74392-86-2

Basic information

• Product Name: N-(tert-butyloxycarbonyl)-L-tyrosyl-D-alanine methyl ester
• Synonyms: N-(tert-butyloxycarbonyl)-L-tyrosyl-D-alanine methyl ester
• CAS NO: 74392-86-2
• Molecular Weight: 366.414
• Mol File: 74392-86-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-(tert-butyloxycarbonyl)-L-tyrosyl-D-alanine methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: N-(tert-butyloxycarbonyl)-L-tyrosyl-D-alanine methyl ester(74392-86-2)
• EPA Substance Registry System: N-(tert-butyloxycarbonyl)-L-tyrosyl-D-alanine methyl ester(74392-86-2)

Safety Data

• Hazardous Substances Data: 74392-86-2(Hazardous Substances Data)

Upstream product

• 14316-06-4 D-alanine methyl ester hydrochloride 
• 74825-83-5 Boc-(L)(α-Me)Tyr-OH 
• 3978-80-1 Boc-Tyr-OH 

Downstream Products

• 74392-87-3 Boc Tyr D_.Ala Gly Phe Leu OMe 
• 66960-03-0 Boc Tyr D_.Ala Gly Phe Met NH₂ 
• 74392-85-1 Boc Tyr D_.Ala Gly Phe Leu NH₂ 
• 66444-26-6 Methyl tert-butyloxycarbonyltyrosyl-(D)alanylglycylphenylalaninate 
• 66864-07-1 Tyr D_.Ala Gly Phe Pro NH₂ 
• 74108-23-9 Tyr D_.Ala Gly (6H)Phe Pro NH₂ 
• 67582-10-9 Boc Tyr D_.Ala Gly Phe OH 
• 67581-53-7 N-(tert-butyloxycarbonyl)-L-tyrosyl-D-alanylglycyl-L-phenylalanyl-L-methionine methyl ester 
• 65189-64-2 H-Tyr-D-Ala-Gly-Phe-Leu-NH₂ 
• 61090-95-7 (S)-2-[(S)-2-(2-{(R)-2-[(S)-2-Amino-3-(4-hydroxy-phenyl)-propionylamino]-propionylamino}-acetylamino)-3-phenyl-propionylamino]-4-methylsulfanyl-butyramide 
• 71591-34-9 N-(tert-butyloxycarbonyl)-L-tyrosyl-D-alanine 
• 153716-13-3 Ac-L-Tyr-D-Ala-OMe 
• 83049-21-2 (L,D)-Ac-Tyr(Ac)-D-Ala-OMe 
• 78537-11-8 N-(tert-butyloxycarbonyl)-L-tyrosyl-D-alanylglycyl-L-phenylalanyl-L-methionyl-O-tert-butyl-L-threonine methyl ester 

Relevant articles and documents

5(4H)-oxazolones as intermediates in the carbodiimide- and cyanamide-promoted peptide activations in aqueous solution

The early days: Although considered a species to be avoided in peptide chemistry, the intermediacy of 5(4H)-oxazolones is demonstrated to be essential for the formation of peptides through cyanamide and carbodiimide activation in aqueous solution (see sch

NUCLEO AMINO ACIDS AND NUCLEOPEPTIDES. XII. SYNTHESIS AND PROPERTIES OF ADENINYLALANINE ANALOGS OF LEUCINE-5-ENKEPHALIN

-

Synthesis and pharmacological study of some enkephalin analogs in relation to the plurality of opiate receptors

We have synthesized a series of enkephalin analogs and measured their affinity for each type of 'opiate' receptor, the μ receptor and the δ receptor. Furthermore, we have determined their respective antinociceptive activity after intracerebroventricular i