173724-95-3

Basic information

• Product Name: (1S,3S)-phenylethylpyrrolidinylMethanol
• Synonyms: (1S,3S)-phenylethylpyrrolidinylMethanol;3-Pyrrolidinemethanol, 1-[(1S)-1-phenylethyl]-, (3S)-;((S)-1-((S)-1-Phenylethyl)pyrrolidin-3-yl)methanol
• CAS NO: 173724-95-3
• Molecular Formula: C₁₃H₁₉NO
• Molecular Weight: 205.29606
• Product Categories: organic building block
• Mol File: 173724-95-3.mol
• Article Data: 13

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: (1S,3S)-phenylethylpyrrolidinylMethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,3S)-phenylethylpyrrolidinylMethanol(173724-95-3)
• EPA Substance Registry System: (1S,3S)-phenylethylpyrrolidinylMethanol(173724-95-3)

Safety Data

• Hazardous Substances Data: 173724-95-3(Hazardous Substances Data)

Usage

General Description

(1S,3S)-phenylethylpyrrolidinylMethanol is a chiral compound with a molecular formula of C13H19NO. It is an organic compound that contains an alcohol group and a pyrrolidine ring. It is a derivative of phenylethylamine, which is a neurotransmitter and a natural component of the human brain. The compound has potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting the central nervous system. Its chiral nature makes it important in the field of asymmetric synthesis and drug development, as different enantiomers of chiral drugs can have vastly different effects in the body. (1S,3S)-phenylethylpyrrolidinylMethanol has potential for further research and development in the pharmaceutical industry.

Upstream product

• 173340-19-7 (3S)-1-((S)-1-phenylethyl)-5-oxo-3-pyrrolidinecarboxylic acid 
• 146348-14-3 methyl 5-oxo-1-((S)-1-phenylethyl)pyrrolidine-3-(S)-carboxylate 
• 97-65-4 2-methylenesuccinic acid 
• 618-36-0 rac-methylbenzylamine 
• 2627-86-3 (S)-1-phenyl-ethylamine 

Downstream Products

• 508201-49-8 (3S)-1-[(S)-1-phenethyl]-3-(chloromethyl) pyrrolidine 
• 153566-63-3 (3R)-1-[(1S)-1-phenylethyl]-3-pyrrolidineacetonitrile 
• 174676-79-0 methyl (3R,1'S)-<1-(1'-phenyleth-1'-yl)-pyrrolidin-3-yl> acetate 
• 191348-04-6 (S)-3-formylpyrrolidine-1-carboxylic acid t-butyl ester 
• 199174-24-8 tert-butyl (3S)-3-(hydroxymethyl)pyrrolidine-1-carboxylate 
• 852655-80-2 2-[1-(1-phenyl-ethyl)-pyrrolidin-3-ylmethyl]-isoindole-1,3-dione 

Relevant articles and documents

Preparation method of chiral 3-substituted pyrrolidine derivative

The invention provides a preparation method of a chiral 3-substituted pyrrolidine derivative. The preparation method comprises an intermediate preparation step, a diastereomer mixture preparation step, a chiral separation step and a chiral 3-substituted pyrrolidine derivative synthesis step. According to the invention, through catalytic asymmetric kinetic resolution, a mixture of two diastereoisomers is efficiently converted into a diastereoisomer with a certain single configuration, chiral separation is realized, a key intermediate is obtained with high yield, and a series of chiral 3-substituted pyrrolidine derivatives are synthesized. The whole reaction route is mild in reaction condition, simple and convenient to operate, high in resolution efficiency, high in atom economy, low in costand suitable for industrial scale production.

Preparation of novel azabicyclic amines and α7 nicotinic acetylcholine receptor activity of derived aryl amides

(Chemical Equation Presented) Three new azabicyclic amines, namely exo-3-amino-1-azabicyclo[3.2.1]octane, 3-amino-1-azabicyclo-[3.2.2]nonane and exo-6-amino-8-azabicyclo[3.2.1]octane, have been designed and prepared as isosteres of 3-aminoquinuclidine. Ar

QUINOLONE ANTIBACTERIAL AGENTS

Compounds of formula (I) wherein A is formula (II), formula (III) or formula (IV), and B is formula (V), formula (VI), or formula (VII), can be used in a variety of applications including use as antibacterial agents.