Licoflavonol

Base Information

Chemical Name:Licoflavonol
CAS No.:60197-60-6
Molecular Formula:C20H18O6
Molecular Weight:354.359
Hs Code.:2914501900
UNII:9E3F3Z8Y1E
DSSTox Substance ID:DTXSID50208938
Nikkaji Number:J18.301F
Wikidata:Q27272427
Metabolomics Workbench ID:25061
ChEMBL ID:CHEMBL600185
Mol file:60197-60-6.mol

Synonyms:Licoflavonol;60197-60-6;UNII-9E3F3Z8Y1E;3,5,7-Trihydroxy-2-(4-hydroxy-phenyl)-6-(3-methyl-but-2-enyl)-1-benzopyran-4-one;9E3F3Z8Y1E;3,5,7-trihydroxy-2-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)chromen-4-one;3,5,7-trihydroxy-2-(4-hydroxyphenyl)-6-(3-methylbut-2-en-1-yl)-4H-chromen-4-one;CHEMBL600185;SCHEMBL8050093;DTXSID50208938;CHEBI:175548;HY-N6583;LMPK12111978;4',5,7-Trihydroxy-6-prenylflavonol;AKOS040760516;MS-25514;CS-0034284;D84920;Q27272427;3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-6-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one;3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-6-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one, 9CI

Suppliers and Price of Licoflavonol

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

Crysdot
Licoflavonol 95+%
5mg
$ 860.00

ChemScene
Licoflavonol ≥99.0%
5mg
$ 780.00

ChemScene
Licoflavonol ≥99.0%
10mg
$ 1300.00

Arctom
Licoflavonol ≥98%
5mg
$ 339.00

AK Scientific
Licoflavonol
2mg
$ 725.00

Total 24 raw suppliers

Chemical Property of Licoflavonol

Chemical Property:

Vapor Pressure:2.16E-15mmHg at 25°C
Boiling Point:608.3°C at 760 mmHg
PKA:6.86±0.40(Predicted)
Flash Point:220.2°C
PSA：111.13000
Density:1.444g/cm³
LogP:3.79110
XLogP3:3.8
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:3
Exact Mass:354.11033829
Heavy Atom Count:26
Complexity:597

Purity/Quality:

≥98% ^*data from raw suppliers

Licoflavonol 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=CCC1=C(C2=C(C=C1O)OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)C

Technology Process of Licoflavonol

There total 5 articles about Licoflavonol 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: 32.0%

: 143724-72-5
5-Hydroxy-3,7-bis-methoxymethoxy-2-(4-methoxymethoxy-phenyl)-6-(3-methyl-but-2-enyl)-chromen-4-one

: 60197-60-6
Licoflavonol

Guidance literature:: With Dowex 50; In methanol; at 40 ℃; for 24h;

Reference yield:

: 520-18-3
kaempferol

: 60197-60-6
Licoflavonol

Guidance literature:: Multi-step reaction with 3 steps

1: 24 percent / K₂CO₃ / acetone / 8 h / Ambient temperature

2: 11 percent / K₂CO₃ / methanol / 10 h / Ambient temperature

3: 32 percent / Dowex 50 / methanol / 24 h / 40 °C

With Dowex 50; potassium carbonate; In methanol; acetone;

Reference yield:

: 143724-66-7
3,4',7-tris-O-methoxymethylkaempferol

: 60197-60-6
Licoflavonol

Guidance literature:: Multi-step reaction with 2 steps

1: 11 percent / K₂CO₃ / methanol / 10 h / Ambient temperature

2: 32 percent / Dowex 50 / methanol / 24 h / 40 °C

With Dowex 50; potassium carbonate; In methanol;