质量水平
方案
98%
表单
solid
mp
>300 °C (lit.)
溶解性
chloroform: soluble 10 mg/mL
官能团
bromo
SMILES字符串
Brc1c(Br)c(Br)c(Br)c(Br)c1Br
InChI
1S/C6Br6/c7-1-2(8)4(10)6(12)5(11)3(1)9
InChI key
CAYGQBVSOZLICD-UHFFFAOYSA-N
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一般描述
Hexabromobenzene is used as fire retardant in plastics, paper and electric manufactured goods. It undergoes protodebromination when treated with sodium methoxide in methanol and ethyl methyl ketone to give a mixture of tetrabromobenzenes.
应用
The porphyrinogenic potential of hexabromobenzene (HBB) with hexachlorobenzene was studied in the liver of primiparous rats.
警示用语:
Warning
危险分类
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 4 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Comparison of the porphyrinogenic activity of hexabromobenzene and hexachlorobenzene in primiparous Wistar rats.
C E Mendoza et al.
Bulletin of environmental contamination and toxicology, 21(3), 358-364 (1979-02-01)
Polyhalogeno-aromatic compounds. Part VIII. Reactions of hexabromobenzene with nucleophiles.
Collins I and Suschitzky H.
J. Chem. Soc. Sect. C, 18, 2337-2341 (1969)
Uptake of chloro- and bromobiphenyls, hexachloro- and hexabromobenzene by fish.
V Zitko et al.
Bulletin of environmental contamination and toxicology, 16(6), 665-673 (1976-12-01)
Hans Peter H Arp et al.
Journal of environmental monitoring : JEM, 13(3), 505-513 (2010-12-09)
The brominated flame retardants (BFRs), pentabromotoluene (PBT), pentabromoethylbenzene (PBEB) and hexabromobenzene (HBB), exhibit physical-chemical properties similar to other persistent organic pollutants, and have been in use as flame retardants for several decades. Data on these BFRs in diverse environmental samples
Joanna Wencel-Delord et al.
Angewandte Chemie (International ed. in English), 51(52), 13001-13005 (2012-10-23)
C(6)Br(six) & drugs! C(6)Br(6) can be used as the cooxidant/catalyst modifier for the [Rh(III)Cp*]-catalyzed (Cp*=C(5)Me(5)) dehydrogenative cross-coupling of benzamides with simple benzene derivatives (see scheme, DG=directing group). Similarly, heterocycles can be coupled and druglike structures formed. Mechanistic studies suggest a
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