385440-93-7

Basic information

• Product Name: 1-Pyrrolidinecarboxylic acid, 2-(hydroxymethyl)-4-[[(4-methylphenyl)sulfonyl]oxy]-, 1,1-dimethylethyl ester, (2S,4R)-
• CAS NO: 385440-93-7
• Molecular Formula: C17H25NO6S
• Molecular Weight: 371.455
• Mol File: 385440-93-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-Pyrrolidinecarboxylic acid, 2-(hydroxymethyl)-4-[[(4-methylphenyl)sulfonyl]oxy]-, 1,1-dimethylethyl ester, (2S,4R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Pyrrolidinecarboxylic acid, 2-(hydroxymethyl)-4-[[(4-methylphenyl)sulfonyl]oxy]-, 1,1-dimethylethyl ester, (2S,4R)-(385440-93-7)
• EPA Substance Registry System: 1-Pyrrolidinecarboxylic acid, 2-(hydroxymethyl)-4-[[(4-methylphenyl)sulfonyl]oxy]-, 1,1-dimethylethyl ester, (2S,4R)-(385440-93-7)

Safety Data

• Hazardous Substances Data: 385440-93-7(Hazardous Substances Data)

Upstream product

• 125653-58-9 (2S,4R)-2-(tert-butyldimethylsilanyloxymethyl)-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 98-59-9 p-toluenesulfonyl chloride 
• 51-35-4 4R-4-hydroxyproline 
• 40216-83-9 L-4-hydroxyproline methyl ester hydrochloride 
• 74844-91-0 1-tert-butyl 2-methyl (2S,4R)-4-hydroxy-1,2-pyrrolidinedicarboxylate 
• 88043-21-4 (2S,4R)-4-(toluene-4-sulfonyloxy)-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester 

Downstream Products

• 385440-71-1 (2S-trans)-2-[cyano[(phenylmethyl)amino]methyl]-4-[[(4-methylphenyl)-sulfonyl]oxy]-1-pyrrolidinecarboxylic acid, 1,1-dimethylethyl ester 
• 385440-70-0 (2S,4R)-2-Formyl-4-(toluene-4-sulfonyloxy)-pyrrolidine-1-carboxylic acid tert-butyl ester 

Relevant articles and documents

IMIDAZO[4,5-C]QUINOLINE COMPOUNDS AND THEIR USE AS ATM KINASE INHIBITORS

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The synthesis and evaluation of [2.2.1]-bicycloazahydantoins as androgen receptor antagonists

A novel series of [2.2.1]-bicycloazahydantoins has been designed and synthesized in an enantiospecific manner. Several of these compounds were found to act as antagonists to the androgen receptor. A novel series of [2.2.1]-azahydantoins has been designed

Selective androgen receptor modulators and methods for their identification, design and use

Selective androgen receptor modulators (SARMs) having antagonist activity in hormone-dependent tumors while exhibiting no activity or agonist activity against other nontumor tissues containing the androgen receptor as well as methods for identifying, designing and using SARMs are provided.