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63458-90-2

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63458-90-2 Usage

Chemical composition

A salt formed by the combination of 1-methylimidazole and p-toluenesulfonic acid.

Solvent

Used as a solvent in various chemical reactions and processes.

Catalyst

Acts as a catalyst in numerous chemical reactions.

Ionic liquid

Utilized for its low volatility, non-flammability, and recyclability, making it a potential candidate for green chemistry applications.

Organic synthesis

Facilitates a wide range of organic synthesis processes.

Electrochemistry

Applied in electrochemical reactions and studies.

Material science

Contributes to the development and characterization of new materials.

High thermal stability

Capable of withstanding high temperatures without decomposing or losing its properties.

Solubility

Readily dissolves in various organic solvents, enhancing its utility in different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 63458-90-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,4,5 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63458-90:
(7*6)+(6*3)+(5*4)+(4*5)+(3*8)+(2*9)+(1*0)=142
142 % 10 = 2
So 63458-90-2 is a valid CAS Registry Number.

63458-90-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-METHYLIMIDAZOLIUM P-TOLUENESULFONATE

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:63458-90-2 SDS

63458-90-2Downstream Products

63458-90-2Relevant articles and documents

Solid supported type ion liquid catalytic synthesis of stearic acid pentaerythritol ester of method

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Paragraph 0022-0023, (2019/07/04)

The present invention discloses a solid supported ionic liquid catalytic synthesis of stearic acid pentaerythritol ester of method, characterized in that in order to stearic acid and pentaerythritol as the raw materials, to solid supported type imidazole ion liquid as the use of the catalyst. The invention adopts the sol-gel process solid-ionic liquid, the catalyst amount is alcohol, acid always mole number of 1% - 5%, the reaction temperature is at 110 - 170 °C, normal pressure, reaction time 1 - 5 h; the characteristic of this invention is not adopted the pollution to the environment of the concentrated sulfuric acid, with the traditional inorganic acid as compared with the catalyst, solid-ionic liquid has high catalyst activity, mild reaction, esterification rate high, obtained by the production process is simplified, catalyst recovery simple operation and the like.

A triflate hydrodeoxygenation route to resveratrol from syringaldehyde

Davis, Matthew C.,Parrish, Damon A.,Harvey, Benjamin G.

, p. 304 - 313 (2013/07/26)

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Tunable protic ionic liquids as solvent-catalysts for improved synthesis of multiply substituted 1,2,4-triazoles from oxadiazoles and organoamines

Chen, Xiaofeng,Liu, Rui,Xu, Yuan,Zou, Gang

body text, p. 4813 - 4819 (2012/07/31)

More than green alternatives to traditional volatile molecular organic solvents, protic ionic liquids as dual solvent-catalysts have been successfully used to promote reactions of organoamines with oxadiazoles to afford sterically hindered 1,2,4-triazoles. Among the tested protic ionic liquids, pyridinium trifluoroacetate and acetate showed the highest efficiency for the reactions of arylamines and alkylamines, respectively, indicating that tunable catalysis could be readily effected with protic ionic liquid solvent-catalysts by simply tuning their cation and anion counterparts. A general and efficient approach has been developed for synthesis of multiply substituted 1,2,4-triazoles based on the tunable protic ionic liquid solvent-catalyst systems.

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