所有图片(1)
About This Item
经验公式（希尔记法）:
C10H11FN2 · HCl
CAS号:
分子量:
214.67
EC 号:
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
99%
表单
powder
mp
233-235 °C (lit.)
SMILES字符串
Cl.NCCc1c[nH]c2cc(F)ccc12
InChI
1S/C10H11FN2.ClH/c11-8-1-2-9-7(3-4-12)6-13-10(9)5-8;/h1-2,5-6,13H,3-4,12H2;1H
InChI key
ODVDIBHWTMTHOS-UHFFFAOYSA-N
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应用
Reactant for preparation of:
- Indole alkaloid drug candidates
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
法规信息
新产品
Demosthenes Fokas et al.
Molecular diversity, 9(1-3), 81-89 (2005-03-26)
A series of diverse indole-based chemotypes were synthesized from beta-tetrahydrocarboline (beta-THC) scaffolds prepared from commercially and readily available tryptamines and alpha-ketoesters. Diversity can be generated within these chemotypes through the following strategies: (a) appendage of substituents to the beta-THC scaffold
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