1309465-25-5

Basic information

• Product Name: (4S,5S)-methyl 5-(benzo[d][1,3]dioxol-5-yl)-1-(diphenylphosphinoyl)-4,5-dimethyl-2-thioxoimidazolidine-4-carboxylate
• CAS NO: 1309465-25-5
• Molecular Weight: 508.535
• Mol File: 1309465-25-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (4S,5S)-methyl 5-(benzo[d][1,3]dioxol-5-yl)-1-(diphenylphosphinoyl)-4,5-dimethyl-2-thioxoimidazolidine-4-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (4S,5S)-methyl 5-(benzo[d][1,3]dioxol-5-yl)-1-(diphenylphosphinoyl)-4,5-dimethyl-2-thioxoimidazolidine-4-carboxylate(1309465-25-5)
• EPA Substance Registry System: (4S,5S)-methyl 5-(benzo[d][1,3]dioxol-5-yl)-1-(diphenylphosphinoyl)-4,5-dimethyl-2-thioxoimidazolidine-4-carboxylate(1309465-25-5)

Safety Data

• Hazardous Substances Data: 1309465-25-5(Hazardous Substances Data)

Upstream product

• 921936-94-9 C₂₁H₁₈NO₃P 
• 26349-74-6 2-isothiocyanatopropionic acid methyl ester 

Relevant articles and documents

Stereodivergent direct catalytic asymmetric mannich-type reactions of α-isothiocyanato ester with ketimines

Now accessible: Sterically hindered vicinal tetrasubstituted carbon stereocenters, which are not accessible by asymmetric hydrogenation, were constructed by a catalytic asymmetric C-C bond formation (see scheme; Dpp=diphenylphosphinoyl). By changing the Group 2 metal center, stereodivergent access to α,β-tetrasubstituted α,β-diamino esters was realized. Copyright