180254-00-6

Basic information

• Product Name: [N-[N'-(2-benzyloxycarbonyl)amino-2-methylpropionyl]-N-methylamino]acetic acid ethyl ester
• Synonyms: [N-[N'-(2-benzyloxycarbonyl)amino-2-methylpropionyl]-N-methylamino]acetic acid ethyl ester
• CAS NO: 180254-00-6
• Molecular Weight: 336.388
• Mol File: 180254-00-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: [N-[N'-(2-benzyloxycarbonyl)amino-2-methylpropionyl]-N-methylamino]acetic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [N-[N'-(2-benzyloxycarbonyl)amino-2-methylpropionyl]-N-methylamino]acetic acid ethyl ester(180254-00-6)
• EPA Substance Registry System: [N-[N'-(2-benzyloxycarbonyl)amino-2-methylpropionyl]-N-methylamino]acetic acid ethyl ester(180254-00-6)

Safety Data

• Hazardous Substances Data: 180254-00-6(Hazardous Substances Data)

Upstream product

• 15030-72-5 Z-Aib-OH 
• 52605-49-9 sarcosine ethyl ester hydrochloride 
• 13200-60-7 Sarcosine ethyl ester 
• 180253-99-0 (Methyl-phenylsulfanyl-amino)-acetic acid ethyl ester 
• 180253-97-8 2-Benzyloxycarbonylamino-2-methyl-propionic acid 2-thioxo-2H-pyridin-1-yl ester 

Downstream Products

• 741287-75-2 1,3,3-trimethylpiperazine-2,5-dione 

Relevant articles and documents

FIVE-MEMBERED HETEROCYCLIC DERIVATIVE

The present invention relates to a compound represented by formula (I): a salt of the compound, or a solvate of the compound or the salt; a drug containing any of the compounds, the salts, and the solvates; a preventive and/or therapeutic agent for an ischemic disease containing any of the compounds, the salts, and the solvates; and a platelet coagulation inhibitor containing any of the compounds, the salts, and the solvates. The compound of the present invention is useful as a strong platelet coagulation inhibitor without inhibiting COX-1 or COX-2.

N-hydroxypyridine-2(1H)-thione derivatives of carboxylic acids as activated esters. Part II. Applications in peptide synthesis

The N-hydroxypyridine-2(1H)-thione derivatives of two urethane-protected α-amino acids readily reacted with the α-amino acid esters or the corresponding benzenesulfenamides to give simple dipeptides in reasonable yields. The benzenesulfenamides are the re