116388-35-3

Basic information

• Product Name: 1H-Indole, 1,2,5,6-tetramethyl-
• CAS NO: 116388-35-3
• Molecular Formula: C12H15N
• Molecular Weight: 173.258
• Mol File: 116388-35-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1H-Indole, 1,2,5,6-tetramethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole, 1,2,5,6-tetramethyl-(116388-35-3)
• EPA Substance Registry System: 1H-Indole, 1,2,5,6-tetramethyl-(116388-35-3)

Safety Data

• Hazardous Substances Data: 116388-35-3(Hazardous Substances Data)

Upstream product

• 6407-34-7 methyl-1 ethylideneamine 
• 95-64-7 4-amino-o-xylene 
• 67-64-1 acetone 
• 110-89-4 piperidine 

Relevant articles and documents

Cu-Catalyzed Oxidation of C2 and C3 Alkyl-Substituted Indole via Acyl Nitroso Reagents

The selective oxidation of C2-alkyl-substituted indoles to 3-oxindole and the selective C-H oxygenation or amination of C2,C3-dialkyl-substituted indoles at C2 are reported under mild conditions. The position of the alkyl substitution on the indole directs the reaction to different pathways under similar conditions.

SYNTHESIS OF INDOLES FROM PYRIDINIUM SALTS. 4. KETIMINES IN THE SYNTHESIS OF INDOLES FROM 3-NITROPYRIDINIUM SALTS

The possibility of using certain ketimines in place of mixtures of ketone and amine in the synthesis of indoles from 3-nitropyridinium salts has been demonstrated.The use of ketimines leads, in many cases, to increased yields of indoles and simplifies their isolation.It has been established that the rate of indole formation is considerably increased in polar aprotic solvents.