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20869-95-8

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20869-95-8 Usage

Description

5,7-Dihydroxy-3-methoxy-2-(4-methoxy-phenyl)-chromen-4-one, commonly known as cirsimaritin, is a naturally occurring flavonoid compound found in various plant sources, particularly Artemisia species. It is recognized for its diverse pharmacological activities, including antioxidant, anti-inflammatory, anti-cancer, and neuroprotective properties. Cirsimaritin's potential therapeutic applications have made it a significant subject of interest in medicinal chemistry and pharmacology.

Uses

Used in Pharmaceutical Industry:
Cirsimaritin is used as a therapeutic agent for its antioxidant properties, which can help combat oxidative stress and related conditions. Its anti-inflammatory effects make it a potential candidate for treating inflammatory diseases.
Used in Anticancer Applications:
In the field of oncology, cirsimaritin is utilized as an anti-cancer agent due to its ability to inhibit cancer cell growth and proliferation. It has been studied for its potential in treating various types of cancer, including those of the breast, lung, and pancreas, by modulating multiple signaling pathways involved in tumor progression.
Used in Neuroprotective Therapies:
Cirsimaritin is used as a neuroprotective agent, leveraging its potential to protect neurons from damage and degeneration. This makes it a candidate for the treatment of neurodegenerative diseases such as Alzheimer's and Parkinson's.
Used in Nutraceutical Industry:
Given its wide range of health benefits, cirsimaritin is also used in the development of nutraceutical products, which aim to improve overall health and well-being through natural compounds.
Used in Cosmetic Industry:
Due to its antioxidant and anti-inflammatory properties, cirsimaritin may also find application in the cosmetic industry for the development of skincare products designed to protect and rejuvenate the skin.

Check Digit Verification of cas no

The CAS Registry Mumber 20869-95-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,6 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 20869-95:
(7*2)+(6*0)+(5*8)+(4*6)+(3*9)+(2*9)+(1*5)=128
128 % 10 = 8
So 20869-95-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H14O6/c1-21-11-5-3-9(4-6-11)16-17(22-2)15(20)14-12(19)7-10(18)8-13(14)23-16/h3-8,18-19H,1-2H3

20869-95-8SDS

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 5,7-dihydroxy-3-methoxy-2-(4-methoxyphenyl)chromen-4-one

1.2 Other means of identification

Product number -
Other names 3',5,7-trihydroxy-3,4'-dimethoxyflavone

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:20869-95-8 SDS

20869-95-8Relevant articles and documents

Selective methylation of kaempferol via benzylation and deacetylation of kaempferol acetates

Mei, Qinggang,Wang, Chun,Yuan, Weicheng,Zhang, Guolin

, p. 288 - 293 (2015/03/31)

A strategy for selective mono-, di- and tri-O-methylation of kaempferol, predominantly on the basis of selective benzylation and controllable deacetylation of kaempferol acetates, was developed. From the selective deacetylation and benzylation of kaempferol tetraacetate (1), 3,4′,5,-tri-O-acetylkaempferol (2) and 7-O-benzyl-3,4′5,-tri-O-acetylkaempferol (8) were obtained, respectively. By controllable deacetylation and followed selective or direct methylation of these two intermediates, eight O-methylated kaempferols were prepared with 51-77% total yields from kaempferol.

3-Alkoxyflavone antiviral agents

-

, (2008/06/13)

Antiviral compositions containing 3-alkoxyflavone compounds as their active ingredients are disclosed.

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