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Details

Stereochemistry MIXED
Molecular Formula C8H12Br4
Molecular Weight 427.797
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-(1,2-DIBROMOETHYL)-3,4-DIBROMOCYCLOHEXANE

SMILES

BrCC(Br)C1CCC(Br)C(Br)C1

InChI

InChIKey=PQRRSJBLKOPVJV-UHFFFAOYSA-N
InChI=1S/C8H12Br4/c9-4-8(12)5-1-2-6(10)7(11)3-5/h5-8H,1-4H2

HIDE SMILES / InChI

Molecular Formula C8H12Br4
Molecular Weight 427.797
Charge 0
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
1,2-Dibromo-4-(1,2-dibromoethyl)-cyclohexane and tris(methylphenyl) phosphate cause significant effects on development, mRNA expression, and circulating bile acid concentrations in chicken embryos.
2014-06-15
1,2-Dibromo-4-(1,2 dibromoethyl) cyclohexane (TBECH)-mediated steroid hormone receptor activation and gene regulation in chicken LMH cells.
2014-04
Use of an avian hepatocyte assay and the avian Toxchip Polymerse chain reaction array for testing prioritization of 16 organic flame retardants.
2014-03
The brominated flame retardant TBECH activates the zebrafish (Danio rerio) androgen receptor, alters gene transcription and causes developmental disturbances.
2013-10-15
Accumulation of polybrominated diphenyl ethers, hexabromobenzene, and 1,2-dibromo-4-(1,2-dibromoethyl)cyclohexane in earthworm (Eisenia fetida). Effects of soil type and aging.
2010-12-01
Brominated flame retardants in the Arctic environment--trends and new candidates.
2010-07-01
Biodegradation kinetics of selected brominated flame retardants in aerobic and anaerobic soil.
2010-06
Diastereomers of the brominated flame retardant 1,2-dibromo-4-(1,2 dibromoethyl)cyclohexane induce androgen receptor activation in the hepg2 hepatocellular carcinoma cell line and the lncap prostate cancer cell line.
2009-12
Uptake and biotransformation of structurally diverse brominated flame retardants in zebrafish (Danio rerio) after dietary exposure.
2009-05
Temporal trends and spatial distribution of non-polybrominated diphenyl ether flame retardants in the eggs of colonial populations of Great Lakes herring gulls.
2009-01-15
In vitro biologic activities of the antimicrobials triclocarban, its analogs, and triclosan in bioassay screens: receptor-based bioassay screens.
2008-09
Structure characterization and thermal stabilities of the isomers of the brominated flame retardant 1,2-dibromo-4-(1,2-dibromoethyl)cyclohexane.
2008-07
Identilication of the novel cycloaliphatic brominated flame retardant 1,2-dibromo-4-(1,2-dibromoethyl)cyclohexane in Canadian Arctic beluga (Delphinapterus leucas).
2008-01-15
Identification of the brominated flame retardant 1,2-dibromo-4-(1,2-dibromoethyl)cyclohexane as an androgen agonist.
2006-12-14
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:22:53 GMT 2025
Edited
by admin
on Mon Mar 31 22:22:53 GMT 2025
Record UNII
502D5Q149T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CITEX BCL 462
Preferred Name English
1-(1,2-DIBROMOETHYL)-3,4-DIBROMOCYCLOHEXANE
HSDB  
Systematic Name English
CYCLOHEXANE, 1,2-DIBROMO-4-(1,2-DIBROMOETHYL)-
Systematic Name English
SAYTEX BCL 462
Brand Name English
4-(1,2-DIBROMOETHYL)-1,2-DIBROMOCYCLOHEXANE
Systematic Name English
1,2-DIBROMO-4-(1,2-DIBROMOETHYL)CYCLOHEXANE
Systematic Name English
VINYLCYCLOHEXENE TETRABROMIDE
Systematic Name English
1-(1,2-DIBROMOETHYL)-3,4-DIBROMOCYCLOHEXANE [HSDB]
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
222-036-8
Created by admin on Mon Mar 31 22:22:53 GMT 2025 , Edited by admin on Mon Mar 31 22:22:53 GMT 2025
PRIMARY
CAS
3322-93-8
Created by admin on Mon Mar 31 22:22:53 GMT 2025 , Edited by admin on Mon Mar 31 22:22:53 GMT 2025
PRIMARY
PUBCHEM
18728
Created by admin on Mon Mar 31 22:22:53 GMT 2025 , Edited by admin on Mon Mar 31 22:22:53 GMT 2025
PRIMARY
EPA CompTox
DTXSID8024947
Created by admin on Mon Mar 31 22:22:53 GMT 2025 , Edited by admin on Mon Mar 31 22:22:53 GMT 2025
PRIMARY
HSDB
6146
Created by admin on Mon Mar 31 22:22:53 GMT 2025 , Edited by admin on Mon Mar 31 22:22:53 GMT 2025
PRIMARY
FDA UNII
502D5Q149T
Created by admin on Mon Mar 31 22:22:53 GMT 2025 , Edited by admin on Mon Mar 31 22:22:53 GMT 2025
PRIMARY