39543-16-3

Basic information

• Product Name: Benzothiazole, 2-[(1,1-dimethylethyl)thio]- (9CI)
• Synonyms: Benzothiazole, 2-[(1,1-dimethylethyl)thio]- (9CI);2-(tert-Butylthio)benzothiazole;2-[(1,1-Dimethylethyl)thio]benzothiazole
• CAS NO: 39543-16-3
• Molecular Formula: C₁₁H₁₃NS₂
• Molecular Weight: 223.35762
• Product Categories: BENZOTHIAZOLE
• Mol File: 39543-16-3.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 325.6°Cat760mmHg
• Flash Point: 150.7°C
• Appearance: /
• Density: 1.19g/cm³
• Vapor Pressure: 0.000432mmHg at 25°C
• Refractive Index: 1.632
• CAS DataBase Reference: Benzothiazole, 2-[(1,1-dimethylethyl)thio]- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzothiazole, 2-[(1,1-dimethylethyl)thio]- (9CI)(39543-16-3)
• EPA Substance Registry System: Benzothiazole, 2-[(1,1-dimethylethyl)thio]- (9CI)(39543-16-3)

Safety Data

• Hazardous Substances Data: 39543-16-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H13NS2/c1-11(2,3)14-10-12-8-6-4-5-7-9(8)13-10/h4-7H,1-3H3

Upstream product

• 615-20-3 2-chlorobenzo[d][1,3]thiazole 
• 75-66-1 2-methylpropan-2-thiol 
• 6011-99-0 benzo[d]thiazol-2-yl thiocyanate 
• 677-22-5 tert-butylmagnesium chloride 
• 149-30-4 2-Mercaptobenzothiazole 
• 151484-28-5 1,1-dimethylethyl diphenylphosphinite 
• 75-15-0 carbon disulfide 
• 615-43-0 2-iodophenylamine 
• 149-30-4 2-thioxo-3H-1,3-benzothiazole 
• 71432-55-8 2-tert-butyl-1,3-diisopropylisourea 
• 95-16-9 1,3-Benzothiazole 
• 110-06-5 di-tert-butyl disulfide 
• 116928-25-7 benzo[d]thiazol-2-yltriphenylphosphonium trifluoromethanesulfonate 

Downstream Products

• 149-30-4 2-thioxo-3H-1,3-benzothiazole 

Relevant articles and documents

Selective C-H chalcogenation of thiazoles: Via thiazol-2-yl-phosphonium salts

Thiazoles and benzothiazoles undergo regioselective C2-H chalcogenation via the sequence of thiazole C2-functionalization with phosphines to produce phosphonium salts which in turn react with S- and Se-centered nucleophiles to give products of C2-H chalco

A novel synthesis of 2-alkylthiobenzothiazoles and 2-alkylthiobenzoxazoles

3H-Benzothiazole-2-thione and 3H-benzoxazole-2-thione were selectively S-alkylated by use of O-alkylisoureas as the alkylating reagents. The reactions could be performed under mild reaction conditions in short reaction times, and high yields were obtained using O-primary-alkylisoureas, whereas low yields were obtained with sec-and tert-alkylisoureas.

A new method for the preparation of alkyl aryl sulfides from alcohols via alkoxydiphenylphosphines by oxidation-reduction condensation

A new method for the preparation of alkyl aryl sulfides from alcohols via alkoxydiphenylphosphines by oxidation-reduction condensation was established. Various primary, secondary, and tertiary alcohols were successfully converted into the corresponding su