58848-63-8

Basic information

• Product Name: D-phenylalanine p-nitrophenyl ester
• Synonyms: D-phenylalanine p-nitrophenyl ester
• CAS NO: 58848-63-8
• Molecular Weight: 286.287
• Mol File: 58848-63-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: D-phenylalanine p-nitrophenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: D-phenylalanine p-nitrophenyl ester(58848-63-8)
• EPA Substance Registry System: D-phenylalanine p-nitrophenyl ester(58848-63-8)

Safety Data

• Hazardous Substances Data: 58848-63-8(Hazardous Substances Data)

Upstream product

• 75531-06-5 2-Decanoylamino-3-phenyl-propionic acid 4-nitro-phenyl ester 
• 2578-84-9 p-nitrophenyl N-(benzyloxycarbonyl)-L-phenylalaninate 
• 75531-06-5 2-Decanoylamino-3-phenyl-propionic acid 4-nitro-phenyl ester 
• 55895-89-1 D,L-phenylalanine p-nitrophenyl ester 
• 75531-07-6 p-nitrophenyl n-dodecanoyl-D(L)-phenylalaninate 
• 38806-34-7 p-Nitrophenyl 
• 14009-94-0 p-nitrophenyl N-acetyl-L-phenylalaninate 
• 14009-95-1 p-nitrophenyl N-acetyl-D-phenylalaninate 
• 2578-85-0 p-nitrophenyl N-(benzyloxycarbonyl)-D-phenylalaninate 

Downstream Products

• 100-02-7 4-nitro-phenol 
• 673-06-3 D-(R)-phenylalanine 
• 75531-11-2 N-dodecanoyl-L-phenylalanine 4-nitrophenylester 
• 75531-12-3 N-dodecanoyl-D-phenylalanine 4-nitrophenylester 
• 63-91-2 L-phenylalanine 
• 673-06-3 D-β-Phenyl-α-alanine 

Relevant articles and documents

Capillary electrophoretic separation of enantiomers of amino acids and amino acid derivatives using crown ether and cyclodextrin

The capillary zone electrophoresis using (+)-18-crown-6-tetracarbonic acid as a chiral selector was a suitable method for the enantiomeric separation of racemates of amino acids and of some amino acid derivatives (esters, dipeptides). The influence of the chemical structure of the compounds on the separation was investigated. After optimization of the separation conditions, baseline separations were obtained for most racemates. The addition of acetonitrile and TBAB yielded an improvement of the separation. Improved selectivity was further observed by the application of a cyclodextrin, HP-β-CD, in combination with the crown ether.

High Stereoselectivity in the Deacylation of p-Nitrophenyl N-Acylphenylalanates by Bilayer Vesicular Systems which include Dipeptide-type Nucleophiles

The deacylation of p-nitrophenyl N-acylphenylalanates with bilayer vesicular systems comprising dipeptide-type nucleophiles and a cationic double chain surfactant resulted in high stereoselectivity (kLcat/kDcat = 29.6 at 25 deg C and 83.6 at 10 deg C) for the deacylation of p-nitrophenyl N-dodecanoylphenylalanate by the catalytic system of N-(N-benzyloxycarbonyl-L-leucyl)-L-histidine and N,N-didodecyl-N,N-dimethylammonium bromide.