41440-05-5 Usage
Description
5,7,8-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one, also known as tetrahydroxyflavone, is a flavonoid compound derived from apigenin with an additional hydroxy group at position 8. It possesses a unique chemical structure that contributes to its potential biological activities and applications.
Uses
Used in Pharmaceutical Industry:
5,7,8-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one is used as a pharmaceutical compound for its potential therapeutic effects. 5,7,8-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one's unique structure allows it to interact with various biological targets, making it a promising candidate for the development of new drugs.
Used in Antioxidant Applications:
In the field of nutrition and health, 5,7,8-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one is used as an antioxidant. Its ability to scavenge free radicals and protect cells from oxidative damage makes it a valuable ingredient in the development of health supplements and functional foods.
Used in Cosmetic Industry:
5,7,8-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one is used as an active ingredient in the cosmetic industry for its potential skin protective and anti-aging properties. Its antioxidant and anti-inflammatory activities contribute to its potential use in skincare products, promoting skin health and reducing the signs of aging.
Used in Agricultural Industry:
In agriculture, 5,7,8-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one can be used as a natural pesticide or fungicide due to its antimicrobial properties. Its ability to inhibit the growth of harmful microorganisms can help protect crops and improve their overall health and yield.
Used in Research and Development:
5,7,8-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one is also used as a research compound in various scientific studies. Its unique chemical structure and potential biological activities make it an interesting subject for further investigation, with the aim of discovering new applications and understanding its mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 41440-05-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,4 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 41440-05:
(7*4)+(6*1)+(5*4)+(4*4)+(3*0)+(2*0)+(1*5)=75
75 % 10 = 5
So 41440-05-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H10O6/c16-8-3-1-7(2-4-8)12-6-10(18)13-9(17)5-11(19)14(20)15(13)21-12/h1-6,16-17,19-20H
41440-05-5Relevant articles and documents
Flavone Glucosides from the Aerial Part of Scutellaria comosa
Karimov,Ostroushko, Yu. V.,Botirov, E. Kh.
, p. 545 - 546 (2019/07/02)
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Preparation method of flavonoids
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Paragraph 0235-0237, (2017/11/16)
The invention discloses a preparation method of flavonoids. The method comprises the following step: in a solvent, in the presence of iodine and a silver salt or in the presence of iodine and a copper salt, performing an iodination reaction on a compound 1 to obtain a compound 2. Raw materials used in the method are easy to acquire, and the method has high yields and simple post processes, and does not need column chromatography.
Synthetic Studies of the Flavone Derivatives. VIII. Synthesis of Kanzakiflavones and Their Isomers
Iinuma, Munekazu,Tanaka, Toshiyuki,Matsuura, Shin
, p. 1006 - 1010 (2007/10/02)
Kanzakiflavone-1 and -2, isolates from Iris Unguicularis, and their position isomers were synthesized to confirm the structures of the isolates.The differences among these flavones are discussed on the basis of spectral data.Keywords: kanzakiflavone-1; kanzakiflavone-2; 4',5-dihydroxy-7,8-methylenedioxyflavone; 6,7-methylenedioxy-4',5,8-trimethoxyflavone; 7,8-methylenedioxy-4',5,6-trimethoxyflavone; 3'-acetyl-4',5-dihydroxy-6,7-methylenedioxyflavone
