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3-methoxy-2-{[(4-methylphenyl)sulfonyl]oxy}benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93945-52-9

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93945-52-9 Usage

Main properties and specific content

Derivative of benzoic acid
Contains a methoxy group and a sulfonyloxy group attached to the benzene ring
4-methylphenyl group linked to the sulfonyloxy group
Commonly used in pharmaceutical and medicinal applications

Potential therapeutic properties

anti-inflammatory, analgesic, and antioxidant effects
Valuable candidate for the development of new drugs for various medical conditions
Further studies and research are needed to fully understand and harness its potential for therapeutic purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 93945-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,4 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93945-52:
(7*9)+(6*3)+(5*9)+(4*4)+(3*5)+(2*5)+(1*2)=169
169 % 10 = 9
So 93945-52-9 is a valid CAS Registry Number.

93945-52-9SDS

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 3-methoxy-2-(4-methylphenyl)sulfonyloxybenzoic acid

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:93945-52-9 SDS

93945-52-9Relevant academic research and scientific papers

Concise approach to mono- And disubstituted luotonin A analogs and their cytotoxicity test

Kagawa, Natsuko,Nishimura, Kimiko,Abe, Shinya,Masuko, Takashi,Toyota, Masahiro

, p. 514 - 522 (2019/07/31)

A concise approach for the preparation of luotonin A analogs has been developed. The new synthetic route contains an anion-assisted intramolecular double hetero Diels Alder reaction and a direct oxidative cross coupling reaction. Some synthetic luotonin A analogs show cytotoxic activities against Daudi and Jurkat human cancer cells as potent as camptothecin.

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