1372996-81-0

Basic information

• Product Name: (3S,4S)-3-(4-methoxyphenyl)-4,6-diphenyl-1-tosyl-3,4-dihydropyridin-2(1H)-one
• CAS NO: 1372996-81-0
• Molecular Weight: 509.626
• Mol File: 1372996-81-0.mol

Chemical Properties

• CAS DataBase Reference: (3S,4S)-3-(4-methoxyphenyl)-4,6-diphenyl-1-tosyl-3,4-dihydropyridin-2(1H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: (3S,4S)-3-(4-methoxyphenyl)-4,6-diphenyl-1-tosyl-3,4-dihydropyridin-2(1H)-one(1372996-81-0)
• EPA Substance Registry System: (3S,4S)-3-(4-methoxyphenyl)-4,6-diphenyl-1-tosyl-3,4-dihydropyridin-2(1H)-one(1372996-81-0)

Safety Data

• Hazardous Substances Data: 1372996-81-0(Hazardous Substances Data)

Upstream product

• 358621-92-8 N-(p-tolylsulfonyl)-1,3-diphenyl-2-propen-1-imine 
• 4693-91-8 4-methoxyphenyl-acetic chloride 
• 104-01-8 4-Methoxyphenylacetic acid 

Relevant articles and documents

An Upstream By-product from Ester Activation via NHC-Catalysis Catalyzes Downstream Sulfonyl Migration Reaction

A sequential reaction combining N-heterocyclic carbene (NHC) and N-hydroxyphthalimide (NHPI) catalysis allowed for the upstream by-product NHPI, which was generated in the NHC-catalyzed cycloaddition reaction, to act as the catalyst for a downstream nitro

Enantioselective activation of stable carboxylate esters as enolate equivalents via N-heterocyclic carbene catalysts

The first N-Heterocyclic Carbene (NHC) mediated activation of stable carboxylate esters to generate enolate intermediates is disclosed. The catalytically generated arylacetic ester enolates undergo enantioselective reactions with α,β-unsaturated imines.