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Dracorhodin, a red-purple pigment extracted from the roots of the medicinal herb Dracaena cochinchinensis, is a natural chemical compound with a rich history in traditional Chinese medicine. Known for its antioxidant and anti-inflammatory properties, dracorhodin has been the subject of research for its potential therapeutic effects in cardiovascular disease and cancer treatment. Its diverse applications, from skincare to pharmaceuticals, are driven by its ability to combat oxidative stress and inflammation.

643-56-1

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643-56-1 Usage

Uses

Used in Traditional Chinese Medicine:
Dracorhodin is used as a therapeutic agent for its antioxidant and anti-inflammatory properties, traditionally employed to treat various ailments and promote overall health.
Used in Cardiovascular Disease Treatment:
Dracorhodin is used as a potential therapeutic agent for cardiovascular disease, leveraging its antioxidant properties to protect against oxidative stress and inflammation associated with heart conditions.
Used in Cancer Therapy:
Dracorhodin is used as a potential anti-cancer agent, with ongoing research exploring its ability to target and treat cancer cells while minimizing damage to healthy tissues.
Used in Skincare and Cosmetic Products:
Dracorhodin is used as an antioxidant ingredient in skincare and cosmetic products to protect the skin from environmental stressors and promote a youthful appearance.
Used in Pharmaceutical Research:
Dracorhodin is used as a subject of pharmaceutical research to further understand its health benefits and potential applications in the development of new treatments for various diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 643-56-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,4 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 643-56:
(5*6)+(4*4)+(3*3)+(2*5)+(1*6)=71
71 % 10 = 1
So 643-56-1 is a valid CAS Registry Number.
InChI:InChI=1/C17H14O3/c1-11-14(18)10-16-13(17(11)19-2)8-9-15(20-16)12-6-4-3-5-7-12/h3-10H,1-2H3

643-56-1SDS

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 5-methoxy-6-methyl-2-phenylchromen-7-one

1.2 Other means of identification

Product number -
Other names 5-Methoxy-6-methyl-2-phenyl-chromen-7-on

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:643-56-1 SDS

643-56-1Downstream Products

643-56-1Relevant academic research and scientific papers

Preparation methods of dracorhodin and salt and intermediates thereof and intermediate compounds

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Paragraph 0179; 0180; 0181; 0182, (2017/01/19)

The invention relates preparation methods of dracorhodin and salt and intermediates thereof and intermediate compounds. Synthesis of multifunctional group-substituted benzene ring core structures, that is, the intermediate compounds V, VI and VII is achieved by taking phloroglucinol trimethyl ether as a starting raw material, combining a formylation reaction, a Huang-Minlon reduction method, a methyl ether demethylation reaction, the reaction that benzyl is introduced onto phenolic hydroxyl through benzyl halogen, the reaction that methyl is introduced onto phenolic hydroxyl by taking dimethyl carbonate as a methylation reagent, a debenzylation reaction, a demethylation reaction and the like, utilizing the intramolecular hydrogen bond effect of formyl and phenolic hydroxyl on benzene rings and controlling the proper reaction conditions through proper combinations of the reactions and a protection-deprotection strategy. According to the method, dracorhodin and the salt thereof are synthesized by adopting the raw material which is low in cost, easy to obtain and low in toxicity, the process route is short, the cost is low, the chemical selectivity of all the steps is high, the total yield reaches up to about 10%, the process reproducibility is good, industrialization can be achieved, and the green and economical properties are achieved.

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