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35836-41-0

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35836-41-0 Usage

Description

(2,3-dihydroxy-4-methoxyphenyl)(phenyl)methanone, also known as dihydroxyacetophenone, is a chemical compound with the molecular formula C14H12O4. It is a ketone derivative with two hydroxyl groups and a methoxy group attached to a benzene ring. (2,3-dihydroxy-4-methoxyphenyl)(phenyl)methanone has been found in various plant species and is known for its antioxidant and anti-inflammatory properties. Its beneficial effects on skin health and aging have garnered interest in its potential use in pharmaceuticals and cosmetic products. Furthermore, it plays a role in the biosynthesis of secondary metabolites in certain plant species.

Uses

Used in Pharmaceutical Industry:
(2,3-dihydroxy-4-methoxyphenyl)(phenyl)methanone is used as a pharmaceutical agent for its antioxidant and anti-inflammatory properties. These characteristics make it a promising candidate for the development of treatments targeting various health conditions that can benefit from these effects.
Used in Cosmetic Products:
In the cosmetic industry, (2,3-dihydroxy-4-methoxyphenyl)(phenyl)methanone is used as an active ingredient for its positive impact on skin health and aging. Its presence in formulations can contribute to improved skin appearance, reduced signs of aging, and enhanced skin protection due to its antioxidant properties.
Used in Plant Metabolism Research:
(2,3-dihydroxy-4-methoxyphenyl)(phenyl)methanone is also used in scientific research as it is implicated in the biosynthesis of secondary metabolites in certain plant species. This makes it a valuable compound for studying plant metabolism and the production of bioactive compounds with potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 35836-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,3 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 35836-41:
(7*3)+(6*5)+(5*8)+(4*3)+(3*6)+(2*4)+(1*1)=130
130 % 10 = 0
So 35836-41-0 is a valid CAS Registry Number.

35836-41-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,3-dihydroxy-4-methoxyphenyl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names 2,3-dihydroxy-4-methoxy-benzophenone

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:35836-41-0 SDS

35836-41-0Downstream Products

35836-41-0Relevant articles and documents

Determination of the sequential order of acidity in a polyhydroxylated benzophenone series. Consequence on the oxidation reaction in relation to hepatotoxicity

Largeron, Martine,Langevin-Bermond, Dominique,Fleury, Maurice-Bernard

, p. 893 - 900 (2007/10/03)

The pKa values of successive acid-base equilibria involved in the pyrogallol ring ionisation of exifone, 2,3,4-trihydroxybenzophenone 1, and related methoxy derivatives were determined by UV-VIS absorption spectrometry and potentiometric titration.Due to strong intramolecular hydrogen bonding, the sequential order of acidity of the three hydroxy groups of 1 was found to be 4-OH > 3-OH > 2-OH.The polyhydroxylated benzophenones were oxidized to 3,4-quinone only in a narrow range of acidity in which the monoanionic 4-olate species predominated in solution.The attachment of an amino-alcohol residue resulted in the trapping of the transient 3,4-quinone and provided a convenient route to novel 1,4-benzoxazine derivatives.Cytotoxicity experiments in rat hepatocytes indicated that some of these compounds were significantly less toxic than the parent exifone.

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