1003577-32-9

Basic information

• Product Name: (3R,4R)-tert-butyl 3-hydroxy-4-(4-methoxyphenylamino)-pyrrolidine-1-carboxylate
• CAS NO: 1003577-32-9
• Molecular Weight: 308.378
• Mol File: 1003577-32-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (3R,4R)-tert-butyl 3-hydroxy-4-(4-methoxyphenylamino)-pyrrolidine-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (3R,4R)-tert-butyl 3-hydroxy-4-(4-methoxyphenylamino)-pyrrolidine-1-carboxylate(1003577-32-9)
• EPA Substance Registry System: (3R,4R)-tert-butyl 3-hydroxy-4-(4-methoxyphenylamino)-pyrrolidine-1-carboxylate(1003577-32-9)

Safety Data

• Hazardous Substances Data: 1003577-32-9(Hazardous Substances Data)

Upstream product

• 104-94-9 4-methoxy-aniline 
• 114214-49-2 1-tert-butoxycarbonyl-3,4-epoxypyrrolidine 

Relevant articles and documents

Synthesis of rare earth catalysts and their applications for enantioselective synthesis of heterocyclic β-amino alcohols

A new family of chiral lanthanide complexes derived from (R)-binaphthol has been synthesized by a one-pot procedure using only commercially available substrates. These complexes were evaluated for the aminolysis of meso-epoxides and proved to be efficient enantioselective catalysts. The samarium complex coordinated by two (R)-binaphthoxide ligands was the most enantioselective catalyst of this series. β-Amino alcohols including heterocycles have been isolated with enantiomeric excesses up to 84%.