173724-95-3 Usage
Description
(1S,3S)-phenylethylpyrrolidinylMethanol is a chiral organic compound with a molecular formula of C13H19NO. It contains an alcohol group and a pyrrolidine ring and is a derivative of phenylethylamine, a neurotransmitter and natural component of the human brain. Its chiral nature makes it important in the field of asymmetric synthesis and drug development.
Uses
Used in Pharmaceutical Industry:
(1S,3S)-phenylethylpyrrolidinylMethanol is used as a potential candidate for the development of pharmaceuticals targeting the central nervous system due to its derivative nature of phenylethylamine, a neurotransmitter in the human brain.
Used in Medicinal Chemistry:
(1S,3S)-phenylethylpyrrolidinylMethanol is used as a compound with potential applications in medicinal chemistry, particularly for the development of drugs targeting the central nervous system.
Used in Asymmetric Synthesis:
(1S,3S)-phenylethylpyrrolidinylMethanol is used as a chiral compound in the field of asymmetric synthesis, which is important for drug development as different enantiomers of chiral drugs can have vastly different effects in the body.
Used in Drug Development:
(1S,3S)-phenylethylpyrrolidinylMethanol is used as a compound with potential for further research and development in the pharmaceutical industry, particularly for the development of drugs targeting the central nervous system.
Check Digit Verification of cas no
The CAS Registry Mumber 173724-95-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,7,2 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 173724-95:
(8*1)+(7*7)+(6*3)+(5*7)+(4*2)+(3*4)+(2*9)+(1*5)=153
153 % 10 = 3
So 173724-95-3 is a valid CAS Registry Number.
173724-95-3Relevant articles and documents
Preparation method of chiral 3-substituted pyrrolidine derivative
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Paragraph 0064-0067, (2020/11/01)
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
Walker, Daniel P.,Acker, Brad A.,Jacobsen, E. Jon,Wishka, Donn G.
, p. 247 - 257 (2008/09/18)
(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
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Page/Page column 88; 89; 122, (2010/02/12)
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.
