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66162-38-7

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66162-38-7 Usage

General Description

Pyrrolidine, 2-[(4-methoxyphenyl)methyl]- is a chemical compound with a pyrrolidine ring and a 4-methoxyphenylmethyl group attached. It is commonly used in organic synthesis and medicinal chemistry as a building block for the synthesis of various pharmaceuticals and bioactive compounds. This chemical has potential applications in the development of drugs for various therapeutic areas, including central nervous system disorders, cancer, and infectious diseases. It is important to handle and use this chemical with proper safety precautions, as it may pose health and environmental hazards if not handled properly.

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.

66162-38-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-methoxyphenyl)methyl]pyrrolidine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:66162-38-7 SDS

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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