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603-56-5

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603-56-5 Usage

Description

Chrysosplenetin B is a tetramethoxyflavone that is the 3,6,7,3'-tetramethyl ether derivative of quercetagetin. It is a naturally occurring compound with potential applications in various fields due to its unique chemical structure and properties.

Uses

Used in Pharmaceutical Industry:
Chrysosplenetin B is used as a pharmaceutical compound for its potential therapeutic effects. It has been studied for its antioxidant, anti-inflammatory, and anti-cancer properties, making it a promising candidate for the development of new drugs targeting various diseases.
Used in Cosmetic Industry:
In the cosmetic industry, chrysosplenetin B is used as an active ingredient for its antioxidant and anti-inflammatory properties. It can be incorporated into skincare products to help protect the skin from environmental stressors and promote a healthy, youthful appearance.
Used in Agricultural Industry:
Chrysosplenetin B can be used in the agricultural industry as a natural pesticide or fungicide due to its antimicrobial properties. It can help protect crops from diseases and pests, reducing the need for synthetic chemicals and promoting sustainable farming practices.
Used in Food Industry:
In the food industry, chrysosplenetin B can be utilized as a natural preservative and antioxidant. It can help extend the shelf life of perishable products and maintain their nutritional value by protecting them from oxidation.
Used in Research and Development:
Chrysosplenetin B is also used in research and development for its potential applications in various scientific fields. Researchers can study its chemical properties and interactions with other compounds to develop new materials, drugs, or technologies.

Occurance

Chrysosplenetin B is a tetramethoxyflavone that is the 3,6,7,3'-tetramethyl ether derivative of quercetagetin. It has a role as an antiviral agent and a plant metabolite. It is a tetramethoxyflavone and a dihydroxyflavone. It derives from a quercetagetin. Chrysosplenetin B is an O-methylated flavonol. It can be found in the root of Berneuxia thibetica and in Chamomilla recutita.

Check Digit Verification of cas no

The CAS Registry Mumber 603-56-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 603-56:
(5*6)+(4*0)+(3*3)+(2*5)+(1*6)=55
55 % 10 = 5
So 603-56-5 is a valid CAS Registry Number.
InChI:InChI=1/C19H18O8/c1-23-11-7-9(5-6-10(11)20)17-19(26-4)16(22)14-12(27-17)8-13(24-2)18(25-3)15(14)21/h5-8,20-21H,1-4H3

603-56-5SDS

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 chrysosplenetin

1.2 Other means of identification

Product number -
Other names chrysosplenol B

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:603-56-5 SDS

603-56-5Upstream product

603-56-5Relevant articles and documents

O-methylation of flavonoids by cell-free extracts of calamondin orange

Brunet, Gunter,Ibrahim, Ragai K.

, p. 741 - 746 (2007/10/02)

Cell-free extracts of calamondin orange (Citrus mitis) catalysed the O-methylation of almost all hydroxyls of a number of flavonoids, indicating the existence in citrus tissues of ortho, meta, para and 3-O-methyltransferases. The latter, hitherto unreported enzyme, catalysed the formation of 3-O-methyl ethers of galangin and quercetin. The stepwise O-methylation of a number of compounds, especially quercetin and quercetagetin, tends to suggest a coordinated sequence of O-methylations on the surface of a multienzyme complex. The methyl acceptor abilities of the flavonoid substrates used are discussed in relation to their hydroxyl substitution patterns and their negative electron density distribution.

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