5-Hydroxy-7-methoxy-6-methylflavone

Base Information

Chemical Name:5-Hydroxy-7-methoxy-6-methylflavone
CAS No.:55969-57-8
Molecular Formula:C17H14 O4
Molecular Weight:282.296
Hs Code.:
NSC Number:641480
DSSTox Substance ID:DTXSID00327284
Nikkaji Number:J625.763A
Wikidata:Q82088907
Metabolomics Workbench ID:23256
ChEMBL ID:CHEMBL76553
Mol file:55969-57-8.mol

Synonyms:5-Hydroxy-7-methoxy-6-methylflavone;5-Hydroxy-7-methoxy-6-methylflavon;6-Methyltectochrysin;55969-57-8;NSC641480;5-Hydroxy-7-methoxy-6-methyl-2-phenyl-4H-chromen-4-one;CHEMBL76553;5-Hydroxy-7-methoxy-6-methyl-2-phenyl-chromen-4-one;5-hydroxy-7-methoxy-6-methyl-2-phenylchromen-4-one;SCHEMBL22068804;DTXSID00327284;CHEBI:174688;BDBM50338977;LMPK12110171;5-Hydroxy-6-methyl-7-methoxy-flavone;NSC-641480;NCI60_014034;5-Hydroxy-7-methoxy-6-methyl-2-phenyl-4H-1-benzopyran-4-one

Suppliers and Price of 5-Hydroxy-7-methoxy-6-methylflavone

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

Total 2 raw suppliers

Chemical Property of 5-Hydroxy-7-methoxy-6-methylflavone

Chemical Property:

Vapor Pressure:1.48E-10mmHg at 25°C
Boiling Point:498.3°Cat760mmHg
Flash Point:187.7°C
PSA：59.67000
Density:1.295g/cm³
LogP:3.48260
XLogP3:3.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:282.08920892
Heavy Atom Count:21
Complexity:425

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=CC=C3)OC

Technology Process of 5-Hydroxy-7-methoxy-6-methylflavone

There total 12 articles about 5-Hydroxy-7-methoxy-6-methylflavone 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:

Reference yield: 4.5%

: 480-40-0
5,7-dihydroxy-2-phenyl-chromen-4-one

: 74-88-4
methyl iodide

: 529-52-2
6-Methylchrysine

: 55969-57-8
5-hydroxy-7-methoxy-6-methyl-2-phenyl-chromen-4-one

Guidance literature:: With tetramethyl ammoniumhydroxide; tetraethylammonium iodide; In methanol; for 2h; Heating;
DOI:10.1021/jm991128y

Reference yield:

: 3-hydroxy-1-(2,6-dihydroxy-4-methoxy-3-methylphenyl)-3-phenylpropenone

: 14004-48-9
5-hydroxy-7-methoxy-8-methylflavone

: 55969-57-8
5-hydroxy-7-methoxy-6-methyl-2-phenyl-chromen-4-one

Guidance literature:: With Dichloromethyl methyl ether; tin(IV) chloride; In dichloromethane;
DOI:10.1016/j.tetlet.2006.09.110

Reference yield:

: 2657-28-5
2,4,6-trihydroxy-3-methyl-acetophenon

: 55969-57-8
5-hydroxy-7-methoxy-6-methyl-2-phenyl-chromen-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: sodium benzoate / anschliessendes Erwaermen mit wss.-aethanol. Kalilauge

2: potassium carbonate; acetone

With sodium benzoate; potassium carbonate; acetone;