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574-84-5

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574-84-5 Usage

Description

7,8-DIHYDROXY-6-METHOXYCOUMARIN, also known as Fraxetin, is a coumarin compound derived from various plant sources. It possesses antioxidant and anti-inflammatory properties, along with the ability to act as a protective agent against hyperuricemia and renal dysfunction. Its unique chemical structure and bioactive properties make it a promising candidate for various applications in different industries.

Uses

Used in Pharmaceutical Industry:
7,8-DIHYDROXY-6-METHOXYCOUMARIN is used as a therapeutic agent for its antioxidant and anti-inflammatory properties, which can help in the treatment of various diseases and conditions. Its protective effects against hyperuricemia and renal dysfunction also make it a potential candidate for the development of drugs targeting these specific health issues.
Used in Nutraceutical Industry:
7,8-DIHYDROXY-6-METHOXYCOUMARIN can be used as an additive in the nutraceutical industry, where its antioxidant properties can contribute to the development of dietary supplements and functional foods. These products can help consumers maintain a healthy lifestyle and prevent the onset of various diseases.
Used in Cosmetic Industry:
In the cosmetic industry, 7,8-DIHYDROXY-6-METHOXYCOUMARIN can be utilized for its anti-inflammatory and antioxidant properties. It can be incorporated into skincare products, such as creams, lotions, and serums, to help reduce inflammation, protect the skin from oxidative stress, and promote overall skin health.
Used in Agricultural Industry:
7,8-DIHYDROXY-6-METHOXYCOUMARIN can also be applied in the agricultural industry as a natural pesticide or growth promoter. Its antioxidant and anti-inflammatory properties can help protect crops from various diseases and pests, while also promoting healthy growth and development.

Check Digit Verification of cas no

The CAS Registry Mumber 574-84-5 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 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 574-84:
(5*5)+(4*7)+(3*4)+(2*8)+(1*4)=85
85 % 10 = 5
So 574-84-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H8O5/c1-14-6-4-5-2-3-7(11)15-10(5)9(13)8(6)12/h2-4,12-13H,1H3

574-84-5 Well-known Company Product Price

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  • Sigma-Aldrich

  • (18224)  Fraxetin  analytical standard

  • 574-84-5

  • 18224-50MG

  • 1,547.91CNY

  • Detail
  • Aldrich

  • (254916)  7,8-Dihydroxy-6-methoxycoumarin  98%

  • 574-84-5

  • 254916-250MG

  • 4,299.75CNY

  • Detail

574-84-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 7,8-dihydroxy-6-methoxychromen-2-one

1.2 Other means of identification

Product number -
Other names 6-methoxy-7,8-dihydroxycoumarin

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:574-84-5 SDS

574-84-5Relevant articles and documents

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Fischer

, p. 516,523 (1937)

-

Benzopyranones and Their Sulfate Esters from Pelargonium sidoides

Hauer, Hermann,Germer, Stefan,Elsaesser, Jens,Ritter, Thomas

, p. 350 - 352 (2010)

Investigation of the benzopyranones from the roots of Pelargonium sidoides led to the identification of 15 benzopyranones, among them the novel compounds 12 and 14. Furthermore, benzopyranones 4 and 15 were detected in Pelargonium sidoides for the first time. Structure determinations were performed by one- and two-dimensional NMR spectroscopy. An HPLC system for the discrimination of these benzopyranones has been developed. Georg Thieme Verlag KG Stuttgart New York.

Total syntheses of the coumarin-containing natural products pimpinellin and fraxetin using Au(I)-catalyzed intramolecular hydroarylation (IMHA) chemistry

Cervi, Aymeric,Aillard, Paul,Hazeri, Nourallah,Petit, Laurent,Chai, Christina L. L.,Willis, Anthony C.,Banwell, Martin G.

, p. 9876 - 9882 (2013/10/22)

The title natural products (1 and 2, respectively) have been synthesized by Au(I)-catalyzed intramolecular hydroarylation (IMHA) of the relevant aryl propiolate esters (e.g., 13), which were themselves formed by reaction of the corresponding phenols with either 3-(trimethylsilyl)propiolic acid or propiolic acid and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride or dicyclohexylcarbodiimide. (±)-Purpurasol (3) was readily derived from fraxetin (2) by established procedures.

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