1312929-67-1

Basic information

• Product Name: (2S,3S)-1,1-diethyl 3-methyl 3-(diphenylmethyleneamino)-2-(furan-2-yl)propane-1,1,3-tricarboxylate
• Synonyms: (2S,3S)-1,1-diethyl 3-methyl 3-(diphenylmethyleneamino)-2-(furan-2-yl)propane-1,1,3-tricarboxylate
• CAS NO: 1312929-67-1
• Molecular Weight: 491.541
• Mol File: 1312929-67-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S,3S)-1,1-diethyl 3-methyl 3-(diphenylmethyleneamino)-2-(furan-2-yl)propane-1,1,3-tricarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S)-1,1-diethyl 3-methyl 3-(diphenylmethyleneamino)-2-(furan-2-yl)propane-1,1,3-tricarboxylate(1312929-67-1)
• EPA Substance Registry System: (2S,3S)-1,1-diethyl 3-methyl 3-(diphenylmethyleneamino)-2-(furan-2-yl)propane-1,1,3-tricarboxylate(1312929-67-1)

Safety Data

• Hazardous Substances Data: 1312929-67-1(Hazardous Substances Data)

Upstream product

• 17448-96-3 ethyl 2-carbethoxy-3-(2-furanyl)propenoate 
• 81167-39-7 methyl N-(diphenylmethylene)glycinate 

Relevant articles and documents

Enantiocontrolled synthesis of β-branched α-amino acids by using CuI-catalyzed 1,4-addition of glycine imines to β-substituted gem-diactivated olefins

Branching out! The catalytic asymmetric conjugate addition of glycinate Schiff bases to β-substituted gem-diactivated Michael acceptors under proton transfer conditions gives a variety of β-branched α-amino acids (see scheme; Dpm=diphenylmethylene, EWG=electron-withdrawing group) with excellent levels of diastereo- (typically syn/anti >90:10) and enantiocontrol (90-99 % ee). Copyright