942066-16-2

Basic information

• Product Name: C₆H₄C₂H₃NSO₂C₇H₇OCH₃
• Synonyms: C₆H₄C₂H₃NSO₂C₇H₇OCH₃
• CAS NO: 942066-16-2
• Molecular Weight: 303.382
• Mol File: 942066-16-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₆H₄C₂H₃NSO₂C₇H₇OCH₃(CAS DataBase Reference)
• NIST Chemistry Reference: C₆H₄C₂H₃NSO₂C₇H₇OCH₃(942066-16-2)
• EPA Substance Registry System: C₆H₄C₂H₃NSO₂C₇H₇OCH₃(942066-16-2)

Safety Data

• Hazardous Substances Data: 942066-16-2(Hazardous Substances Data)

Upstream product

• 6873-55-8 p-tolylsulfinyl amide 
• 579-74-8 2-Methoxyacetophenone 

Downstream Products

• 93027-83-9 N-(1-(2-methoxyphenyl)ethyl)-4-methylbenzenesulfonamide 

Relevant articles and documents

Highly enantioselective Pd-catalyzed asymmetric hydrogenation of activated imines

(Chemical Equation Presented) Pd/bisphosphines complexes are highly effective catalysts for asymmetric hydrogenation of activated imines in trifluoroethanol. The asymmetric hydrogenation of N-diphenylphosphinyl ketimines 3 with Pd(CF3CO2)/(S)-SegPhos indicated 87-99% ee, and N-tosylimines 5 could gave 88-97% ee with Pd-(CF3CO 2)/(S)-SynPhos as a catalyst. Cyclic N-sulfonylimines 7 and 11 were hydrogenated to afford the useful chiral sultam derivatives in 79-93% ee, which are important organic synthetic intermediates and structural units of agricultural and pharmaceutical agents.