760213-01-2

Basic information

• Product Name: 1H-Indole-6,7-dione, 3-methyl-4-[(phenylmethyl)thio]-
• CAS NO: 760213-01-2
• Molecular Formula: C16H13NO2S
• Molecular Weight: 283.351
• Mol File: 760213-01-2.mol

Chemical Properties

• CAS DataBase Reference: 1H-Indole-6,7-dione, 3-methyl-4-[(phenylmethyl)thio]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole-6,7-dione, 3-methyl-4-[(phenylmethyl)thio]-(760213-01-2)
• EPA Substance Registry System: 1H-Indole-6,7-dione, 3-methyl-4-[(phenylmethyl)thio]-(760213-01-2)

Safety Data

• Hazardous Substances Data: 760213-01-2(Hazardous Substances Data)

Upstream product

• 760213-06-7 4-(benzylsulfanyl)-3-methyl-1-(p-tosyl)indole-6,7-dione 
• 760213-03-4 6,7-dimethoxy-3-methyl-1-(p-tosyl)indole 
• 760213-05-6 3-methyl-1-(p-tosyl)indole-6,7-dione 
• 760213-02-3 6,7-dimethoxy-3-methylindole 
• 170489-28-8 6,7-dimethoxyindole-3-carboxaldehyde 
• 100-53-8 phenylmethanethiol 
• 1025992-81-7 4-benzylsulfanyl-3-methyl-1-(toluene-4-sulfonyl)-1H-indole-6,7-diol 

Relevant articles and documents

A model compound of the novel organic cofactor CTQ (cysteine tryptophylquinone) of quinohemoprotein amine dehydrogenase

A model compound of the novel organic cofactor CTQ (cysteine tryptophylquinone) of quinohemoprotein amine dehydrogenase (QH-AmDH) has been synthesized for the first time by the Michael addition of phenylmethanethiol to the 3-methyl-6,7-indolequinone derivative as a key step. The model compound replicates the characteristic absorption spectrum of native CTQ as well as its redox potential in the subunit of QH-AmDH. Detailed structural and spectroscopic characterizations of the model compound have provided important insights into the substituent effects of the thioether group of CTQ. Wiley-VCH Verlag GmbH & Co, KGaA, 69451 Weinheim, Germany, 2004.