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ChemicalBook--->CAS DataBase List--->32795-84-9

32795-84-9

32795-84-9 Structure

32795-84-9 Structure
IdentificationBack Directory
[Name]

7-BROMOBENZ[A]ANTHRACENE
[CAS]

32795-84-9
[Synonyms]

Bromobenzanthracene
7-bromobenzanthracene
7-BROMOBENZ[A]ANTHRACENE
7-bromo-benz(a)anthracen
10-brom-1,2-benzanthracen
10-bromo-1,2-benzanthracene
7-BROMO-BENZ[A]ANTHRACENE 98+%
AR-E 4 7-BROMOBENZ(A)ANTHRACENE
7-Bromobenz[a]anthracene
[Molecular Formula]

C18H11Br
[MDL Number]

MFCD00029016
[MOL File]

32795-84-9.mol
[Molecular Weight]

307.18
Chemical PropertiesBack Directory
[Melting point ]

152 °C
[Boiling point ]

361.79°C (rough estimate)
[density ]

1.3995 (rough estimate)
[refractive index ]

1.6000 (estimate)
[storage temp. ]

Room Temperature, under inert atmosphere
[solubility ]

Chloroform (Slightly), Dichloromethane (Slightly)
[form ]

Solid
[color ]

Light Beige to Dark Yellow
[InChI]

InChI=1S/C18H11Br/c19-18-15-8-4-2-6-13(15)11-17-14-7-3-1-5-12(14)9-10-16(17)18/h1-11H
[InChIKey]

LGRNWCDRODWMOH-UHFFFAOYSA-N
[SMILES]

C12=CC=CC=C1C=CC1C2=CC2C(=CC=CC=2)C=1Br
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H413-H302
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P270-P301+P312-P330-P501
[RTECS ]

CW0180000
[HS Code ]

2903.99.8001
Spectrum DetailBack Directory
[Spectrum Detail]

7-BROMOBENZ[A]ANTHRACENE(32795-84-9)MS
Hazard InformationBack Directory
[Toxicity evaluation]

The tumorigenicity of 7-chlorobenz[α]anthracene (7-C1-BA), an environmental contaminant, and 7-bromobenz[α]anthracene (7-Br-BA) was determined in the male B6C3F1 newborn mouse. Mice receiving 7-C1-BA and 7-Br-BA by i.p. injections at a dose of 1600 nmol per mouse on 1, 8, and 15 days after birth developed 92 and 96% hepatocellular adenomas, and 100 and 83% hepatocellular carcinoma, respectively. Metabolism by liver microsomes of 15-day-old mice each produced the corresponding trans-3,4-dihydrodiol. Analysis by 32P-postlabeling/HPLC indicated the presence of DNA adducts derived from 7-C1-BA trans-3,4-dihydrodiol and 7-Br-BA trans-3,4-dihydrodiol. The results indicate that both 7-C1-BA and 7-Br-BA are potent carcinogens and that bay-region diol epoxides are the ultimate metabolites that lead to DNA adduct formation and tumor initiation[1].
[References]

[1] Peter P. Fu. “Potent tumorigenicity of 7-chlorobenz[α]anthracene and 7-bromobenz[α]anthracene in the neonatal B6C3F1 male mouse.” Cancer letters 101 1 (1996): Pages 37-42.
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