1253121-03-7

Basic information

• Product Name: (2R,4S)-4-(tert-butoxycarbonylamino)-4-phenylbutan-2-yl acetate
• Synonyms: (2R,4S)-4-(tert-butoxycarbonylamino)-4-phenylbutan-2-yl acetate
• CAS NO: 1253121-03-7
• Molecular Weight: 307.39
• Mol File: 1253121-03-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,4S)-4-(tert-butoxycarbonylamino)-4-phenylbutan-2-yl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,4S)-4-(tert-butoxycarbonylamino)-4-phenylbutan-2-yl acetate(1253121-03-7)
• EPA Substance Registry System: (2R,4S)-4-(tert-butoxycarbonylamino)-4-phenylbutan-2-yl acetate(1253121-03-7)

Safety Data

• Hazardous Substances Data: 1253121-03-7(Hazardous Substances Data)

Upstream product

• 876-27-7 4-chlorophenyl acetate 
• 528586-23-4 tert-butyl ((1S)-3-oxo-1-phenylbutyl)carbamate 

Downstream Products

• 1147347-28-1 (2R,4S)-4-(tert-butoxycarbonylamino)-4-phenylbutan-2-ol 

Relevant articles and documents

Enantioselective synthesis of syn - And anti -1,3-aminoalcohols via β-aminoketones and subsequent reduction/dynamic kinetic asymmetric transformation

β-Aminoketones obtained from imines in an organocatalytic Mannich reaction were transformed to enantio- and diastereomerically pure 1,3-aminoalcohols with two stereogenic centers via a combined reduction/dynamic kinetic asymmetric transformation. Both syn and anti diastereomers were obtained in high yield, dr, and ee.