926913-20-4

Basic information

• Product Name: 1-Pyrrolidinecarboxylic acid, 3-[bis(4-methoxyphenyl)phenylmethoxy]-4-[(methylsulfonyl)oxy]-, 1,1-dimethylethyl ester, (3S,4R)-
• CAS NO: 926913-20-4
• Molecular Formula: C31H37NO8S
• Molecular Weight: 583.703
• Mol File: 926913-20-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-Pyrrolidinecarboxylic acid, 3-[bis(4-methoxyphenyl)phenylmethoxy]-4-[(methylsulfonyl)oxy]-, 1,1-dimethylethyl ester, (3S,4R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Pyrrolidinecarboxylic acid, 3-[bis(4-methoxyphenyl)phenylmethoxy]-4-[(methylsulfonyl)oxy]-, 1,1-dimethylethyl ester, (3S,4R)-(926913-20-4)
• EPA Substance Registry System: 1-Pyrrolidinecarboxylic acid, 3-[bis(4-methoxyphenyl)phenylmethoxy]-4-[(methylsulfonyl)oxy]-, 1,1-dimethylethyl ester, (3S,4R)-(926913-20-4)

Safety Data

• Hazardous Substances Data: 926913-20-4(Hazardous Substances Data)

Upstream product

• 150986-62-2 S,S-3,4-dihydroxypyrrolidine-1-carboxylic acid tert-butyl ester 
• 24424-99-5 di-tert-butyl dicarbonate 
• 926913-15-7 (3R,4S)-1-N-tert-butyloxycarbonyl-3-(4,4'-dimethoxytrityloxy)-4-(4-nitrobenzoyloxy)-pyrrolidine 
• 926913-07-7 (3S,4S)-1-N-tert-butyloxycarbonyl-3-(4,4'-dimethoxytrityloxy)-4-hydroxypyrrolidine 
• 926913-17-9 (3S,4R)-1-N-tert-butyloxycarbonyl-3-(4,4'-dimethoxytrityloxy)-4-hydroxypyrrolidine 
• 124-63-0 methanesulfonyl chloride 

Downstream Products

• 190792-74-6 (3S,4S)-4-amino-1-N-tert-butyloxycarbonyl-3-hydroxypyrrolidine 
• 926913-27-1 (3S,4S)-4-(adenin-9-yl)-1-N-tert-butyloxycarbonyl-3-(4,4'-dimethoxytrityloxy)pyrrolidine 
• 926913-26-0 (3S,4S)-1-N-tert-butyloxycarbonyl-3-(4,4'-dimethoxytrityloxy)-4-(thymin-1-yl)-pyrrolidine 

Relevant articles and documents

Synthesis of diastereomeric 3-hydroxy-4-pyrrolidinyl derivatives of nucleobases

The work deals with the synthesis of hydroxypyrrolidine analogs of nucleosides. Starting from the optically pure l- or d-tartaric acid, we improved the synthesis of enantiomeric trans-3,4-dihydroxypyrrolidines and elaborated a procedure for the synthesis of all possible diastereoisomers of 3-hydroxy-4-pyrrolidinyl derivatives of both purine and pyrimidine nucleobases. The prepared compounds were tested for cytostatic and antiviral properties but no significant activity was found.