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Thiazolium, 3-ethyl-2-methyl-4-phenyl-, iodide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24840-73-1

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24840-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24840-73-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,8,4 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24840-73:
(7*2)+(6*4)+(5*8)+(4*4)+(3*0)+(2*7)+(1*3)=111
111 % 10 = 1
So 24840-73-1 is a valid CAS Registry Number.

24840-73-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethyl-2-methyl-4-phenyl-1,3-thiazol-3-ium,iodide

1.2 Other means of identification

Product number -
Other names 3-Aethyl-2-methyl-4-phenyl-thiazolium,Jodid

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:24840-73-1 SDS

24840-73-1Relevant academic research and scientific papers

Substituent and Solvent Effects on the Rate of the Reaction of 2-Methyl-4-phenyl-thiazole Ethiodide with Substituted Benzaldehydes

Mahmoud, M. R.,El-Kashef, H. M. S.,El-Nady, A. M.

, p. 657 - 670 (2007/10/02)

Condensation of 2-methyl-4-phenyl-thiazole ethiodide (1) with aromatic aldehydes in presence of piperidine as base catalyst has been studied kinetically at different temperatures.The rate in presence of low concentration of piperidine ( .On the other hand the rate in presence of >/= 1.013 M piperidine is represented by the second-order equation: v=k' .It is concluded from the kinetic results that the dehydration step of the intermediate aldol compound is the rate determining step of the reaction.The dependence of the mechanism of the reaction and the thermodynamic parameters of activation on the molecular structure of the various aromatic aldehydes used is discussed.In various organic solvents, the rate of the reaction increases as the dielectric constant of the medium is increased.The energy of activation and the thermodynamic parameters of activation were calculated and discussed in terms of solvent properties. - Keywords: Reaction mechanism / Solvent effects / Substituent effects

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