351529-73-2

Basic information

• Product Name: (RS)-[(2S,4R)-1-benzyl-4-tert-butyldimethylsilyloxypyrrolidin-2-yl]-(1-methylpyrazol-5-yl)methanol
• Synonyms: (RS)-[(2S,4R)-1-benzyl-4-tert-butyldimethylsilyloxypyrrolidin-2-yl]-(1-methylpyrazol-5-yl)methanol
• CAS NO: 351529-73-2
• Molecular Weight: 401.624
• Mol File: 351529-73-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (RS)-[(2S,4R)-1-benzyl-4-tert-butyldimethylsilyloxypyrrolidin-2-yl]-(1-methylpyrazol-5-yl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (RS)-[(2S,4R)-1-benzyl-4-tert-butyldimethylsilyloxypyrrolidin-2-yl]-(1-methylpyrazol-5-yl)methanol(351529-73-2)
• EPA Substance Registry System: (RS)-[(2S,4R)-1-benzyl-4-tert-butyldimethylsilyloxypyrrolidin-2-yl]-(1-methylpyrazol-5-yl)methanol(351529-73-2)

Safety Data

• Hazardous Substances Data: 351529-73-2(Hazardous Substances Data)

Upstream product

• 930-36-9 1-methyl-1H-pyrazole 
• 156440-98-1 (2S,4R)-N-benzyl-4-(tert-butyldimethylsilyloxy)pyrrolidine-2-carbaldehyde 

Downstream Products

• 164161-74-4 (2R,4S)-2-(2-Methyl-2H-pyrazol-3-ylmethyl)-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid allyl ester 
• 164162-08-7 (2R,4S)-1-allyloxycarbonyl-4-benzylthio-2-[(4-hydroxymethyl-1-methylpyrazol-5-yl)methyl]pyrrolidine 
• 164162-04-3 (2R,4R)-1-benzyl-4-tert-butyldimethylsilyloxy-2-[(4-hydroxymethyl-1-methylpyrazol-5-yl)methyl]pyrrolidine 
• 156441-99-5 (2R,4S)-1-Allyloxycarbonyl-4-benzoylthio-2-(1-methylpyrazol-5-ylmethyl)-pyrrolidine 
• 164162-02-1 (2R,4R)-1-benzyl-2-[(4-bromo-1-methylpyrazol-5-yl)methyl]-4-tert-butyldimethylsilyloxypyrrolidine 
• 164162-03-2 (2R,4R)-1-benzyl-4-tert-butyldimethylsilyloxy-2-[(4-formyl-1-methylpyrazol-5-yl)methyl]pyrrolidine 
• 164162-01-0 (2R,4R)-1-benzyl-4-tert-butyldimethylsilyloxy-2-[(1-methylpyrazol-5-yl)methyl]pyrrolidine 

Relevant articles and documents

Synthesis and antibacterial activity of novel 4-pyrrolidinylthio carbapenems. Part IV. 2-Alkyl substituents containing cationic heteroaromatics linked via a C-C bond

The synthesis and biological activity of a novel series of 2-alkyl-4-pyrrolidinylthio-β-methylcarbapenems containing a variety of cationic heteroaromatic substituents linked via a C-C bond is described. As a result of these studies, we selected FR21818 (1

Substituted 3-pyrrolidinylthio-carbapenems as antimicrobial agents

A compound of the formula: STR1 in which R1 is carboxy or protected carboxy, R2 is 1-hydroxyethyl, R3 is methyl, R4 is optionally substituted pyridyl(lower)alkyl, optionally N-substituted 2-oxopiperazin-1-yl-(lo