246328
6-甲基吲哚
97%
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关于此项目
经验公式（希尔记法）:
C9H9N
化学文摘社编号:
分子量:
131.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
109708
Assay:
97%
Form:
solid
InChI
1S/C9H9N/c1-7-2-3-8-4-5-10-9(8)6-7/h2-6,10H,1H3
SMILES string
Cc1ccc2cc[nH]c2c1
InChI key
ONYNOPPOVKYGRS-UHFFFAOYSA-N
assay
97%
form
solid
refractive index
n20/D 1.607 (lit.)
bp
112 °C/5 mmHg (lit.)
density
1.059 g/mL at 25 °C (lit.)
Quality Level
Application
6-Methylindole was used in the synthesis of benz[c,d]indol-3(1H)-one derivatives.
- Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators
- Reactant for preparation of indole linked triazole derivatives as antifungal agents
- Reactant for preparation of N-β-D-xylosyl-indole derivatives as SGLT2 inhibitors for management of hyperglycemia in diabetes
- Reactant for preparation of aminoguanidine derivatives of arylsulfonylacylindoles as antifungal agents
- Reactant for preparation of indolylindazoles and indolylpyrazolopyridines as interleukin-2 inducible T cell kinase inhibitors
- Reactant for preparation of arylsulfonylacetylindoles as anti-HIV-1 agents
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Taichi Komoda et al.
Bioscience, biotechnology, and biochemistry, 67(3), 659-662 (2003-05-02)
The new inhibitors of 3alpha-hydroxysteroid dehydrogenase, 0231A 1 and 0231B 2, have a unique benz[c,d]indol-3(1H)-one structure in their molecules. In our advanced studies on indole chemistry, we have developed an efficient synthetic method for benz[c,d]indol-3(1H)-one derivatives. We report here its
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