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蒸汽密度
5.41 (vs air)
质量水平
蒸汽压
10 mmHg ( 40 °C)
方案
≥99.5% (GC)
表单
liquid
自燃温度
1051 °F
expl. lim.
36.5 %
折射率
n20/D 1.559 (lit.)
n20/D 1.559
沸点
156 °C (lit.)
mp
−31 °C (lit.)
溶解性
alcohol: soluble 10.4g/100g at 25 °C
diethyl ether: soluble 71.3g/100g at 25 °C
water: insoluble 0.045g/100g at 30 °C (practically)
benzene: miscible
chloroform: miscible
hydrocarbons: miscible (petr.)
密度
1.491 g/mL at 25 °C (lit.)
官能团
bromo
SMILES字符串
Brc1ccccc1
InChI
1S/C6H5Br/c7-6-4-2-1-3-5-6/h1-5H
InChI key
QARVLSVVCXYDNA-UHFFFAOYSA-N
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应用
溴苯被用于合成制备两亲性星形接枝共聚物所需的四臂星形链转移剂 。
生化/生理作用
溴苯通过形成反应性代谢产物芳香化重要的细胞大分子，诱导肝坏死 。
警示用语：
Warning
危险声明
危险分类
Aquatic Chronic 2 - Flam. Liq. 3 - Skin Irrit. 2
储存分类代码
3 - Flammable liquids
WGK
WGK 2
闪点(°F)
123.8 °F - closed cup
闪点(°C)
51.0 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
Star-like PAA-g-PPO well-defined amphiphilic graft copolymer synthesized by ATNRC and SET-NRC reaction.
Li Y, et al.
Journal of Polymer Science: Part A, General Papers, 48(10), 2084-2097 (2010)
Bromobenzene-induced liver necrosis. Protective role of glutathione and evidence for 3,4-bromobenzene oxide as the hepatotoxic metabolite.
D J Jollow et al.
Pharmacology, 11(3), 151-169 (1974-01-01)
Yuning Ma et al.
Environmental science & technology, 46(24), 13112-13117 (2012-11-28)
The 2,4,6-tribromophenoxy moiety is a common structural feature of several brominated flame retardants, and we have previously reported on the environmental concentrations of one such compound, 1,2-bis(2,4,6-tribromophenoxy) ethane (TBE). Here we report the atmospheric concentrations of TBE and three other
Hiroyuki Asakura et al.
The journal of physical chemistry. A, 116(16), 4029-4034 (2012-04-14)
A homocoupling reaction mechanism of bromobenzene mediated by the [Ni(cod)(bpy)] (cod = 1,5-cyclooctadiene; bpy = 2,2'-bipyridine) complex was investigated by means of in situ time-resolved X-ray absorption fine structure (XAFS) and factor analysis. A dimer intermediate [Ni(bpy)(Ph)Br](2) proposed in the
Lukas Werner et al.
The Journal of organic chemistry, 76(24), 10050-10067 (2011-10-20)
Four generations of chemoenzymatic approaches to oseltamivir are presented. The first two generations relied on the use of cyclohexadiene-cis-diol derived enzymatically from bromobenzene. The third and fourth generation used the corresponding diol obtained from ethyl benzoate by fermentation with E.
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