37888-21-4

Basic information

• Product Name: L-Phenylalanine, N-[(2,2,2-trichloroethoxy)carbonyl]-
• CAS NO: 37888-21-4
• Molecular Formula: C12H12Cl3NO4
• Molecular Weight: 340.591
• Mol File: 37888-21-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: L-Phenylalanine, N-[(2,2,2-trichloroethoxy)carbonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: L-Phenylalanine, N-[(2,2,2-trichloroethoxy)carbonyl]-(37888-21-4)
• EPA Substance Registry System: L-Phenylalanine, N-[(2,2,2-trichloroethoxy)carbonyl]-(37888-21-4)

Safety Data

• Hazardous Substances Data: 37888-21-4(Hazardous Substances Data)

Upstream product

• 63-91-2 L-phenylalanine 
• 17341-93-4 2,2,2-Trichloroethyl chloroformate 
• 100821-64-5 1,2,2,2-Tetrachloroethyl 2,2,2-trichloroethyl carbonate 
• 75-77-4 chloro-trimethyl-silane 
• 66065-85-8 succinimidyl 2,2,2-trichloroethyl carbonate 

Downstream Products

• 78221-42-8 (S)-2-((S)-2-Amino-3-phenyl-propionylamino)-4-methylsulfanyl-butyric acid ethyl ester; hydrochloride 
• 78221-38-2 (S)-4-Methylsulfanyl-2-[(S)-3-phenyl-2-(2,2,2-trichloro-ethoxycarbonylamino)-propionylamino]-butyric acid ethyl ester 

Relevant articles and documents

RENIN INHIBITING COMPOUNDS

Compounds which are amino acid derivatives and have the formula STR1 in which R 1 is hydrogen or methyl, R 2 is ethyl, propyl or imidazol-4-yl, R 3 is isobutyl, cyclohexylmethyl or benzyl, and A is defined as herein are useful as renin inhibitors.

Alkyl 1-Chloroalkyl Carbonates: Reagents for the Synthesis of Carbamates and Protection of Amino Groups

The synthesis of 1-chloroalkyl carbonates and their reaction with various type of amines are described.This reaction is useful for the synthesis of carbamate pesticides and for the protection of various amino groups, including amino acids.

N-2,2,2-Trichloroethoxycarbonyl-L-amino Acids

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