684910
1H-苯并[g]吲哚
97%
别名:
1H-Benz[g]indole, 6,7-苯并吲哚, NSC 153687
登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式（希尔记法）:
C12H9N
化学文摘社编号:
分子量:
167.21
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
solid
产品名称
1H-苯并[g]吲哚, 97%
InChI
1S/C12H9N/c1-2-4-11-9(3-1)5-6-10-7-8-13-12(10)11/h1-8,13H
SMILES string
c1ccc2c(c1)ccc3cc[nH]c23
InChI key
HIYWOHBEPVGIQN-UHFFFAOYSA-N
assay
97%
form
solid
mp
180-184 °C
Quality Level
Application
- 作为反应物，用于制备色氨酸双加氧酶抑制剂吡啶基-乙烯基-吲哚——一种潜在的抗癌免疫调节剂
可用作吲哚化学反应中起始物质的稠合吲哚。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Dam. 1
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Jason Siu et al.
Organic & biomolecular chemistry, 2(2), 160-167 (2004-01-23)
The development of enhanced conditions for Lewis acid catalysed Leimgruber-Batcho indole synthesis using microwave acceleration is described. This approach has permitted the preparation of a variety of heteroaromatic enamine intermediates in good yield and high purities. Subsequent catalytic hydrogenation reactions
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持