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8-chloro-6-methyl-2-phenylquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22960-24-3

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22960-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22960-24-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,6 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 22960-24:
(7*2)+(6*2)+(5*9)+(4*6)+(3*0)+(2*2)+(1*4)=103
103 % 10 = 3
So 22960-24-3 is a valid CAS Registry Number.

22960-24-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-chloro-6-methyl-2-phenylquinoline

1.2 Other means of identification

Product number -
Other names 8-chloro-6-methyl-2-phenyl-quinoline

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:22960-24-3 SDS

22960-24-3Downstream Products

22960-24-3Relevant academic research and scientific papers

Facile synthesis of substituted quinolines by iron(iii)-catalyzed cascade reaction between anilines, aldehydes and nitroalkanes

Mahato, Sachinta,Mukherjee, Anindita,Santra, Sougata,Zyryanov, Grigory V.,Majee, Adinath

, p. 7907 - 7917 (2019)

A library of substituted quinolines has been synthesized by the reaction of aldehydes, anilines and nitroalkanes using a catalytic amount of Fe(iii) chloride. The reaction is a simple, efficient, one-pot, three-component domino strategy in ambient air which afforded the products in high yields. A probable pathway of the reaction is a sequential aza-Henry reaction/cyclization/denitration. The use of commercially available chemicals as starting materials, an inexpensive metal catalyst, aerobic reaction conditions, tolerance of a wide range of functional groups, and operational simplicity are the notable advantages of this present protocol.

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