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Quinoline, 4-methyl-2-[(4-methylphenyl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64789-02-2

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64789-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64789-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,8 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64789-02:
(7*6)+(6*4)+(5*7)+(4*8)+(3*9)+(2*0)+(1*2)=162
162 % 10 = 2
So 64789-02-2 is a valid CAS Registry Number.

64789-02-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-2-p-tolylsulfanyl-quinoline

1.2 Other means of identification

Product number -
Other names 4-METHYL-2-[(4-METHYLPHENYL)SULFANYL]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:64789-02-2 SDS

64789-02-2Downstream Products

64789-02-2Relevant academic research and scientific papers

Nickel-Catalyzed Thiolation of Aryl Halides and Heteroaryl Halides through Electrochemistry

Liu, Dong,Ma, Hong-Xing,Fang, Ping,Mei, Tian-Sheng

, p. 5033 - 5037 (2019)

Transition-metal-catalyzed coupling reactions are useful tools for synthesizing aryl sulfur compounds. However, conventional transition-metal-catalyzed thiolation of aryl bromides and chlorides typically requires the use of strong base under elevated reaction temperature. Herein, we report the first examples of nickel-catalyzed electrochemical thiolation of aryl bromides and chlorides in the absence of an external base at room temperature using undivided electrochemical cells.

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