187851-83-8

Basic information

• Product Name: (S)-1-{(R)-2-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-4-methyl-pentanoyloxy]-3-phenyl-propionyl}-piperidine-2-carboxylic acid (R)-1-benzyloxycarbonyl-ethyl ester
• Synonyms: (S)-1-{(R)-2-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-4-methyl-pentanoyloxy]-3-phenyl-propionyl}-piperidine-2-carboxylic acid (R)-1-benzyloxycarbonyl-ethyl ester
• CAS NO: 187851-83-8
• Molecular Weight: 666.812
• Mol File: 187851-83-8.mol

Chemical Properties

• CAS DataBase Reference: (S)-1-{(R)-2-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-4-methyl-pentanoyloxy]-3-phenyl-propionyl}-piperidine-2-carboxylic acid (R)-1-benzyloxycarbonyl-ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-{(R)-2-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-4-methyl-pentanoyloxy]-3-phenyl-propionyl}-piperidine-2-carboxylic acid (R)-1-benzyloxycarbonyl-ethyl ester(187851-83-8)
• EPA Substance Registry System: (S)-1-{(R)-2-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-4-methyl-pentanoyloxy]-3-phenyl-propionyl}-piperidine-2-carboxylic acid (R)-1-benzyloxycarbonyl-ethyl ester(187851-83-8)

Safety Data

• Hazardous Substances Data: 187851-83-8(Hazardous Substances Data)

Upstream product

• 26250-84-0 (S)-(-)-1-(tert-butoxycarbonyl)-2-piperidinecarboxylic acid 
• 187851-81-6 (S)-Piperidine-1,2-dicarboxylic acid 2-((R)-1-benzyloxycarbonyl-ethyl) ester 1-tert-butyl ester 
• 56777-24-3 benzyl (S)-Lactate 
• 153052-71-2 Boc-L-MeLeu-D-PhLac-OH 
• 187851-82-7 benzyl L-pipecolyl-D-lactate 

Downstream Products

• 187851-84-9 (S)-1-{(R)-2-[(S)-2-(tert-Butoxycarbonyl-methyl-amino)-4-methyl-pentanoyloxy]-3-phenyl-propionyl}-piperidine-2-carboxylic acid (R)-1-carboxy-ethyl ester 

Relevant articles and documents

Generation of a small library of cyclodepsipeptide PF1022A analogues using a cyclization-Cleavage method with oxime resin

N-Methyloctadepsipeptides attached to an oxime resin were cyclized by heating them in refluxing ethyl acetate for 2 days to give cyclodepsipeptide PF1022A analogues. By using this method, we generated a small library of PF 1022A analogues (2), several of which possessed anthelmintic activity, based on an in vitro assay.