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Benzenesulfonic acid, 3,5-dimethyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89762-87-8

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89762-87-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89762-87-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,6 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89762-87:
(7*8)+(6*9)+(5*7)+(4*6)+(3*2)+(2*8)+(1*7)=198
198 % 10 = 8
So 89762-87-8 is a valid CAS Registry Number.

89762-87-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3,5-dimethylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names Benzenesulfonic acid,3,5-dimethyl-,methyl ester

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:89762-87-8 SDS

89762-87-8Upstream product

89762-87-8Relevant academic research and scientific papers

Copper-Catalyzed Multicomponent Reaction of DABCO·(SO2)2, Alcohols, and Aryl Diazoniums for the Synthesis of Sulfonic Esters

Wang, Yang,Deng, Lingling,Deng, Yu,Han, Jianlin

, p. 4674 - 4680 (2018)

A Cu-catalyzed multicomponent cascade reaction of DABCO·(SO2)2 (DABSO), alcohol, and aryl diazonium tetrafluoroborate was developed which afforded sulfonic esters in moderate to good chemical yields. In this reaction, the SO2 surrogate DABSO was used for the first time in the synthesis of sulfonic aliphatic esters. This multicomponent reaction was carried out under mild conditions and tolerated a wide range of substrates, which provides a new and efficient strategy for the synthesis of sulfonic esters.

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