70691-68-8

Basic information

• Product Name: 2-methyl-3-(phenylsulfanyl)naphthoquinone
• Synonyms: 2-methyl-3-(phenylsulfanyl)naphthoquinone
• CAS NO: 70691-68-8
• Molecular Formula: C₁₇H₁₂O₂S
• Molecular Weight: 280.34098
• Mol File: 70691-68-8.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-methyl-3-(phenylsulfanyl)naphthoquinone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methyl-3-(phenylsulfanyl)naphthoquinone(70691-68-8)
• EPA Substance Registry System: 2-methyl-3-(phenylsulfanyl)naphthoquinone(70691-68-8)

Safety Data

• Hazardous Substances Data: 70691-68-8(Hazardous Substances Data)

Upstream product

• 58-27-5 menadione 
• 882-33-7 diphenyldisulfane 
• 15448-59-6 2,3-epoxy-2-methyl-2,3-dihydro-1,4-naphthoquinone 
• 108-98-5 thiophenol 
• 3129-39-3 2-bromo-3-methyl-[1,4]naphthoquinone 

Relevant articles and documents

Heterocyclic effect for optical properties of naphthoquinone-based pigment: 2-methyl-3-heteroarylthio-1,4-naphthalenedione

Three novel naphthoquinone-based heterocyclic pigments, 2-methyl-3-[(1-methyl-1H-imidazol-2-yl)thio-1,4-naphthalenedione, (4-methyl-4H-1,2,4-triazol-3-yl)thio-1,4-naphthalenedione, and (1-methyl-1H-tetrazol-5-yl)thio]-1,4-naphthalenedione, are synthesized, and their optical properties in both solution and solid states are investigated. Depending on the heteroarylthio ring in the pigment, variation in optical properties is observed, e.g. characteristic colours for each pigment in the solution and solid states. The achiral pigment containing the 1-methyl-1H-tetrazol-5-yl ring exhibits a chiral space group and a CD signal in the solid state.

Silver-Catalyzed Direct Thiolation of Quinones by Activation of Aryl Disulfides to Synthesize Quinonyl Aryl Thioethers

A silver-catalyzed coupling reaction of quinones with aryl disulfides for the synthesis of quinonyl aryl thioethers is described. In the presence of AgOAc (0.2 equiv)/dppp (0.24 equiv) as the catalyst, (NH4)2S2O8/sub

Synthesis and selective anticancer activity of organochalcogen based redox catalysts

Many tumor cells exhibit a disturbed intracellular redox state resulting in higher levels of reactive oxygen species (ROS). As these contribute to tumor initiation and sustenance, catalytic redox agents combining significant activity with substrate specif