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51837-72-0

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51837-72-0 Usage

Molecular structure

2-(2,5-dimethoxy-4-methylbenzoyl)-3-methoxybenzoic acid is a derivative of benzoic acid with a molecular formula of C17H17O5.

Functional groups

Contains both methoxy and methyl groups.

Biological properties

Has shown anti-inflammatory and potential anti-cancer properties in studies.

Pharmaceutical applications

It is a promising target for drug development.

Research and development

Its molecular structure suggests that it may have specific interactions with biological targets, making it a valuable chemical for further research and development in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 51837-72-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,8,3 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51837-72:
(7*5)+(6*1)+(5*8)+(4*3)+(3*7)+(2*7)+(1*2)=130
130 % 10 = 0
So 51837-72-0 is a valid CAS Registry Number.

51837-72-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,5-dimethoxy-4-methylbenzoyl)-3-methoxybenzoic 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:51837-72-0 SDS

51837-72-0Relevant articles and documents

A VERSATILE SYNTHESIS OF HYDROXY-9,10-ANTHRAQUINONE-2-CARBOXYLIC ACIDS

Smith, Colin W.,Ambler, Samantha J.,Steggles, David J.

, p. 7447 - 7450 (2007/10/02)

Islandicin, a mould metabolite, can be synthesised in a few, robust, high yielding steps.This procedure can be further elaborated to give a variety of hydroxy-9,10-anthraquinone-2-carboxylic acids.

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