6068-76-4

Basic information

• Product Name: 3,2'-DIHYDROXYFLAVONE
• Synonyms: 2'-HYDROXYFLAVONOL;3,2'-DIHYDROXYFLAVONE
• CAS NO: 6068-76-4
• Molecular Formula: C₁₅H₁₀O₄
• Molecular Weight: 254.24
• Product Categories: Di-substituted Flavones
• Mol File: 6068-76-4.mol
• Article Data: 4

Chemical Properties

• Melting Point: 200-202°C
• Boiling Point: 436.6±45.0 °C(Predicted)
• Appearance: /
• Density: 1.472±0.06 g/cm3(Predicted)
• Storage Temp.: 4°C
• Solubility: DMSO (Slightly), Methanol (Slightly, Heated)
• PKA: 6.67±0.20(Predicted)
• CAS DataBase Reference: 3,2'-DIHYDROXYFLAVONE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,2'-DIHYDROXYFLAVONE(6068-76-4)
• EPA Substance Registry System: 3,2'-DIHYDROXYFLAVONE(6068-76-4)

Safety Data

• Hazardous Substances Data: 6068-76-4(Hazardous Substances Data)

Usage

Description

3,2'-Dihydroxyflavone is a type of flavonoid, which are naturally occurring compounds found in plants. These compounds are known for their antioxidant, anti-inflammatory, and anti-cancer properties. 3,2'-Dihydroxyflavone, in particular, is characterized by its unique structure that includes two hydroxyl groups at the 3 and 2' positions of the flavone backbone.

Uses

Used in Biotechnology Industry:
3,2'-Dihydroxyflavone is used as a method for increasing the isolation efficiency and autologous proliferation of urine-derived stem cells. This application is particularly relevant in the field of regenerative medicine, where stem cells are used to repair or replace damaged tissues and organs. The use of 3,2'-dihydroxyflavone in this context can potentially improve the yield and quality of stem cells obtained from urine, making the process more efficient and cost-effective.

Upstream product

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• 42220-77-9 (2E)-1-(2-hydroxyphenyl)-3-(2-methoxyphenyl)prop-2-en-1-one 
• 29219-03-2 3-hydroxy-2-(2-methoxy-phenyl)-chromen-4-one 
• 15131-80-3 trans-2,2'-dihydroxychalcone 

Downstream Products

• 105827-34-7 2-(2-hydroxyphenyl)-3-methoxy-4H-chromen-4-one 

Relevant articles and documents

Phototransformations of some 3-cyclohexenyloxychromenones: Synthesis of Spirocyclic compounds

The phototransformation of the 3-cyclohexenyloxychromenones by irradiation with a pyrex-filtered light from a 125 W Hg vapor lamp under an inert atmosphere into the spirocyclic fused xanthenones was described. The efficacy of the protocol depended upon th

Synthesis, antimicrobial activity and molecular docking of novel tetracyclic scaffolds incorporating a flavonoid framework with medium sized oxygen heterocycles

A convenient approach for the synthesis of novel tetracyclic scaffolds incorporating a flavonoid framework with medium sized heterocyclic rings (eight-, nine-, ten- and eleven-membered rings) containing two oxygen atoms from flavonols through alkylation using different dibromoalkanes was described. The synthesized compounds were established based on the spectral data and X-ray crystal structure for 6c. The synthesized compounds were evaluated for their in vitro antimicrobial activity. Docking studies were carried out for most active two compounds 6f and 6i.