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2,5-dihydroxy-3,4-dimethoxy-benzoic acid is a naturally occurring organic compound with the molecular formula C9H10O6. It is a derivative of benzoic acid, featuring two hydroxyl groups at the 2nd and 5th carbon positions, and two methoxy groups at the 3rd and 4th carbon positions. 2,5-dihydroxy-3,4-dimethoxy-benzoic acid is known for its antioxidant properties and is found in various plants, including the leaves of the Rhus succedanea tree. It has been studied for its potential health benefits, such as anti-inflammatory and anticancer activities. The compound's structure endows it with unique chemical properties, making it a subject of interest in the field of natural products chemistry and pharmacology.

5653-45-2

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5653-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5653-45-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,5 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5653-45:
(6*5)+(5*6)+(4*5)+(3*3)+(2*4)+(1*5)=102
102 % 10 = 2
So 5653-45-2 is a valid CAS Registry Number.

5653-45-2SDS

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 2,5-dihydroxy-3,4-dimethoxy-benzoic acid

1.2 Other means of identification

Product number -
Other names 2,5-Dihydroxy-3,4-dimethoxy-benzoesaeure

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

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More Details:5653-45-2 SDS

5653-45-2Relevant articles and documents

Structure-activity relationship studies on UK-2A, a novel antifungal antibiotic from Streptomyces sp. 517-02. Part 5: Roles of the 9-membered dilactone-ring moiety in respiratory inhibition

Usuki, Yoshinosuke,Adachi, Noriko,Fujita, Ken-Ichi,Ichimura, Akio,Iio, Hideo,Taniguchi, Makoto

, p. 3319 - 3322 (2007/10/03)

Several open-chained analogues of UK-2A, a novel antifungal antibiotic isolated from Streptomyces sp. 517-02, were prepared for structure-activity studies. The in vitro antifungal activities of these compounds against Rhodotorula mucilaginosa IFO 0001 and the inhibition of uncoupler-stimulated respiration in bovine heart submitochondrial particles (SMP) were evaluated. Oxidative potentials were measured by cyclic voltammetry. An analogue prepared from dihexyl l-glutamate showed comparable inhibitory activity as UK-2A.

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