Hibiscetin

Base Information

Chemical Name:Hibiscetin
CAS No.:577-24-2
Molecular Formula:C₁₅H₁₀O₉
Molecular Weight:334.239
Hs Code.:
DSSTox Substance ID:DTXSID101156102
Metabolomics Workbench ID:26355
Nikkaji Number:J94.462I
Wikidata:Q104253446
Mol file:577-24-2.mol

Synonyms:Hibiscetin;3,5,7,8-tetrahydroxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one;577-24-2;SCHEMBL12640014;DTXSID101156102;LMPK12113272;3,5,7,8,3',4',5'-heptahydroxyflavone;3,5,7,8-Tetrahydroxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one

Suppliers and Price of Hibiscetin

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 4 raw suppliers

Chemical Property of Hibiscetin

Chemical Property:

PSA：171.82000
LogP:1.39920
XLogP3:1.5
Hydrogen Bond Donor Count:7
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:1
Exact Mass:334.03248189
Heavy Atom Count:24
Complexity:535

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)O

Technology Process of Hibiscetin

There total 4 articles about Hibiscetin 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:

: 577-24-2
gossypetin

Guidance literature:: With sulfuric acid;

Reference yield:

: 110193-72-1
7-hydroxy-3,3',4',5,5',8-hexamethoxyflavone

: 577-24-2
gossypetin

Guidance literature:: With hydrogen iodide; acetic anhydride;

Reference yield:

: 42923-40-0
2,4-dihydroxy-3,6,ω-trimethoxyacetophenone

: 577-24-2
gossypetin

Guidance literature:: Multi-step reaction with 2 steps

1: sodium-<3,4,5-trimethoxy benzoate> / 180 °C / unter vermindertem Druck und Erwaermen des Reaktionsprodukts mit wss.-aethanol. Kalilauge

2: aqueous hydriodic acid; acetic acid anhydride

With hydrogen iodide; acetic anhydride; sodium 3,4,5-trimethoxybenzoate;