51514-13-7

Basic information

• Product Name: L-Tyrosine, N-[(phenylmethoxy)carbonyl]-, acetate (ester)
• CAS NO: 51514-13-7
• Molecular Formula: C19H19NO6
• Molecular Weight: 357.363
• Mol File: 51514-13-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: L-Tyrosine, N-[(phenylmethoxy)carbonyl]-, acetate (ester)(CAS DataBase Reference)
• NIST Chemistry Reference: L-Tyrosine, N-[(phenylmethoxy)carbonyl]-, acetate (ester)(51514-13-7)
• EPA Substance Registry System: L-Tyrosine, N-[(phenylmethoxy)carbonyl]-, acetate (ester)(51514-13-7)

Safety Data

• Hazardous Substances Data: 51514-13-7(Hazardous Substances Data)

Upstream product

• 13512-31-7 N-(benzyloxycarbonyl)-L-tyrosine methyl ester 
• 16679-94-0 N-[(phenylmethoxy)carbonyl]-L-tyrosine 
• 1164-16-5 Z-L-Tyr-OH 
• 108-24-7 acetic anhydride 

Downstream Products

• 916162-44-2 O-acetyl-N-benzyloxycarbonyl-L-tyrosine methyl ester 
• 23224-65-9 L-Tyr(OAc) NCA 
• 6636-22-2 O-acetyl-L-tyrosine 
• 51514-08-0 O-acetyl-N-benzyloxycarbonyl-L-tyrosyl chloride 
• 102948-17-4 O-acetyl-N-benzyloxycarbonyl-L-tyrosine-(4-nitro-benzyl ester) 
• 174743-68-1 O-acetyl-N-benzyloxycarbonyl L-tyrosyl D-lactic acid t-butyl ester 
• 519156-40-2 (S)-3-benzyloxycarbonyl-4-(4-acetoxybenzyl)oxazolidin-5-one 
• 174743-70-5 benzyloxycarbonyl D-phenylalanyl L-α-hydroxyisovaleryl-O-acetyl L-tyrosyl D-lactic acid t-butyl ester 
• 174743-71-6 D-phenylalanyl L-α-hydroxyisovaleryl O-acetyl L-tyrosyl D-lactic acid t-butyl ester 
• 618116-00-0 N-benzyloxycarbonyl-L-tyrosyl-L-tyrosyl-L-tyrosine 
• 7390-78-5 L-tyrosyl-L-tyrosyl-L-tyrosine 
• 64730-64-9 4-acetoxytyrosine methyl ester 
• 109068-84-0 O-acetyl-L-tyrosine-(4-nitro-benzyl ester); hydrobromide 
• 21778-69-8 tyrosylglycylglycine 

Relevant articles and documents

Synthesis of novel potassium selective valinomycins

The synthesis is described of three aryl substituted valinomycins, in which the aryl groups are placed around the poles of the cyclodepsipeptide. In one synthesis a valinomycin is prepared carrying a pendant hydroxyphenyl residue. In this synthesis the use of the acetate functionality to protect the phenolic site in tyrosine is developed. The spectroscopic and electrochemical evidence indicating the potential importance of such modified valinomycins in the design of improved ion selective electrodes is discussed.