142841-60-9

Basic information

• Product Name: 1-Pyrrolidinecarboxylic acid, 2-butyl-5-(4-hydroxyheptyl)-, phenylmethyl ester
• CAS NO: 142841-60-9
• Molecular Formula: C23H37NO3
• Molecular Weight: 375.552
• Mol File: 142841-60-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-Pyrrolidinecarboxylic acid, 2-butyl-5-(4-hydroxyheptyl)-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Pyrrolidinecarboxylic acid, 2-butyl-5-(4-hydroxyheptyl)-, phenylmethyl ester(142841-60-9)
• EPA Substance Registry System: 1-Pyrrolidinecarboxylic acid, 2-butyl-5-(4-hydroxyheptyl)-, phenylmethyl ester(142841-60-9)

Safety Data

• Hazardous Substances Data: 142841-60-9(Hazardous Substances Data)

Usage

Chemical class

Alpha amino acid esters This compound belongs to a class of organic compounds that are derived from alpha amino acids by esterification.

Ester derivative

Pyrrolidinecarboxylic acid, 2-butyl-5-(4-hydroxyheptyl), and phenylmethyl The compound is formed by the esterification of pyrrolidinecarboxylic acid with 2-butyl-5-(4-hydroxyheptyl) and phenylmethyl groups.

Potential pharmaceutical applications

Biological activity The compound has potential biological activity, making it a candidate for further research and development in the creation of new drugs.

Industrial applications

Production of cosmetics or fragrances Due to its unique structure and properties, the compound may have potential uses in the production of cosmetics and fragrances.

Structure

A combination of pyrrolidine, butyl, hydroxyheptyl, and phenylmethyl groups The compound's structure consists of a pyrrolidine ring, a butyl chain, a hydroxyheptyl group, and a phenylmethyl ester group, which contribute to its unique properties and potential applications.

Upstream product

• 927-77-5 n-propylmagnesium bromide 
• 142841-56-3 (2R,5R)-N-<(benzyloxy)carbonyl>-5-butyl-2-(4-oxobutyl)pyrrolidine 
• 142925-67-5 (2S,5S)-N-<(benzyloxy)carbonyl>-5-butyl-2-(4-oxobutyl)pyrrolidine 
• 54313-25-6 4-penten-1-yllithium 
• 142925-66-4 (2S,5S)-N-<(benzyloxy)carbonyl>-5-butyl-2-(4-hydroxybutyl)pyrrolidine 
• 142841-63-2 (5R,8R)-1,12-bis(benzoyloxy)-5,8-bis<(tert-butyldimethylsilyl)oxy>-1-dodecanol 
• 142841-70-1 (2S,5S)-N-<(benzyloxy)carbonyl>-2-<4-(benzoyloxy)butyl>-5-butylpyrrolidine 
• 142841-67-6 (5R,8R)-1-(benzoyloxy)-5,8-dodecanediol cyclic sulfate 
• 142841-66-5 (5R,8R)-1-(benzoyloxy)-5,8-dodecanediol 
• 142841-69-8 (2S,5S)-2-<4-(benzoyloxy)butyl>-5-butylpyrrolidine 
• 131618-30-9 (5R,8R)-5,8-Bis<(tert-butyldimethylsilyl)oxy>-1,12-dodecanediol 
• 142841-55-2 (2R,5R)-N-<(benzyloxy)carbonyl>-5-butyl-2-(4-hydroxybutyl)pyrrolidine 
• 142841-52-9 (2R,5R)-5-<4-(benzyloxy)butyl>-N-<(benzyloxy)carbonyl>-2-<4-(p-toluenesulfonyloxy)butyl>pyrrolidine 
• 142841-53-0 (2R,5R)-N-<(benzyloxy)carbonyl>-2-<4-(benzoyloxy)butyl>-5-butylpyrrolidine 

Downstream Products

• 943979-38-2 (3R,5S,8aR)-3-butyl-5-propyloctahydroindolidine 
• 67217-85-0 (-)-indolizidine 223AB 
• 142841-61-0 (2R,5R)-N-<(benzyloxy)carbonyl>-5-butyl-2-(4-oxoheptyl)pyrrolidine 

Relevant articles and documents

Synthesis of indolizidines (-)-195B, (-)-223AB and (-)-239AB: (2S,5R)- l-[(benzyloxy)carbonyl]-2-methoxycarbonyl-5-(4pentenyl)pyrrolidine as a versatile chiral building block

The total syntheses of three levogyre 3,5-disubstituted indolizidines, (-)-195B, (-)-223AB and (-)-239AB are described. The employed strategy is based on the utilization of the common enantiopure trans 2,5-disubstituted pyrrolidine 3, which is assembled b