187851-81-6

Basic information

• Product Name: (S)-Piperidine-1,2-dicarboxylic acid 2-((R)-1-benzyloxycarbonyl-ethyl) ester 1-tert-butyl ester
• Synonyms: (S)-Piperidine-1,2-dicarboxylic acid 2-((R)-1-benzyloxycarbonyl-ethyl) ester 1-tert-butyl ester
• CAS NO: 187851-81-6
• Molecular Weight: 391.464
• Mol File: 187851-81-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (S)-Piperidine-1,2-dicarboxylic acid 2-((R)-1-benzyloxycarbonyl-ethyl) ester 1-tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-Piperidine-1,2-dicarboxylic acid 2-((R)-1-benzyloxycarbonyl-ethyl) ester 1-tert-butyl ester(187851-81-6)
• EPA Substance Registry System: (S)-Piperidine-1,2-dicarboxylic acid 2-((R)-1-benzyloxycarbonyl-ethyl) ester 1-tert-butyl ester(187851-81-6)

Safety Data

• Hazardous Substances Data: 187851-81-6(Hazardous Substances Data)

Upstream product

• 3105-95-1 pipecolinic acid 
• 33106-32-0 (S)-2-(benzyloxy)propanoic acid 
• 26250-84-0 (S)-(-)-1-(tert-butoxycarbonyl)-2-piperidinecarboxylic acid 
• 24424-99-5 di-tert-butyl dicarbonate 
• 56777-24-3 benzyl (S)-Lactate 

Downstream Products

• 187851-87-2 N-methyl-L-leucyl-3-phenyl-D-lactyl-N-methyl-L-leucyl-D-lactyl-N-methyl-L-leucyl-3-phenyl-D-lactyl-L-pipecolyl-D-lactic acid 
• 188908-43-2 1-[2-(4-methyl-2-{methyl-[2-(4-methyl-2-{methyl-[2-(4-methyl-2-methylamino-pentanoyloxy)-3-phenyl-propionyl]-amino}-pentanoyloxy)-propionyl]-amino}-pentanoyloxy)-3-phenyl-propionyl]-piperidine-2-carboxylic acid 1-benzyloxycarbonyl-ethyl ester 
• 188908-42-1 C₆₃H₈₈N₄O₁₅ 
• 187851-83-8 (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 
• 187851-84-9 (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 
• 187851-82-7 benzyl L-pipecolyl-D-lactate 

Relevant articles and documents

Solid-phase synthesis of cyclooctadepsipeptide PF1022A analogs using a cyclization-cleavage method with grime resin

N-Methyloctadepsipeptides attached to an oxime resin were cyclized by heating them in refluxing ethyl acetate far 2 days to give cyclooctadepsipeptide PF1022A analogs.

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.