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3,5-dihydroxy-7,8-dimethoxy-2-(4-methoxyphenyl)-4H-chromen-4-one is a flavonoid, a type of polyphenolic compound found in various plants. It possesses antioxidant, anti-inflammatory, and potentially anti-cancer properties. 3,5-dihydroxy-7,8-dimethoxy-2-(4-methoxyphenyl)-4H-chromen-4-one is known for its ability to scavenge free radicals, reducing oxidative stress and inflammation in the body. Research suggests that it may have potential therapeutic applications in the treatment of various diseases, including cancer, cardiovascular disease, and neurodegenerative disorders. Additionally, it has been studied for its role in promoting skin health and wound healing.
Used in Pharmaceutical Industry:
3,5-dihydroxy-7,8-dimethoxy-2-(4-methoxyphenyl)-4H-chromen-4-one is used as a potential therapeutic agent for the treatment of various diseases such as cancer, cardiovascular disease, and neurodegenerative disorders. Its antioxidant, anti-inflammatory, and anti-cancer properties make it a promising candidate for pharmaceutical applications.
Used in Dietary Supplements:
3,5-dihydroxy-7,8-dimethoxy-2-(4-methoxyphenyl)-4H-chromen-4-one is used as a dietary supplement to support overall health and well-being. Its antioxidant and anti-inflammatory properties can help reduce oxidative stress and inflammation in the body, promoting a healthy immune system and overall health.
Used in Skincare Industry:
3,5-dihydroxy-7,8-dimethoxy-2-(4-methoxyphenyl)-4H-chromen-4-one is used as an ingredient in skincare products for its potential role in promoting skin health and wound healing. Its antioxidant properties can help protect the skin from environmental damage and support the skin's natural healing process.
Used in Cosmetic Industry:
3,5-dihydroxy-7,8-dimethoxy-2-(4-methoxyphenyl)-4H-chromen-4-one is used as an ingredient in cosmetics for its potential skin health benefits. Its antioxidant and anti-inflammatory properties can help improve skin appearance and reduce signs of aging, making it a valuable component in cosmetic formulations.

571-72-2

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571-72-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 571-72-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,7 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 571-72:
(5*5)+(4*7)+(3*1)+(2*7)+(1*2)=72
72 % 10 = 2
So 571-72-2 is a valid CAS Registry Number.

571-72-2SDS

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 tambulin

1.2 Other means of identification

Product number -
Other names Herbacetin 7,8,4'-trimethyl ether

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:571-72-2 SDS

571-72-2Relevant academic research and scientific papers

3,5-Dihydroxy-7,8-dimethoxyflavones and revised structures for some natural flavones

Horie, Tokunaru,Tsukayama, Masao,Kawamura, Yasuhiko,Yamamoto, Shigeo

, p. 1491 - 1495 (2007/10/02)

Seven 3,5-dihydroxy-7,8-dimethoxyflavones were synthesized from the corresponding 3,5,7,8-tetramethoxyflavones using selective demethylation and protection of 3- or 5- methoxy group, and their properties were clarified by the UV and 1H NMR spec

STUDIES OF THE SELECTIVE O-ALKYLATION AND DEALKYLATION OF FLAVONOIDS. IX. A NEW METHOD FOR SYNTHESIZING 3,5-DIHYDROXY-7,8-DIMETHOXYFLAVONES FROM 3-HYDROXY-5,7,8-TRIMETHOXYFLAVONES

Horie, Tokunaru,Tsukayama, Masao,Kawamura, Yasuhiko,Yamamoto, Shigeo

, p. 4465 - 4472 (2007/10/02)

2-Hydroxy-3,4,6-trimethoxy-ο-(p-methoxybenzoyloxy)acetophenone was prepared fom 2,3,4,6-tetramethoxyacetophenone via the corresponding ο-bromoacetophenone.Cyclization of the acetophenone with p-methoxybenzoic anhydride by application of the Allan-Robinson

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