479-05-0

Basic information

• Product Name: flaviolin
• Synonyms: flaviolin;2,5,7-Trihydroxy-1,4-naphthalenedione;2,5,7-Trihydroxy-1,4-naphthoquinone
• CAS NO: 479-05-0
• Molecular Formula: C10H6O5
• Molecular Weight: 206.15
• Mol File: 479-05-0.mol
• Article Data: 6

Chemical Properties

• Melting Point: 250 °C (approx, decomp)(Solv: 1,4-dioxane (123-91-1))
• Boiling Point: 539.4°Cat760mmHg
• Flash Point: 294.1°C
• Appearance: /
• Density: 1.802g/cm³
• Vapor Pressure: 3.01E-12mmHg at 25°C
• Refractive Index: 1.785
• PKA: 4.50±1.00(Predicted)
• CAS DataBase Reference: flaviolin(CAS DataBase Reference)
• NIST Chemistry Reference: flaviolin(479-05-0)
• EPA Substance Registry System: flaviolin(479-05-0)

Safety Data

• Hazardous Substances Data: 479-05-0(Hazardous Substances Data)

Usage

Description

Flaviolin, also known as hydroxy-1,4-naphthoquinone, is a chemical compound with three hydroxy substituents placed at the 2-, 5-, and 7-positions on a 1,4-naphthoquinone structure. It is a naturally occurring compound found in various plants and has been studied for its potential applications in different industries.

Uses

Used in Pharmaceutical Industry:
Flaviolin is used as a pharmaceutical compound for its potential therapeutic properties. It has been studied for its antioxidant, anti-inflammatory, and antimicrobial activities, which could make it a valuable component in the development of new drugs for various health conditions.
Used in Cosmetic Industry:
In the cosmetic industry, flaviolin may be used as an active ingredient in skincare products due to its antioxidant properties. It could help protect the skin from environmental damage, promote skin health, and potentially slow down the aging process.
Used in Research and Development:
Flaviolin is also used in research and development for its unique chemical structure and properties. Scientists may study its interactions with other compounds and explore its potential applications in various fields, such as materials science or biotechnology.

InChI:InChI=1/C10H6O5/c11-4-1-5-9(6(12)2-4)7(13)3-8(14)10(5)15/h1-3,11-13H

Upstream product

• 18512-30-6 1,3,6,8-Tetrahydroxynaphthalene 
• 71741-18-9 6,8-Bis-benzyloxy-naphthalene-1,3-diol 
• 13586-04-4 3,6,8-trimethoxy-1-naphthol 
• 4724-10-1 methyl 2-(3,5-dihydroxyphenyl)acetate 
• 80457-61-0 methanesulfonyl 3,5-dibenzyloxybenzyl alcohol 
• 65857-78-5 methyl 2-acetyl-3,5-bis(benzyloxy)phenylacetate 
• 79762-35-9 methyl 2-(3,5-bis(benzyloxy)-2-formylphenyl)acetate 
• 58604-84-5 (3',5'-dibenzyloxy)phenylacetonitrile 
• 2732-96-9 3,5-dibenzyloxyphenylacetic acid 
• 24131-31-5 3,5-dibenzyloxybenzyl alcohol 
• 58605-10-0 methyl 3,5-bis(benzyloxy)benzoate 
• 126495-72-5 methyl 2-(2-acetyl-3,5-dihydroxyphenyl)acetate 
• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 49598-85-8 scytalone 

Downstream Products

• 5518-91-2 5-hydroxy-2,7-dimethoxy-1,4-naphthoquinone 

Relevant articles and documents

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Enantioselective total synthesis of (-)-napyradiomycin A1 via asymmetricchlorination of an isolated olefin

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Method for dyeing keratinous fibres using a monohydroxyindole or dihydroxyindole and a non-oxidizing aromatic carbonyl derivative and dyeing agent

The present invention relates to a method for dyeing keratinous fibers, characterized in that the following are applied to the fibers: a) a composition (A) containing, in a medium appropriate for dyeing, at least one monohydroxyindole or dihydroxyindole, this application being preceded or followed by the application of b) a composition (B) containing, in a medium appropriate for dyeing, at least one aromatic carbonyl derivative chosen from hydroxyacetophenones, hydroxybenzophenones, 2-hydroxy-1,4-benzoquinones, hydroxy-1,4-naphthoquinones,amino-1,4-naphthoquinones,hydroxy-9,10-anthraquinones and amino-9,10-anthraquinones. It also relates to the dyeing agents for carrying it out.