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
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
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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