CAS 31721-94-5
:5,7-Dihydroxychromone
Description:
5,7-Dihydroxychromone, with the CAS number 31721-94-5, is a flavonoid compound characterized by its chromone backbone, which features two hydroxyl groups at the 5 and 7 positions. This structural arrangement contributes to its potential biological activities, including antioxidant, anti-inflammatory, and antimicrobial properties. The compound is typically found in various plant sources and is of interest in pharmacological research due to its ability to interact with biological systems. It exhibits solubility in organic solvents and may have limited solubility in water, which can influence its bioavailability and application in medicinal chemistry. Additionally, 5,7-dihydroxychromone can participate in various chemical reactions, making it a valuable intermediate in organic synthesis. Its derivatives are often explored for their therapeutic potential, particularly in the development of natural products and functional foods. Overall, 5,7-dihydroxychromone represents a significant compound in the study of flavonoids and their health benefits.
Formula:C9H6O4
InChI:InChI=1S/C9H6O4/c10-5-3-7(12)9-6(11)1-2-13-8(9)4-5/h1-4,10,12H
InChI key:InChIKey=NYCXYKOXLNBYID-UHFFFAOYSA-N
SMILES:OC1=C2C(=CC(O)=C1)OC=CC2=O
Synonyms:- 4H-1-benzopyran-4-one, 5,7-dihydroxy-
- 5,7-Dihydroxy-4-chromone
- 5,7-Dihydroxy-4H-1-benzopyran-4-one
- 5,7-Dihydroxychromone
- Chromone, 5,7-dihydroxy-
- 5,7-Dihydroxy-4H-chromen-4-one
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5,7-Dihydroxychromone
CAS:Formula:C9H6O4Purity:≥ 98.0%Color and Shape:Yellow powderMolecular weight:178.145,7-Dihydroxychromone (Standard)
CAS:5,7-Dihydroxychromone (Standard) is a reference standard for research and analysis in studies involving 5,7-Dihydroxychromone. 1. 5,7-Dihydroxychromone (5,7-Dihydroxy-4H-Chromen-4-One) isolated from DME is one of the active compounds that may contribute to regulate blood glucose levels. 2. 5,7-Dihydroxychromone exerts neuroprotective effect against 6-OHDA-induced oxidative stress and apoptosis by activating Nrf2/ARE signal . 3. 5,7-Dihydroxychromone induces the translocation of Nrf2 to the nucleus and increases Nrf2/ARE binding activity which results in the up-regulation of the expression of Nrf2-dependent antioxidant genes, including HO-1, NQO1, and GCLc.Formula:C9H6O4Molecular weight:178.14155,7-Dihydroxychromone
CAS:1.Formula:C9H6O4Purity:99.76% - ≥95%Color and Shape:Yellow SolidMolecular weight:178.14155,7-Dihydroxychromone
CAS:Oxygen-heterocyclic compoundFormula:C9H6O4Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:178.145,7-Dihydroxy-4H-chromen-4-one
CAS:5,7-Dihydroxy-4H-chromen-4-one is a natural flavonoid, which is a bioactive compound extracted from various plant sources. It acts as a potent antioxidant by scavenging free radicals and chelating metal ions, contributing to the reduction of oxidative stress in biological systems. This mode of action involves the donation of hydrogen atoms from its hydroxyl groups, which stabilizes reactive oxygen species and prevents cellular damage.Formula:C9H6O4Purity:Min. 95%Molecular weight:178.14 g/mol








