930118-37-9

Basic information

• Product Name: 4-methoxy-2,3,6-trimethyl-N-[3-methyl-1-(toluene-4-sulfonyl)-butyl]-benzenesulfonamide
• Synonyms: 4-methoxy-2,3,6-trimethyl-N-[3-methyl-1-(toluene-4-sulfonyl)-butyl]-benzenesulfonamide
• CAS NO: 930118-37-9
• Molecular Weight: 453.624
• Mol File: 930118-37-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-methoxy-2,3,6-trimethyl-N-[3-methyl-1-(toluene-4-sulfonyl)-butyl]-benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methoxy-2,3,6-trimethyl-N-[3-methyl-1-(toluene-4-sulfonyl)-butyl]-benzenesulfonamide(930118-37-9)
• EPA Substance Registry System: 4-methoxy-2,3,6-trimethyl-N-[3-methyl-1-(toluene-4-sulfonyl)-butyl]-benzenesulfonamide(930118-37-9)

Safety Data

• Hazardous Substances Data: 930118-37-9(Hazardous Substances Data)

Upstream product

• 80745-07-9 4-methoxy-2,3,6-trimethylbenzenesulfonyl chloride 
• 697-82-5 2,3,5-trimethylphenol 
• 20469-61-8 2,3,5-trimethylanisole 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 590-86-3 isovaleraldehyde 
• 316831-31-9 4-methoxy-2,3,6-trimethylbenzenesulfonamide 

Relevant articles and documents

Advantage of in situ generation of N-arylsulfonyl imines from α-amide sulfones in the phase-transfer-catalyzed asymmetric Strecker reaction

Highly efficient, catalytic enantioselective synthesis of N-arylsulfonyl α-amino nitriles from the corresponding α-amido sulfones has been achieved under toluene-aqueous potassium cyanide biphasic conditions using chiral quaternary ammonium iodide (R,R,R)-1 as an effective phase-transfer catalyst. This Strecker synthesis involving the in situ generation of the reactive N-sulfonyl imines is advantageous for the cyanation of the substrates having primary and secondary alkyl substituents.