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

66234-36-4

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66234-36-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66234-36-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,3 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66234-36:
(7*6)+(6*6)+(5*2)+(4*3)+(3*4)+(2*3)+(1*6)=124
124 % 10 = 4
So 66234-36-4 is a valid CAS Registry Number.

66234-36-4SDS

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-(o,p-dimethylbenzyl)pyridine

1.2 Other means of identification

Product number -
Other names 2-(2,4-dimethyl-benzyl)-pyridine

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:66234-36-4 SDS

66234-36-4Downstream Products

66234-36-4Relevant academic research and scientific papers

SENSITIVE NATURE OF LIGAND COUPLING AND PSEUDOROTATION TO ELECTRONIC EFFECT OF SUBSTITUENT---LIGAND COUPLING IN THE REACTIONS OF BENZYLIC ARYL SULFOXIDES WITH BENZYLIC GRIGNARD REAGENTS

Wakabayashi, Shoji,Ishida, Masahiro,Takeda, Takashi,Oae, Shigeru

, p. 4441 - 4444 (2007/10/02)

Unlike the reaction of benzylic 2-pyridyl sulfoxides with benzylic Grignard reagents, in the reaction of p-benzenesulfonylphenyl benzylic sulfoxides with benzylic Grignard reagents, benzylic groups bearing an electronwithdrawing group tends to couple with the aryl group preferentially.This change is considered to be due to a slight change of electronic environements which would effect on the ease of pseudorotation of the incipient ?-sulfurane formed during the reaction.

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