3507-54-8

Basic information

• Product Name: Benzothiazole, 2-(methylsulfinyl)- (7CI,8CI,9CI)
• Synonyms: Benzothiazole, 2-(methylsulfinyl)- (7CI,8CI,9CI)
• CAS NO: 3507-54-8
• Molecular Formula: C₈H₇NOS₂
• Molecular Weight: 197.27728
• Product Categories: BENZOTHIAZOLE
• Mol File: 3507-54-8.mol
• Article Data: 21

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzothiazole, 2-(methylsulfinyl)- (7CI,8CI,9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzothiazole, 2-(methylsulfinyl)- (7CI,8CI,9CI)(3507-54-8)
• EPA Substance Registry System: Benzothiazole, 2-(methylsulfinyl)- (7CI,8CI,9CI)(3507-54-8)

Safety Data

• Hazardous Substances Data: 3507-54-8(Hazardous Substances Data)

Upstream product

• 149-30-4 2-Mercaptobenzothiazole 
• 615-22-5 2-methylmercaptobenzothiazole 
• 119993-82-7 di-2-benzothiazolyl sulfoxide 
• 74-88-4 methyl iodide 

Downstream Products

• 95-16-9 1,3-Benzothiazole 
• 4271-09-4 2,2'-benzothiazolyl 
• 28908-00-1 (2-chloromethylthio)benzothiazole 
• 21564-17-0 2-(thiocyanomethylthio)benzothiazole 
• 934-34-9 2-hydroxybenzothiazole 
• 7144-49-2 2-methanesulfonylbenzothiazole 
• 615-22-5 2-methylmercaptobenzothiazole 

Relevant articles and documents

Kinetic Modelling of the catalytic oxidation of 2-(methylmercapto)-benzothiazole under mild conditions

2-(Methylmercapto)-benzothiazole oxidation was performed over Copper modified zeolites. The microporous materials were synthesized by the hydrothermal crystallization method and later modified with metal incorporation by wet impregnation. The solid cataly

Active potassium niobates and titanoniobates as catalysts for organic sulfide remediation

Pure (KNbO3) and titanium-substituted (KTi0.1Nb0.9O3 and KTi0.2Nb0.8O3) potassium niobates with perovskite crystalline structures were prepared, characterized and tested as catal

Selective and mild sulfoxidation of 2-sulfylbenzothiazole using hydroperoxides derived from cyclohexanone in the absence of catalyst

Alkyl hydroperoxides derived from cyclohexanone are attractive oxidants because they are easily available, more reactive than TBHP but much less acidic than m-CPBA. Wherein 1,1′-peroxybis(1-hydroperoxycyclohexane) (C) can be generated by the current simply method and displays the excellent reactivity and selectivity based on oxidative reactions of various benzothiazolyl sulfides substituted by different function groups. The research found that the reactions can be performed in the absence of catalyst and under very mild conditions optimized. Yields of sulfoxides is higher than 90%, no or a little reaction happened at the proximal double bond、 N and S atoms in the benzothiazolyl moiety. Phenyl sulfide as the substrates was also examined for the reaction scope test. The results show that they were uniquely and completely oxidized to sulfoxides in 1 h. A mild, environmentally friendly, catalyst-free aryl sulfide sulfoxidation method has been developed.

Highly Chemoselective and Enantioselective Catalytic Oxidation of Heteroaromatic Sulfides via High-Valent Manganese(IV)-Oxo Cation Radical Oxidizing Intermediates

A manganese complex with a porphyrin-like ligand that catalyzes the highly chemoselective and enantioselective oxidation of heteroaromatic sulfides, including imidazole, benzimidazole, indole, pyridine, pyrimidine, pyrazine, sym-triazine, thiophene, thiaz