30698-63-6

Basic information

• Product Name: 2,3-Dicyano-2-[4-(cyano-methoxycarbonyl-phenyl-methyl)-phenyl]-3-phenyl-succinic acid dimethyl ester
• CAS NO: 30698-63-6
• Molecular Weight: 521.529
• Mol File: 30698-63-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,3-Dicyano-2-[4-(cyano-methoxycarbonyl-phenyl-methyl)-phenyl]-3-phenyl-succinic acid dimethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-Dicyano-2-[4-(cyano-methoxycarbonyl-phenyl-methyl)-phenyl]-3-phenyl-succinic acid dimethyl ester(30698-63-6)
• EPA Substance Registry System: 2,3-Dicyano-2-[4-(cyano-methoxycarbonyl-phenyl-methyl)-phenyl]-3-phenyl-succinic acid dimethyl ester(30698-63-6)

Safety Data

• Hazardous Substances Data: 30698-63-6(Hazardous Substances Data)

Upstream product

• 30698-30-7 methyl 2-cyano-2-phenylacetate 
• 39095-38-0 N-dimethylsulfoniumsuccinimide chloride 

Relevant articles and documents

ADDITION NUCLEOPHILE DES ANIONS D'ESTERS α-CYANOACETIQUES SUR LES CATIONS SUCCINIMIDOSULFONIUM. FRAGMENTATION IONIQUE OU RADICALAIRE DES ?-SULFURANES INTERMEDIAIRES

Reactions of substituted cyanoacetate anions 4 with S,S-dialkylsuccinimidosulfonium salts resulted generally in the formation of N-alkylthiomethylketenimines and α-alkylthiomethylesters.Coupling products were also obtained with anion 4d and only observed in the case of methyl phenylcyanoacetate anion 4b.The results were interpreted by the formation of instable ?-sulfurane intermediates.Homolytic cleavage of these intermediates gave radical pairs, then the coupling products.Heterolytic cleavage gave new sulfonium salts which rearranged via sulfonium ylides.