195727-70-9

Basic information

• Product Name: 1-Benzoyl-2-methoxy-5-(methoxycarbonyl)pyrrolidine
• Synonyms: 1-Benzoyl-2-methoxy-5-(methoxycarbonyl)pyrrolidine
• CAS NO: 195727-70-9
• Molecular Weight: 263.293
• Mol File: 195727-70-9.mol

Chemical Properties

• CAS DataBase Reference: 1-Benzoyl-2-methoxy-5-(methoxycarbonyl)pyrrolidine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Benzoyl-2-methoxy-5-(methoxycarbonyl)pyrrolidine(195727-70-9)
• EPA Substance Registry System: 1-Benzoyl-2-methoxy-5-(methoxycarbonyl)pyrrolidine(195727-70-9)

Safety Data

• Hazardous Substances Data: 195727-70-9(Hazardous Substances Data)

Upstream product

• 2577-48-2 methyl (2S)-pyrrolidine carboxylate 
• 147-85-3 L-proline 
• 98-88-4 benzoyl chloride 
• 5874-58-8 N-(benzoyl)-L-proline 
• 67-56-1 methanol 
• 5493-38-9 N-benzoyl-L-proline methyl ester 

Downstream Products

• 1338382-31-2 diethyl [(5R)-N-benzoyl-(2S)-methoxycarbonylpyrrolidin-5-yl]phosphonate 
• 1346907-17-2 diethyl [N-benzoyl-(2S)-methoxycarbonylpyrrolidin-5-yl]phosphonate 
• 1338382-30-1 dimethyl [(5R)-N-benzoyl-(2S)-methoxycarbonylpyrrolidin-5-yl]phosphonate 
• 1346907-22-9 C₁₉H₃₁NO₇P₂ 
• 1346907-19-4 diisopropyl ((2R)-N-benzoylpyrrolidin-2-yl)phosphonate 
• 1346907-02-5 di-n-butyl [(5R)-N-benzoyl-(2S)-methoxycarbonylpyrrolidin-5-yl]phosphonate 
• 1338382-33-4 diisopropyl [(5R)-N-benzoyl-(2S)-methoxycarbonylpyrrolidin-5-yl]phosphonate 
• 1338382-32-3 diphenyl [(5R)-N-benzoyl-(2S)-methoxycarbonylpyrrolidin-5-yl]phosphonate 
• 195727-73-2 ((2S,5R)-1-Benzyl-5-propyl-pyrrolidin-2-yl)-methanol 
• 195727-74-3 (3R,6R)-1-Benzyl-6-propyl-piperidin-3-ol 
• 2717-75-1 N-benzoyl-L-tryptophan methyl ester 

Relevant articles and documents

Synthesis of (-)-Pseudoconhydrine through Ring Enlargement of a L-Proline Derivative

A short synthesis of (-)-pseudoconhydrine is described from L-proline by using a ring enlargement reaction.

Electroorganic Chemistry. 81. Anodic Oxidation of Sulfonamides and Amidophosphates

Oxidation peak potentials of sulfonamides and amidophosphates were measured in acetonitrile and compared with the corresponding amides and carbamates.The results showed that the order of easiness of oxidation was amides > carbamates > amidophosphates > sulfonamides.Furthermore, the reaction of silyl enol ethers or trimethyl phosphite with anodically α-methoxylated sulfonamides or amidophosphates has clearly shown that the α-methoxylated compounds are useful starting materials in organic synthesis.For example, optically active L-tryptophan was synthesized from α-methoxylated N-(p-tolylsulfonyl)-L-proline ester.