88854-18-6

Basic information

• Product Name: threo-O-Acetyl-N-acetyl-β-phenylserine ethyl ester
• Synonyms: threo-O-Acetyl-N-acetyl-β-phenylserine ethyl ester
• CAS NO: 88854-18-6
• Molecular Weight: 293.32
• Mol File: 88854-18-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: threo-O-Acetyl-N-acetyl-β-phenylserine ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: threo-O-Acetyl-N-acetyl-β-phenylserine ethyl ester(88854-18-6)
• EPA Substance Registry System: threo-O-Acetyl-N-acetyl-β-phenylserine ethyl ester(88854-18-6)

Safety Data

• Hazardous Substances Data: 88854-18-6(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 42267-16-3 (2S,3R)-2-amino-3-hydroxy-3-phenyl-propionic acid ethyl ester; hydrochloride 
• 60317-41-1 ethyl 2-(hydroxyimino)-3-oxo-3-phenylpropanoate 
• 15917-28-9 (2RS,3SR)-2-amino-3-hydroxy-3-phenyl-propionic acid ethyl ester 
• 69-96-5 dl-threo-phenylserine 
• 6966-29-6 N-acetyl-threo-DL-β-phenylserine ethyl ester 
• 6966-30-9 ethyl 2-acetamido-3-oxo-3-phenylpropanoate 
• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 98-86-2 acetophenone 

Downstream Products

• 5872-74-2 (2RS,3SR)-2-amino-3-hydroxy-3-(4-nitro-phenyl)-propionic acid 
• 4134-09-2 ethyl N-acetyl-DL-phenylalaninate 
• 33899-72-8 (2RS,3RS)-3-acetoxy-2-acetylamino-3-(4-nitro-phenyl)-propionic acid ethyl ester 
• 33899-72-8 (2RS,3SR)-3-acetoxy-2-acetylamino-3-(4-nitro-phenyl)-propionic acid ethyl ester 
• 3313-19-7 (1RS,2RS)-2-acetylamino-1-phenyl-propane-1,3-diol 
• 582295-24-7 (2S,3R)-2-amino-3-hydroxy-3-(4-nitro-phenyl)-propionic acid ethyl ester 

Relevant articles and documents

A Bulky Three-Hindered Quadrant Bisphosphine Ligand: Synthesis and Application in Rhodium-Catalyzed Asymmetric Hydrogenation of Functionalized Alkenes

A bulky three-hindered quadrant bisphosphine ligand, di-1-adamantylphosphino(tert-butylmethylphosphino)methane, named BulkyP*, has been synthesized via a convergent short pathway with chromatography-free procedures. The ligand is a crystalline solid and can be readily handled in air. Its rhodium(I) complex exhibits very high enantioselectivities and catalytic activities in the asymmetric hydrogenation of functionalized alkenes.