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Benzoic acid, 2-[(3-methylphenyl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84964-59-0

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84964-59-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84964-59-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,9,6 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84964-59:
(7*8)+(6*4)+(5*9)+(4*6)+(3*4)+(2*5)+(1*9)=180
180 % 10 = 0
So 84964-59-0 is a valid CAS Registry Number.

84964-59-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-methylphenyl)sulfanylbenzoic acid

1.2 Other means of identification

Product number -
Other names 2-carboxy-3'-methyldiphenyl sulfide

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:84964-59-0 SDS

84964-59-0Relevant academic research and scientific papers

Gas phase generation and cyclisation reactions of some o-substituted phenyl radicals

Cadogan,Hutchison,McNab

, p. 7747 - 7762 (2007/10/02)

Flash vacuum pyrolysis of the allyl esters 2 (X=O, S, CH2, CO) at 900°C (10-2 Torr) gives dibenzofurans, dibenzothiophenes, fluorenes, and fluorenones respectively as the major products. The mechanism involves the phenyl radical intermediates 1 which equilibrate by intramolecular hydrogen transfer via six-membered transition states, prior to cyclisation.

Methyl substituted thioxanthones and thioxanthone-10,10-dioxides

Brindle, Ian D.,Doyle, Paul P.

, p. 1869 - 1871 (2007/10/02)

The preparation of all four monomethylthioxanthones and their corresponding dioxides is described.A previously published synthesis of the 2- and 3-methylthioxanthones by Gilman and Diehl has been shown to produce the 2- and 4-methyl isomers.

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