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Merck
CN

246328

Sigma-Aldrich

6-甲基吲哚

97%

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About This Item

经验公式(希尔记法):
C9H9N
CAS号:
分子量:
131.17
Beilstein:
109708
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

97%

形式

solid

折射率

n20/D 1.607 (lit.)

bp

112 °C/5 mmHg (lit.)

密度

1.059 g/mL at 25 °C (lit.)

SMILES字符串

Cc1ccc2cc[nH]c2c1

InChI

1S/C9H9N/c1-7-2-3-8-4-5-10-9(8)6-7/h2-6,10H,1H3

InChI key

ONYNOPPOVKYGRS-UHFFFAOYSA-N

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应用

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

象形图

Exclamation mark

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

WGK

WGK 3

闪点(°F)

closed cup

闪点(°C)

closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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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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