31594-53-3

Basic information

• Product Name: 2-phenyl-3-carbomethoxy-3-methyl-Δ¹-pyrroline
• Synonyms: 2-phenyl-3-carbomethoxy-3-methyl-Δ¹-pyrroline
• CAS NO: 31594-53-3
• Molecular Weight: 217.268
• Mol File: 31594-53-3.mol

Chemical Properties

• CAS DataBase Reference: 2-phenyl-3-carbomethoxy-3-methyl-Δ¹-pyrroline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenyl-3-carbomethoxy-3-methyl-Δ¹-pyrroline(31594-53-3)
• EPA Substance Registry System: 2-phenyl-3-carbomethoxy-3-methyl-Δ¹-pyrroline(31594-53-3)

Safety Data

• Hazardous Substances Data: 31594-53-3(Hazardous Substances Data)

Upstream product

• 100-58-3 phenylmagnesium bromide 
• 80-62-6 methacrylic acid methyl ester 
• 7654-06-0 3-phenyl-2H-azirine 
• 103738-73-4 N-<1-(methylthio)benzylidene>-1-(trimethylsilyl)methylamine 

Relevant articles and documents

Silyl-Substituted Thioimidates as Nitrile Ylide Equivalents

Treatment of silyl-substituted thioimidates with silver fluoride in the presence of a trapping agent produces dipolar cycloadducts formally derived from nitrile ylides.The ratio of cycloadducts obtained from the reaction of unsymmetrically substituted dip

Regioselective Cycloadditions of N-Protonated Azomethine Ylides and 2-Azaallyl Anions Generated from N-(Silylmethyl) Thioimidates, Synthetic Equivalents of Nonstabilized Nitrile Ylides

A water-induced-desilylation method and a direct-desilylation method have been applied to N-(silylmethyl) thioimidates to lead to the generation of N-protonated azomethine ylides and 2-azaallyl anions, respectively.These reactive intermediates are capture

WATER-INDUCED AZOMETHINE YLIDE GENERATION FROM N-(SILYLMETHYL)THIOIMIDATES, SYNTHETIC EQUIVALENTS OF NONSTABILIZED NITRILE YLIDES

N-(Silylmethyl)thioimidates undergo a water-induced desilylation generating azomethine ylide 1,3-dipoles which cycloadd to a variety of electron-deficient olefins providing 1- or 2-pyrrolines after the elimination of thiol, indicating that the thioimidate