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质量水平
方案
97%
mp
97-99 °C (lit.)
溶解性
chloroform: soluble 25 mg/mL, clear, yellow
官能团
bromo
SMILES字符串
BrCCc1c[nH]c2ccccc12
InChI
1S/C10H10BrN/c11-6-5-8-7-12-10-4-2-1-3-9(8)10/h1-4,7,12H,5-6H2
InChI key
NTLAICDKHHQUGC-UHFFFAOYSA-N
一般描述
3-(2-Bromoethyl)indole is a halogenated heterocyclic building block.
应用
3-(2-Bromoethyl)indole may be used in the synthesis of:
- β-carboline derivatives
- 6,7-dihydro-12H-indolo[2,3-a] pyridocolinium bromide
- N-(2-(3-indolyl)ethyl)aza-12-crown-4
- N-(2-(3-Indolyl)ethyl)aza-15-crown-5
- N-(2-(3-Indolyl)ethyl)aza-18-crown-6
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
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
从最新的版本中选择一种：
分析证书(COA)
Lot/Batch Number
Jiaxin Hu et al.
Proceedings of the National Academy of Sciences of the United States of America, 99(8), 5121-5126 (2002-04-12)
Feeble forces play a significant role in the organization of proteins. These include hydrogen bonding, hydrophobic interactions, salt bridge formation, and steric interactions. The alkali metal cation-pi interaction is a force of potentially profound importance but its consideration in biology
The synthesis of ?-carboline derivatives-I: A synthesis of some 12 H-indolo [2, 3-a] pyridocolinium salts, including flavopereirine.
Ban Y and Seo M.
Tetrahedron, 16(1), 5-10 (1961)
The synthesis of beta-carboline derivatives. VII. The isolation of the possible intermediate in the condensation of 3-(2-bromoethyl)indole and 2-halogenopyridine.
Y Ban et al.
Chemical & pharmaceutical bulletin, 13(8), 931-934 (1965-08-01)
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