171038-43-0

Basic information

• Product Name: ethyl (2S,4R)-N-BOC-4-benzylprolinate
• Synonyms: ethyl (2S,4R)-N-BOC-4-benzylprolinate
• CAS NO: 171038-43-0
• Molecular Weight: 333.428
• Mol File: 171038-43-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ethyl (2S,4R)-N-BOC-4-benzylprolinate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl (2S,4R)-N-BOC-4-benzylprolinate(171038-43-0)
• EPA Substance Registry System: ethyl (2S,4R)-N-BOC-4-benzylprolinate(171038-43-0)

Safety Data

• Hazardous Substances Data: 171038-43-0(Hazardous Substances Data)

Upstream product

• 153080-85-4 ethyl (2S,4R)-1-(tert-butoxycarbonyl)-4-benzylpyroglutamate 

Downstream Products

• 183874-52-4 ethyl (4R)-4-benzylpyrroline-2-carboxylate 
• 170947-88-3 ethyl (4R)-N-(methoxycarbonyl)-4-benzyl-2,3-didehydroprolinate 
• 170947-89-4 diethyl <(2R,3S,4R)-N-(methoxycarbonyl)-4-benzyl-2-(ethoxycarbonyl)pyrrolidin-3-yl>malonate 
• 183874-63-7 (2R,3R,4R)-4-Benzyl-3-methyl-pyrrolidine-1,2-dicarboxylic acid 2-ethyl ester 1-methyl ester 
• 183874-54-6 (1R,4R,5R)-4-Benzyl-2-aza-bicyclo[3.1.0]hexane-1,2-dicarboxylic acid 1-ethyl ester 2-methyl ester 
• 183874-64-8 (2R,3S,4R)-4-Benzyl-3-phenyl-pyrrolidine-1,2-dicarboxylic acid 2-ethyl ester 1-methyl ester 
• 183874-60-4 (2R,3S,4R)-4-Benzyl-3-(1-ethoxycarbonyl-2-oxo-propyl)-pyrrolidine-1,2-dicarboxylic acid 2-ethyl ester 1-methyl ester 
• 183874-62-6 (2R,3R,4R)-4-Benzyl-3-(methoxycarbonyl-phenylsulfanyl-methyl)-pyrrolidine-1,2-dicarboxylic acid 2-ethyl ester 1-methyl ester 
• 183874-58-0 (2R,4R)-4-Benzyl-3-(bis-ethoxycarbonyl-methylene)-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester 
• 183874-61-5 (2R,3R,4R)-3-(Benzenesulfonyl-methoxycarbonyl-methyl)-4-benzyl-pyrrolidine-1,2-dicarboxylic acid 2-ethyl ester 1-methyl ester 
• 183874-57-9 (2R,3R,4R)-4-Benzyl-3-(bis-ethoxycarbonyl-phenylselanyl-methyl)-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester 

Relevant articles and documents

New enantioselective approach to α-allokainoids by Michael addition to chiral 4-substituted 2,3-didehydroprolinate

(-) and (+) α-Allokainoids hydrochlorides 3 and 4 were obtained by hydrolysis of the corresponding Michael adducts resulting from the addition of diethyl malonate to chiral N-urethane protected ethyl 4-benzyl-2,3-didehydroprolinates 9 and 13 respectively.