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105330-59-4

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105330-59-4 Usage

General Description

(2R,3S)-3,4-Dihydro-2-(3-hydroxy-4-methoxyphenyl)-5,7-dimethoxy-2H-1-benzopyran-3-ol, also known as dihydromorin, is a natural phenolic compound found in plants like Morus alba. It is a type of flavonoid, which is a group of polyphenolic compounds known for their antioxidant properties. Dihydromorin has been found to have a range of potential health benefits, including anti-inflammatory, anti-cancer, and cardioprotective effects. It has also been researched for its potential in treating diabetes and obesity. (2R,3S)-3,4-Dihydro-2-(3-hydroxy-4-methoxyphenyl)-5,7-dimethoxy-2H-1-benzopyran-3-ol is of interest to researchers seeking natural bioactive compounds for medicinal use, and it may hold promise for the development of new pharmaceuticals or supplements.

Check Digit Verification of cas no

The CAS Registry Mumber 105330-59-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,3,3 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 105330-59:
(8*1)+(7*0)+(6*5)+(5*3)+(4*3)+(3*0)+(2*5)+(1*9)=84
84 % 10 = 4
So 105330-59-4 is a valid CAS Registry Number.

105330-59-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,7,4'-Tri-O-methylcatechin

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:105330-59-4 SDS

105330-59-4Relevant articles and documents

An efficient synthesis of the four mono methylated isomers of (+)-catechin including the major metabolites and of some dimethylated and trimethylated analogues through selective protection of the catechol ring

Cren-Olive, Cecile,Lebrun, Stephane,Rolando, Christian

, p. 821 - 830 (2007/10/03)

The four monomethylated isomers of (+)-catechin in positions 3′, 4′, 5 and 7, two dimethylated derivatives, the 5,7-dimethylcatechin and the 3′, 4′-dimethylcatechin and two trimethylated isomers of (+)-catechin in positions 3′, 5, 7 and 4′, 5, 7 were synthesized by a new method based on successive and selective protections of the various phenol functions present on (+)-catechin. The key step was the selective protection of the catechol ring with dichlorodiphenylmethane and di-tert-butyldichlorosilane.

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