90290-04-3

Basic information

• Product Name: trans-N-benzyl-2,5-bis(ethoxycarbonyl)pyrrolidine
• CAS NO: 90290-04-3
• Molecular Weight: 305.374
• Mol File: 90290-04-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: trans-N-benzyl-2,5-bis(ethoxycarbonyl)pyrrolidine(CAS DataBase Reference)
• NIST Chemistry Reference: trans-N-benzyl-2,5-bis(ethoxycarbonyl)pyrrolidine(90290-04-3)
• EPA Substance Registry System: trans-N-benzyl-2,5-bis(ethoxycarbonyl)pyrrolidine(90290-04-3)

Safety Data

• Hazardous Substances Data: 90290-04-3(Hazardous Substances Data)

Upstream product

• 17740-40-8 diethyl meso-1-benzyl-2,5-pyrrolidinedicarboxylate 
• 52321-06-9 cis-1-benzylpyrrolidine-2,5-dicarboxylic acid diethyl ester 
• 869-10-3 diethyl 2,5-dibromoadipate 
• 100-46-9 benzylamine 

Downstream Products

• 52321-06-9 cis-1-benzylpyrrolidine-2,5-dicarboxylic acid diethyl ester 
• 93713-33-8 rac-trans-1-Benzyl-2,5-dicarboxypyrrolidine 
• 52321-07-0 (2S,5S)-1-Benzylpyrrolidine-2,5-dicarboxylic acid 
• 90290-05-4 (2S,5S)-2,5-bis(methoxymethyl)pyrrolidine 
• 118396-01-3 (-)-(2S,5S)-N-benzyl-trans-2,5-bis(methoxycarbonyl)pyrrolidine 
• 120980-88-3 trans-1-(tert-Butoxycarboxyl)-2(S)-(methoxycarbonyl)-5(S)-<(tosyloxy)methyl>pyrrolidine 
• 136235-07-9 Racemic trans-1-(tert-Butoxycarbonyl)-2-(methoxycarbonyl)-5-<(tosyloxy)methyl>pyrrolidine 
• 136175-17-2 (2S,5S)-5-[(3S,5S)-1-Acetyl-5-(4-nitro-phenoxycarbonyl)-pyrrolidin-3-ylsulfanylmethyl]-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester 
• 136175-17-2 (2S,5S)-5-[(3S,5S)-1-Acetyl-5-(4-nitro-phenoxycarbonyl)-pyrrolidin-3-ylsulfanylmethyl]-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester 
• 90290-34-9 (R)-1-((2S,5S)-2,5-Bis-methoxymethoxymethyl-pyrrolidin-1-yl)-2-methyl-3-phenyl-propan-1-one 
• 90290-30-5 1-((2S,5S)-2,5-Bis-methoxymethoxymethyl-pyrrolidin-1-yl)-3-phenyl-propan-1-one 
• 93713-34-9 (2R,5R)-1-Benzyl-pyrrolidine-2,5-dicarboxylic acid; compound with 2-amino-1-(4-nitro-phenyl)-propane-1,3-diol 

Relevant articles and documents

Synthesis of bridged bicyclic amino alcohols as compact modules for medicinal chemistry

The efficient synthetic routes of three bridged bicyclic amino alcohols were reported. It is conceivable that these compounds could be readily used as compact modules in medicinal chemistry to fine-tune physicochemical and pharmacokinetic properties, in order to eventually improve the overall quality of small molecule drug candidates.