21132-20-7

Basic information

• Product Name: Phenylalanine, N-acetyl-a-cyano-, ethyl ester
• CAS NO: 21132-20-7
• Molecular Formula: C14H16N2O3
• Molecular Weight: 260.293
• Mol File: 21132-20-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Phenylalanine, N-acetyl-a-cyano-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Phenylalanine, N-acetyl-a-cyano-, ethyl ester(21132-20-7)
• EPA Substance Registry System: Phenylalanine, N-acetyl-a-cyano-, ethyl ester(21132-20-7)

Safety Data

• Hazardous Substances Data: 21132-20-7(Hazardous Substances Data)

Upstream product

• 100-44-7 benzyl chloride 
• 90877-70-6 ethyl 2-acetamido-2-cyanoacetate 
• 1024-41-5 benzyl tosylate 
• 32683-02-6 ethyl-2-aminocyano acetate 
• 100-39-0 benzyl bromide 

Downstream Products

• 31603-06-2 1-(5-Tetrazolyl)-2-phenylethylamin 
• 150-30-1 Phenylalanine 
• 109570-13-0 2-acetylamino-3-phenyl-2-(1H-tetrazol-5-yl)-propionic acid ethyl ester 
• 114477-72-4 8-Benzyl-6-methyl-2-thioxo-2,3-dihydro-1H-imidazo[1,5-a][1,3,5]triazin-4-one 
• 114477-71-3 N-(4-Amino-5-benzyl-6-oxo-2-thioxo-1,2,5,6-tetrahydro-pyrimidin-5-yl)-acetamide 
• 108921-94-4 N-[2-phenyl-1-(1H-tetrazol-5-yl)-ethyl]-acetamide 
• 5619-07-8 methyl 2-amino-3-phenylpropanoate hydrochloride 
• 111753-78-7 Phe-O-butyl ester hydrochloride 
• 21156-62-7 N-acetylphenylalanine methyl ester 
• 194661-20-6 butyl 2-acetylamino-3-phenylpropanoate 
• 1575605-52-5 allyl 2-acetylamino-3-phenylpropanoate 
• 3618-96-0 (S)-N-acetylphenylalanine 
• 21156-62-7 (R)-N-acetylphenylalanine methyl ester 
• 2361-98-0 butyl 2-acetylamino-3-phenylpropanoate 

Relevant articles and documents

Oxovanadium(IV) Schiff base complex derived from phenylalanine analogue containing 2,3-diaminopropionic acid (DAP): Synthesis, computational study, and biological evaluation

Reduced Schiff base ligand by condensation of phenylalanine analogue containing 2,3-diaminopropionic acid (DAP) with salicylaldehyde and its oxovanadium(IV) complex have been prepared. Chemical and structural properties were fully characterized. Density f

Tetrazole analogs of phenylalanine derivatives as tyrosine hydroxylase inhibitors

Eight new tetrazole analogs of phenylalanine derivatives in which the carboxyl group was replaced by a tetrazole ring were synthesized. At a concentration of 2.5 x 10-5 M, each compound exhibited greater than 50% inhibition of tyrosine hydroxylase activity.