon Mar 31 22:07:41 GMT 2025 , Edited by admin on Mon Mar 31 22:07:41 GMT 2025
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FDA UNII
52K9W7U6EH
Created by admin on Mon Mar 31 22:07:41 GMT 2025 , Edited by admin on Mon Mar 31 22:07:41 GMT 2025
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PUBCHEM
11414
Created by admin on Mon Mar 31 22:07:41 GMT 2025 , Edited by admin on Mon Mar 31 22:07:41 GMT 2025
PRIMARY