36325-39-0

Basic information

• Product Name: Methanethioamide, N-methyl-N-phenyl-
• CAS NO: 36325-39-0
• Molecular Formula: C8H9NS
• Molecular Weight: 151.232
• Mol File: 36325-39-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Methanethioamide, N-methyl-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanethioamide, N-methyl-N-phenyl-(36325-39-0)
• EPA Substance Registry System: Methanethioamide, N-methyl-N-phenyl-(36325-39-0)

Safety Data

• Hazardous Substances Data: 36325-39-0(Hazardous Substances Data)

Upstream product

• 93-61-8 N-methyl-N-phenylformamide 

Downstream Products

• 93-61-8 N-methyl-N-phenylformamide 
• 19009-45-1 N-methyl-N-phenylthiocarbamoyl chloride 
• 35452-42-7 C₈H₈BrNS 
• 59408-51-4 2-Hydroxy-N-methyl-2,2,N-triphenyl-thioacetamide 

Relevant articles and documents

Amide (A)–thioamide (T) interconversions using Ph3SiSH (A to T) and Ph3SnOH (T to A) reagents

Ph3SiSH transforms amides to thioamides and Ph3SnOH performs the reverse process, with the concomitant formation of Ph3SiOH (or Ph3SiOSiPh3) and Ph3SnSSnPh3, respectively. The chemistry is a delightful illustration of the oxophilicity of silicon compared to the thiophilicity of tin and occurs under relatively mild conditions, and for amide to thioamide transformation requires no amide activation. The chemistry is in accord with available data for Si?(S)(O), Sn?(O)(S) and C?(O)(S) bond energies. Copyright

Studies on organophosphorus compounds. XXI. The dimer of p-methoxyphenylthionophosphine sulfide as thiation reagent. A new route to thiocarboxamides

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