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4957-16-8

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4957-16-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4957-16-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,5 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4957-16:
(6*4)+(5*9)+(4*5)+(3*7)+(2*1)+(1*6)=118
118 % 10 = 8
So 4957-16-8 is a valid CAS Registry Number.

4957-16-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,4-trimethyl-5-[(2,4,5-trimethylphenyl)methyl]benzene

1.2 Other means of identification

Product number -
Other names Dipseudocumylmethane

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:4957-16-8 SDS

4957-16-8Downstream Products

4957-16-8Relevant articles and documents

-

Hendrickson,Wadsworth

, p. 877 (1958)

-

An efficient synthesis of diarylmethanes via InCl3*4H2O-catalyzed dehydration of electron-rich arenes with trioxane

Sun, Hong-Bin,Hua, Ruimao,Yin, Yingwu

, p. 2291 - 2294 (2007/10/03)

A facile, efficient and environmentally benign procedure for the synthesis of diarylmethanes via the reaction of arenes with trioxane catalyzed by InCl3*4H2O was developed. The reactions of aromatic compounds bearing electron-donating group proceeded smoothly affording the corresponding diarylmethanes in good to excellent yields.

SYNTHESIS OF SUBSTITUTED 2,4,5-TRIMETHYLDIPHENYLMETHANES

Pozdnyakovich, Yu. V.,Borodovitsyn, V. V.,Pozdnyakovich, S. A.,Shein, S. M.

, p. 353 - 359 (2007/10/02)

2,5-Dimethyldiphenylmethane and its 2'- and 4'-methyl, chloro, and nitro derivatives were obtained by the reaction of substituted benzyl chlorides with p-xylene in the presence of ferric chloride and zinc stearate.The yields of the 2,5-dimethyldiphenylmethanes depend on the nature of the substituent in the benzyl chloride and decrease with the substituents in the order NO2>Cl>H>CH3.The 2' and 4'-methyl, chloro, and aminoderivatives of 2,4,5-trimethyldiphenylmethane were synthesized by chloromethylation of the obtained diphenylmethanes with paraform in acetic acid in the presence of zinc chloride followed by reduction of the 2,5-dimethyl-4-chloromethyldiphenylmethanes with zinc in acetic acid.

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