1026537-24-5

Basic information

• Product Name: 4-(2-methoxy-phenyl)-2,3-dihydro-pyrrole-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester
• Synonyms: 4-(2-methoxy-phenyl)-2,3-dihydro-pyrrole-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester
• CAS NO: 1026537-24-5
• Molecular Weight: 333.384
• Mol File: 1026537-24-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-(2-methoxy-phenyl)-2,3-dihydro-pyrrole-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-methoxy-phenyl)-2,3-dihydro-pyrrole-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester(1026537-24-5)
• EPA Substance Registry System: 4-(2-methoxy-phenyl)-2,3-dihydro-pyrrole-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester(1026537-24-5)

Safety Data

• Hazardous Substances Data: 1026537-24-5(Hazardous Substances Data)

Upstream product

• 102195-80-2 (S)-1-tert-butyl 2-methyl 4-oxopyrrolidine-1,2-dicarboxylate 
• 74844-91-0 1-tert-butyl 2-methyl (2S,4R)-4-hydroxy-1,2-pyrrolidinedicarboxylate 
• 5720-06-9 2-Methoxyphenylboronic acid 
• 284047-10-5 1-tert-butyl 2-methyl (2S)-4-(trifluoromethanesulfonyloxy)-2,3-dihydropyrrole-1,2-dicarboxylate 

Downstream Products

• 1026165-83-2 C₂₉H₄₃N₃O₈S₃ 
• 1026151-32-5 C₃₀H₄₅N₃O₈S₃ 
• 1026079-77-5 (R)-4-{(E)-3-[(2S,4R)-2-((S)-1-Methoxycarbonyl-3-methylsulfanyl-propylcarbamoyl)-4-(2-methoxy-phenyl)-pyrrolidin-1-yl]-propenyl}-2,2-dimethyl-thiazolidine-3-carboxylic acid tert-butyl ester 
• 1026163-04-1 (2S,4R)-2-((S)-1-Methoxycarbonyl-3-methylsulfanyl-propylcarbamoyl)-4-(2-methoxy-phenyl)-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 1026917-85-0 (2S,4R)-4-(2-Methoxy-phenyl)-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 
• 1027555-83-4 (2S,4R)-4-(2-Methoxy-phenyl)-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester 

Relevant articles and documents

Synthesis and evaluation of some hydroxyproline-derived peptidomimetics as isoprenyltransferase inhibitors

CA1A2X peptidomimetics containing a modified proline at position A2 were prepared and evaluated for their ability to inhibit farnesyltransferase (FTase) and geranylgeranyltransferase I (GGTase I) in enzymatic and cell- bas