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About This Item
经验公式（希尔记法）:
C12H11Br
CAS号:
分子量:
235.12
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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质量水平
方案
97%
折射率
n20/D 1.638 (lit.)
沸点
237-238 °C/760 mmHg (lit.)
密度
1.646 g/mL at 25 °C (lit.)
官能团
bromo
SMILES字符串
BrCCc1cccc2ccccc12
InChI
1S/C12H11Br/c13-9-8-11-6-3-5-10-4-1-2-7-12(10)11/h1-7H,8-9H2
InChI key
GPHCPUFIWQJZOI-UHFFFAOYSA-N
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一般描述
1-(2-Bromoethyl)naphthalene can be obtained from the reaction between 1-(2-hydroxyethyl)naphthalene and phosphorus tribromide.
应用
1-(2-Bromoethyl)naphthalene may be used to synthesize 2-iodo-1-[2-(1-naphthyl)ethyl]-1H-benzimidazole.
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
230.0 °F - closed cup
闪点(°C)
110 °C - closed cup
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Potentially carcinogenic cyclopenta [a] phenanthrenes. Part IV. Synthesis of 17-ketones by the Stobbe condensation.
Coombs MM, et al.
J. Chem. Soc. Sect. C, 9, 1266-1271 (1970)
Access to aromatic ring-fused benzimidazoles using photochemical substitutions of the benzimidazol-2-yl radical.
O'Connell JM, et al.
Synthesis, 44(12), 3371-3377 (2012)
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