1402730-50-0

Basic information

• Product Name: (rac)-2-phenyl-1,2-dihydro-1'H-[2,3']biindolyl-3-one
• Synonyms: (rac)-2-phenyl-1,2-dihydro-1'H-[2,3']biindolyl-3-one
• CAS NO: 1402730-50-0
• Molecular Weight: 324.382
• Mol File: 1402730-50-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (rac)-2-phenyl-1,2-dihydro-1'H-[2,3']biindolyl-3-one(CAS DataBase Reference)
• NIST Chemistry Reference: (rac)-2-phenyl-1,2-dihydro-1'H-[2,3']biindolyl-3-one(1402730-50-0)
• EPA Substance Registry System: (rac)-2-phenyl-1,2-dihydro-1'H-[2,3']biindolyl-3-one(1402730-50-0)

Safety Data

• Hazardous Substances Data: 1402730-50-0(Hazardous Substances Data)

Upstream product

• 120-72-9 indole 
• 948-65-2 2-phenyl-indole 
• 2989-63-1 2-phenyl-3H-indol-3-one 
• 1969-74-0 2-phenylisatogen 

Relevant articles and documents

Oxidative dearomative cross-dehydrogenative coupling of indoles with diverse C-H nucleophiles: Efficient Approach to 2,2-Disubstituted Indolin-3-ones

The oxidative, dearomative cross-dehydrogenative coupling of indoles with various C-H nucleophiles is developed. This process features a broad substrate scope with respect to both indoles and nucleophiles, affording structurally diverse 2,2-disubstituted indolin-3-ones in high yields (up to 99%). The oxidative dimerization and trimerization of indoles has also been demonstrated under the same conditions.

Indolyl substituted indole-3-ketone and synthesis method thereof

The invention relates to an indolyl substituted indole-3-ketone and a synthesis method thereof. According to the method, an indole compound and an o-nitro alkyne compound are converted into the indolyl substituted indole-3-ketone in the argon atmosphere under a PPh3 reducing agent for the first time, and the prepared indole substituted indole-3-ketone is stable in molecular structure and excellentin chemical property. Reaction raw materials of the synthesis method are cheap and easy to obtain, and pretreatment is not needed; only acid and a reducing agent are used in the reaction without a metal catalyst so that raw materials are saved and the reaction cost is reduced; the whole reaction system is simple, reaction conditions are mild, reaction equipment is less, experimental operation issimple and convenient, and material sources are wide.