27064-08-0

Basic information

• Product Name: S-p-tolyl methanethioate
• Synonyms: S-p-tolyl methanethioate
• CAS NO: 27064-08-0
• Molecular Weight: 152.217
• Mol File: 27064-08-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: S-p-tolyl methanethioate(CAS DataBase Reference)
• NIST Chemistry Reference: S-p-tolyl methanethioate(27064-08-0)
• EPA Substance Registry System: S-p-tolyl methanethioate(27064-08-0)

Safety Data

• Hazardous Substances Data: 27064-08-0(Hazardous Substances Data)

Upstream product

• 3112-85-4 methylphenylsulfonate 
• 103-19-5 di(p-tolyl) disulfide 
• 1427290-04-7 1-(phenylseleno)-1,1-(S_S,S_S)-bis(p-tolylsulfinyl)methane 
• 5707-04-0 Phenylselenyl chloride 
• 59532-34-2 (S_S,S_S)-1,1-bis(p-tolylsulfinyl)methane 
• 64-18-6 formic acid 
• 39549-10-5 1-[(4-methylphenyl)sulfanyl]pyrrolidine-2,5-dione 
• 6317-27-7 p-chlorophenyl mesylate 
• 106-45-6 para-thiocresol 

Downstream Products

• 36160-34-6 Cl₂CHSC₆H₄Me-p 
• 2976-38-7 p-tolyltrichloromethylsulfide 

Relevant articles and documents

The preparation of thiol formates

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Thioimides: New reagents for effective synthesis of thiolesters from carboxylic acids

(Chemical Equation Presented) Thioimides and carboxylic acids are used as the precursors for the convenient synthesis of thiolesters in the phosphine mediated process. Cyclic and acyclic thioimides show equal efficiency, furnishing the desired thiolesters in good to excellent yields. The general, highly efficient transformation tolerates various functional groups and the resulting thiolesters are obtained in high purity after a simple separation. The reaction scope has been demonstrated on the preparation of several highly functionalized target molecules.