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6068-78-6

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6068-78-6 Usage

Description

2',3'-DIMETHOXY-3-HYDROXYFLAVONE is a synthetic flavonoid compound characterized by its unique chemical structure, which includes two methoxy groups at the 2' and 3' positions, and a hydroxyl group at the 3-position. 2',3'-DIMETHOXY-3-HYDROXYFLAVONE has been the subject of research due to its potential biological activities and applications in various fields.

Uses

Used in Pharmaceutical Industry:
2',3'-DIMETHOXY-3-HYDROXYFLAVONE is used as a therapeutic agent for its potential to improve endothelium-dependent relaxation in rats. This property makes it a promising candidate for the treatment of various cardiovascular diseases, as it may help to counteract the negative effects of oxygen radical generators on the endothelium.
Used in Research Applications:
In addition to its potential pharmaceutical applications, 2',3'-DIMETHOXY-3-HYDROXYFLAVONE is also used as a research tool to study the effects of flavonoids on endothelial function and to investigate the underlying mechanisms of their actions. This can contribute to a better understanding of the role of flavonoids in maintaining cardiovascular health and the development of new therapeutic strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 6068-78-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,6 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6068-78:
(6*6)+(5*0)+(4*6)+(3*8)+(2*7)+(1*8)=106
106 % 10 = 6
So 6068-78-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H10O5/c16-10-6-5-8(7-11(10)17)15-14(19)13(18)9-3-1-2-4-12(9)20-15/h1-7,16-17,19H

6068-78-6 Well-known Company Product Price

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  • Sigma

  • (SML0361)  3’,4’-Dihydroxyflavonol  ≥98% (HPLC)

  • 6068-78-6

  • SML0361-5MG

  • 666.90CNY

  • Detail
  • Sigma

  • (SML0361)  3’,4’-Dihydroxyflavonol  ≥98% (HPLC)

  • 6068-78-6

  • SML0361-25MG

  • 2,714.40CNY

  • Detail

6068-78-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,4-dihydroxyphenyl)-3-hydroxychromen-4-one

1.2 Other means of identification

Product number -
Other names 3',4'-dihydroxyflavonol

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:6068-78-6 SDS

6068-78-6Relevant articles and documents

2-substituted benzopyran-4-one compounds and application thereof

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Paragraph 0161; 0162; 0163; 0256; 0257; 0258, (2016/10/08)

The invention relates to the technical field of medicine and discloses 2-substituted benzopyran-4-one compounds with a structure shown in general formula I and an application of the compounds in preparation of antifungal drugs and synergistic antifungal drugs. The compounds can be jointly used with azole antifungal drugs, can improve sensibility of drug-resistance bacteria to the azole drugs, reverses drug resistance and produces a synergistic antifungal function.

NEUROPROTECTIVE POLYPHENOL ANALOGS

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Sheet 15/17, (2013/03/26)

The present invention provides neuroprotective polyphenol compounds, which can be synthetic analogs of fisetin, baicalein or chlorogenic acid, that maintain neuroprotective, anti-inflammatory, glutathione promoting, and/or antioxidant properties. The neur

Synthesis of novel 3,7-substituted-2-(3',4'-dihydroxyphenyl)flavones with improved antioxidant activity

Van Acker,Hageman,Haenen,Van der Vijgh,Bast,Menge

, p. 3752 - 3760 (2007/10/03)

A series of 3,7-disubstituted-2-(3',4'-dihydroxyphenyl)flavones was synthesized as potential cardioprotective agents in doxorubicin antitumor therapy. The influence of substituents on the 3 and 7 positions of the flavone nucleus on radical scavenging and

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