114717-06-5

Basic information

• Product Name: L-Proline, 3-hydroxy-5-methyl-, (3R,5R)- (9CI)
• Synonyms: L-Proline, 3-hydroxy-5-methyl-, (3R,5R)- (9CI)
• CAS NO: 114717-06-5
• Molecular Formula: C6H11NO3
• Molecular Weight: 145.15644
• Product Categories: CARBOXYLICACID
• Mol File: 114717-06-5.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: L-Proline, 3-hydroxy-5-methyl-, (3R,5R)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: L-Proline, 3-hydroxy-5-methyl-, (3R,5R)- (9CI)(114717-06-5)
• EPA Substance Registry System: L-Proline, 3-hydroxy-5-methyl-, (3R,5R)- (9CI)(114717-06-5)

Safety Data

• Hazardous Substances Data: 114717-06-5(Hazardous Substances Data)

Upstream product

• 114681-13-9 (R)-3-Hydroxy-5-methyl-pyrrolidine-2-carboxylic acid methyl ester 
• 114658-41-2 (S)-Benzyloxycarbonylamino-((R)-3-methyl-4,5-dihydro-isoxazol-5-yl)-acetic acid methyl ester 
• 114658-43-4 (2S,3R)-2-Benzyloxycarbonylamino-3-hydroxy-5-oxo-hexanoic acid methyl ester 
• 114658-45-6 (R)-3-Hydroxy-5-methyl-3,4-dihydro-2H-pyrrole-2-carboxylic acid methyl ester 
• 213699-35-5 (3R,5R)-3-benzoyloxy-1-(tert-butoxycarbonyl)-5-methyl-2-pyrrolidinone 
• 213699-37-7 (3R,5R)-3-benzoyloxy-1-methoxycarbonyl-5-methyl-2-pyrrolidinone 
• 213699-26-4 (3R,5R)-3-(tert-Butyl-dimethyl-silanyloxy)-5-methyl-2-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 132945-96-1 tert-butyl (2R,4R)-4-{[tert-butyl(dimethyl)silyl]oxy}-2-methylpyrrolidine-1-carboxylate 
• 213699-36-6 (3R,5R)-3-benzoyloxy-5-methyl-2-pyrrolidinone 
• 213699-31-1 (3R,5R)-1-(tert-butoxycarbonyl)-3-hydroxy-5-methyl-2-pyrrolidinone 
• 213699-40-2 (2S,3R,5R)-3-benzoyloxy-2-cyano-1-methoxycarbonyl-5-methylpyrrolidine 

Relevant articles and documents

Diastereoselective syntheses of (2R,3R,5R)- and (2S,3S,5S)-3-hydroxy-5- methyl-2-pyrrolidinecarboxylic acid as a component of actinomycin Z1

A novel diastereoselective syntheses of both (2R,3R,5R)-1 and its enantiomer (2S,3S,5S)-1 were accomplished by employing trans-selective nucleophilic addition of cyanide to 3-benzoyloxy-N-acyliminium ions as the key step, starting from trans-4-hydroxy-L-p

Synthesis of (2S,3S,5S)-3-Hydroxy-5-methyl-2-pyrrolidinecarboxylic Acid, a Component of Actinomycin Z1

(2S,3S,5S)-3-Hydroxy-5-methyl-2-pyrrolidinecarboxylic acid and the enantiomer, the relative configurations of which are the same as that of the natural compound found in actinomycin Z1 were synthesized and the optical properties were determined