79054-71-0

Basic information

• Product Name: N-tert-butyl-o-(methylthio)benzamide
• Synonyms: N-tert-butyl-o-(methylthio)benzamide
• CAS NO: 79054-71-0
• Molecular Weight: 223.339
• Mol File: 79054-71-0.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: N-tert-butyl-o-(methylthio)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-tert-butyl-o-(methylthio)benzamide(79054-71-0)
• EPA Substance Registry System: N-tert-butyl-o-(methylthio)benzamide(79054-71-0)

Safety Data

• Hazardous Substances Data: 79054-71-0(Hazardous Substances Data)

Upstream product

• 3724-10-5 2-(methylthio)benzoic acid 
• 75-64-9 tert-butylamine 
• 540-88-5 acetic acid tert-butyl ester 
• 6609-54-7 2-cyanothioanisole 
• 79894-26-1 N-Benzoyloxy-N-tert-butyl-2-methylsulfanyl-benzamide 
• 79894-32-9 N-t-butyl-2-(benzoyloxymethylthio)benzamide 
• 1442-03-1 2-methylsulfanyl-benzoyl chloride 

Downstream Products

• 79894-32-9 N-t-butyl-2-(benzoyloxymethylthio)benzamide 
• 79894-36-3 Acetic acid 2-tert-butylcarbamoyl-phenylsulfanylmethyl ester 
• 79054-65-2 N-t-butyl-2-(methylsulphinyl)benzamide 

Relevant articles and documents

An efficient method for the conversion of aromatic and aliphatic nitriles to the corresponding N-tert-butyl amides: A modified Ritter reaction

Aromatic and aliphatic nitriles react with tert-butyl acetate in the presence of a catalytic amount of sulfuric acid to give the corresponding N-tert-butyl amides in excellent yields.

Benzisothiazol-3-ones through a Metal-Free Intramolecular N–S Bond Formation

The highly efficient synthesis of benzoisothiazol-3-ones from thiobenzamides has been described with good functional group compatibility and excellent yields. This work represents the first example of selectfluor-promoted N–S bond formation processes. This method provides a facile approach to access various important bioactive benzoisothiazol-3-ones.

The thermal decomposition of N,O-diacyl-N-t-butylhydroxylamines. III. Novel routes to 2-substituted 1,2-benzisothiazol-3-(2H)-ones

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