66162-38-7 Usage
Description
Pyrrolidine, 2-[(4-methoxyphenyl)methyl]is a chemical compound characterized by a pyrrolidine ring and a 4-methoxyphenylmethyl group. It is widely utilized in organic synthesis and medicinal chemistry as a fundamental building block for the creation of diverse pharmaceuticals and bioactive compounds.
Uses
Used in Pharmaceutical Industry:
Pyrrolidine, 2-[(4-methoxyphenyl)methyl]is employed as a key intermediate in the synthesis of various drugs, contributing to the development of therapeutic agents for a range of health conditions.
Used in Medicinal Chemistry:
Pyrrolidine, 2-[(4-methoxyphenyl)methyl]serves as a crucial component in medicinal chemistry, aiding in the design and synthesis of novel bioactive molecules with potential applications in treating central nervous system disorders, cancer, and infectious diseases.
It is imperative to exercise proper safety measures when handling Pyrrolidine, 2-[(4-methoxyphenyl)methyl]-, due to its potential health and environmental hazards if mismanaged.
Check Digit Verification of cas no
The CAS Registry Mumber 66162-38-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,1,6 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 66162-38:
(7*6)+(6*6)+(5*1)+(4*6)+(3*2)+(2*3)+(1*8)=127
127 % 10 = 7
So 66162-38-7 is a valid CAS Registry Number.
66162-38-7Relevant articles and documents
Construction of azacycles by intramolecular amination of organoboronates and organobis(boronates)
Xu, Peilin,Zhang, Mingkai,Ingoglia, Bryan,Allais, Christophe,Dechert-Schmitt, Anne-Marie R.,Singer, Robert A.,Morken, James P.
, p. 3379 - 3383 (2021/05/10)
Intramolecular amination of organoboronates occurs with a 1,2-metalate shift of an aminoboron ate complex to form azetidines, pyrrolidines, and piperidines. Bis(boronates) undergo site-selective amination to form boronate-containing azacycles. Enantiomerically enriched azacycles are formed with high stereospecificity.
Spasmolytic agents. I. Aminoalcohol esters having a phenethylamine-like moiety
Kanao,Hashizume,Ichikawa,Irie,Satoh,Isoda
, p. 180 - 188 (2007/10/02)
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