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3112-79-6

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3112-79-6 Usage

Structure

Benzene ring with three methyl groups at positions 1, 3, and 5
Sulfonyl group attached to the 2-(2,4,6-trimethylphenyl) substituent

Physical state

White crystalline solid

Solubility

Insoluble in water
Soluble in organic solvents

Applications

Reagent in organic synthesis
Production of pharmaceuticals and agrochemicals

Additional properties

Antioxidant properties
Potential applications in the food industry
Stabilizer in polymers

Check Digit Verification of cas no

The CAS Registry Mumber 3112-79-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,1 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3112-79:
(6*3)+(5*1)+(4*1)+(3*2)+(2*7)+(1*9)=56
56 % 10 = 6
So 3112-79-6 is a valid CAS Registry Number.

3112-79-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-trimethyl-2-(2,4,6-trimethylphenyl)sulfonylbenzene

1.2 Other means of identification

Product number -
Other names 2.4.6.2'.4'.6'-Hexamethyl-diphenylsulfon

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:3112-79-6 SDS

3112-79-6Relevant articles and documents

Conformational studies by dynamic NMR. 80. Cog-wheel effect in the stereolabile helical enantiomers of dimesityl sulfoxide and sulfone

Casarini,Grilli,Lunazzi,Mazzanti

, p. 2757 - 2763 (2001)

The 1H NMR solution spectra of the title compounds display anisochronous lines for the o-methyl substituents below -170 °C, due to the existence of two propeller-like M and P conformational enantiomers. The free energies of activation for the i

Novel Sulfonylation reagent: Sulfuric Acid-Hexafluoroacetic Anhydride

Tyobeka, Themba E.,Hancock, Richard A.,Weigel, Helmut

, p. 114 - 115 (2007/10/02)

A mixture of sulfuric acid and hexafluoroacetic anhydride is an efficient reagent for the sulfonylation of aromatic compounds.

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