3,3',7-Trihydroxy-4'-methoxyflavone

Base Information

Chemical Name:3,3',7-Trihydroxy-4'-methoxyflavone
CAS No.:57396-72-2
Molecular Formula:C₁₆H₁₂O₆
Molecular Weight:300.268
Hs Code.:
UNII:G6GM3SVD7Y
DSSTox Substance ID:DTXSID001167746
Nikkaji Number:J94.524B
Wikidata:Q110180038
Metabolomics Workbench ID:24652
ChEMBL ID:CHEMBL2017117
Mol file:57396-72-2.mol

Synonyms:3,3',7-Trihydroxy-4'-methoxyflavone;Fisetin 4'-methyl ether;57396-72-2;3,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)chromen-4-one;CHEMBL2017117;3,7,3'-trihydroxy-4'-methoxyflavone;4H-1-Benzopyran-4-one, 3,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-;3,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one;G6GM3SVD7Y;SCHEMBL4101098;CHEBI:174848;QVYSSMFEUBQBEU-UHFFFAOYSA-N;DTXSID001167746;BDBM50381000;LMPK12111569;3,3/',7-Trihydroxy-4/'-methoxyflavone;Flavone, 3,3',7-trihydroxy-4'-methoxy-;2-(4-Methoxy-3-oxidanyl-phenyl)-3,7-bis(oxidanyl)chromen-4-one;3,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-chromen-4-one #

Suppliers and Price of 3,3',7-Trihydroxy-4'-methoxyflavone

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
4-O-Methylfisetin
50mg
$ 815.00

Total 1 raw suppliers

Chemical Property of 3,3',7-Trihydroxy-4'-methoxyflavone

Chemical Property:

PSA：100.13000
LogP:2.58540
XLogP3:2.3
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:2
Exact Mass:300.06338810
Heavy Atom Count:22
Complexity:473

Purity/Quality:: 4-O-Methylfisetin ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3)O)O)O
Uses 4-O-Methylfisetin is a flavonoid that shows inhibitory effects on cAMP phosphodiesterase.

Technology Process of 3,3',7-Trihydroxy-4'-methoxyflavone

There total 3 articles about 3,3',7-Trihydroxy-4'-methoxyflavone 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:

: 143091-87-6
2-benzoyloxy-1-(2,4-dihydroxy-phenyl)-ethanone

: 3-acetoxy-4-methoxy-benzoic acid-anhydride

: 57396-72-2
3,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one

Guidance literature:: With triethylamine; at 170 ℃; anschliessend Erwaermen mit wss.-aethanol. Kalilauge;

Reference yield:

: 60444-56-6
3-acetoxy-4-methoxybenzoic acid

: 57396-72-2
3,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one

Guidance literature:: Multi-step reaction with 3 steps

1: SOCl₂

2: pyridine; H₂O

3: triethylamine / 170 °C / anschliessend Erwaermen mit wss.-aethanol. Kalilauge

With pyridine; thionyl chloride; water; triethylamine;

Reference yield:

: 90798-12-2
3-acetoxy-4-methoxy-benzoyl chloride

: 57396-72-2
3,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine; H₂O

2: triethylamine / 170 °C / anschliessend Erwaermen mit wss.-aethanol. Kalilauge

With pyridine; water; triethylamine;