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3',4'-Dihydroxyflavone

Base Information
  • Chemical Name:3',4'-Dihydroxyflavone
  • CAS No.:4143-64-0
  • Molecular Formula:C15H10O4
  • Molecular Weight:254.242
  • Hs Code.:2914501900
  • UNII:KOH101S66V
  • DSSTox Substance ID:DTXSID70194349
  • Nikkaji Number:J354.017K
  • Wikidata:Q27282353
  • Pharos Ligand ID:R97KU3BT93N4
  • Metabolomics Workbench ID:74493
  • ChEMBL ID:CHEMBL222556
  • Mol file:4143-64-0.mol
3',4'-Dihydroxyflavone

Synonyms:3',4'-dihydroxy-flavone;3',4'-dihydroxyflavone

Suppliers and Price of 3',4'-Dihydroxyflavone
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 3'',4''-Dihydroxyflavone
  • 25mg
  • $ 45.00
  • TCI Chemical
  • 3',4'-Dihydroxyflavone >97.0%(T)
  • 1g
  • $ 400.00
  • TCI Chemical
  • 3',4'-Dihydroxyflavone >97.0%(T)
  • 200mg
  • $ 134.00
  • Biosynth Carbosynth
  • 3',4'-Dihydroxyflavone
  • 2 g
  • $ 500.00
  • Biosynth Carbosynth
  • 3',4'-Dihydroxyflavone
  • 100 mg
  • $ 60.00
  • Biosynth Carbosynth
  • 3',4'-Dihydroxyflavone
  • 250 mg
  • $ 100.00
  • Biosynth Carbosynth
  • 3',4'-Dihydroxyflavone
  • 1 g
  • $ 300.00
  • Biosynth Carbosynth
  • 3',4'-Dihydroxyflavone
  • 500 mg
  • $ 170.00
  • American Custom Chemicals Corporation
  • 3',4'-DIHYDROXY FLAVONE 95.00%
  • 100MG
  • $ 167.69
  • American Custom Chemicals Corporation
  • 3',4'-DIHYDROXY FLAVONE 95.00%
  • 500MG
  • $ 838.02
Total 23 raw suppliers
Chemical Property of 3',4'-Dihydroxyflavone
Chemical Property:
  • Melting Point:251-253 °C 
  • Boiling Point:482.3 °C at 760 mmHg 
  • PKA:8.29±0.18(Predicted) 
  • Flash Point:188.4 °C 
  • PSA:70.67000 
  • Density:1.443 g/cm3 
  • LogP:2.87120 
  • XLogP3:2.8
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:1
  • Exact Mass:254.05790880
  • Heavy Atom Count:19
  • Complexity:390
Purity/Quality:

97% *data from raw suppliers

3'',4''-Dihydroxyflavone *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O
Technology Process of 3',4'-Dihydroxyflavone

There total 17 articles about 3',4'-Dihydroxyflavone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sulfuric acid; In acetic acid; at 95 - 100 ℃; for 1h;
DOI:10.1021/jo00016a015
Guidance literature:
With pyridine hydrochloride; at 140 ℃; for 1h; Inert atmosphere;
DOI:10.1016/j.bmcl.2017.03.057
Guidance literature:
With 10% palladium hydroxide on charcoal; hydrogen; In ethanol; at 60 ℃; for 1h;
DOI:10.3987/COM-13-S(S)107
Refernces

Synthesis of new glycosylated flavonoids with inhibitory activity on cell growth

10.3390/molecules23051093

The research focuses on the synthesis and biological evaluation of new glycosylated flavonoids and xanthones with inhibitory activity on cell growth. The study involves the synthesis of four flavonoids (compounds 5, 6, 9, and 10) and one xanthone (compound 7) containing acetoglycoside moieties. Key chemicals used in the synthesis include rutin, diosmin, mangiferin, and 3,4-dihydroxyflavone as starting materials. Acetic anhydride and microwave irradiation were employed for acetylation, while 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide was used as the glucose donor for glycosylation. The synthesized compounds were evaluated for their in vitro cell growth inhibitory activity against six human tumor cell lines, including A375-C5, MCF-7, NCI-H460, U251, U373, and U87MG. The results showed that compound 10 exhibited the most potent inhibitory activity across all tested cell lines, with GI50 values < 8 μM and notable selectivity for cancer cells. The study highlights the importance of both acetylation and glycosylation in enhancing the biological activity of these compounds, providing insights for future development of more effective antitumor agents.

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