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66568-98-7

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66568-98-7 Usage

Chemical compound

5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-2,3-dihydro-4H-chromen-4-one

Properties

Antioxidant and anti-inflammatory

Source

Found in various plants, including citrus fruits

Health benefits

Potential role in preventing and treating diseases such as cancer, cardiovascular disease, and neurodegenerative disorders

Mechanisms

Scavenges free radicals, reduces oxidative stress, inhibits production of inflammatory markers, modulates immune response

Check Digit Verification of cas no

The CAS Registry Mumber 66568-98-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,5,6 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 66568-98:
(7*6)+(6*6)+(5*5)+(4*6)+(3*8)+(2*9)+(1*8)=177
177 % 10 = 7
So 66568-98-7 is a valid CAS Registry Number.

66568-98-7SDS

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 5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one

1.2 Other means of identification

Product number -
Other names 2,3-dihydro-5-hydroxy-2-(4'-hydroxy-3'-methoxyphenyl)-7-methoxy-4H-1-benzopyran-4-one

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:66568-98-7 SDS

66568-98-7Relevant articles and documents

One step synthesis of polyhydroxyflavan ones from hydroxyacetophenones and hydroxybenzaldehydes

Chan, Wing Lai,Lin, Yong Cheng,Zhang, Wei Han,Tang, Pak Lai,Szeto, Yau Shan

, p. 551 - 554 (2007/10/03)

Polyhydroxyflavanones were synthesized in a one-step process by reacting the appropriate hydroxyacetophenones and hydroxybenzaldehydes in the presence of boric acid, in a mixed solvent system.

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