Eupatolitin

Base Information

Chemical Name:Eupatolitin
CAS No.:29536-44-5
Molecular Formula:C17H14 O8
Molecular Weight:346.293
Hs Code.:2914509090
UNII:9KB4QHZ4YG
DSSTox Substance ID:DTXSID80183724
Nikkaji Number:J94.544G
Wikipedia:Eupatolitin
Wikidata:Q5409931
Metabolomics Workbench ID:26077
Mol file:29536-44-5.mol

Synonyms:Eupatolitin;Eupatoletin;29536-44-5;9KB4QHZ4YG;2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-6,7-dimethoxychromen-4-one;3,3',4',5-tetrahydroxy-6,7-dimethoxyflavone;2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-6,7-dimethoxy-4H-1-benzopyran-4-one;4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-6,7-dimethoxy-;UNII-9KB4QHZ4YG;6-Methoxy-7-methylquercetin;CHEBI:81340;DTXSID80183724;HY-N10886;LMPK12112994;AKOS040735123;CS-0637328;3,5,3',4'-tetrahydroxy-6,7-dimethoxyflavone;C17788;Q5409931;FLAVONE, 3,3',4',5-TETRAHYDROXY-6,7-DIMETHOXY-

Suppliers and Price of Eupatolitin

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

Arctom
Eupatoletin
5mg
$ 468.00

Total 6 raw suppliers

Chemical Property of Eupatolitin

Chemical Property:

Vapor Pressure:2.94E-17mmHg at 25°C
Boiling Point:640oC at 760 mmHg
PKA:6.13±0.40(Predicted)
Flash Point:238.7oC
PSA：129.59000
Density:1.591g/cm3
LogP:2.29960
XLogP3:2.5
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:3
Exact Mass:346.06886740
Heavy Atom Count:25
Complexity:547

Purity/Quality:

99% ^*data from raw suppliers

Eupatoletin ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O)OC

Technology Process of Eupatolitin

There total 10 articles about Eupatolitin 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: 94.0%

: 124910-06-1
2-(3,4-Bis-benzyloxy-phenyl)-3,5-dihydroxy-6,7-dimethoxy-chromen-4-one

: 29536-44-5
3′-dimethoxy-5,6,4′-trihydroxyflavon

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; ethyl acetate;

Reference yield:

: 1312097-82-7
sesuvioside C

: 29536-44-5
3′-dimethoxy-5,6,4′-trihydroxyflavon

: 3615-41-6,478518-52-4
L-Rhamnose

: 59-23-4
D-Galactose

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; water; at 80 ℃; for 4h;
DOI:10.1016/j.tet.2011.04.041

Reference yield:

: 1592-48-9
3,4-bis-benzyloxy-benzoic acid-anhydride

: 29536-44-5
3′-dimethoxy-5,6,4′-trihydroxyflavon

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) potassium benzoate, 2.) K₂CO₃ / 1.) 170/180 deg C, 8 h, 2.) acetone, reflux, 2.5-4 h

2: 90 percent / AlBr₃ / acetonitrile / 0.33 h / 0 - 5 °C

3: 99 percent / K₂CO₃ / acetone / Heating

4: 90 percent / AlBr₃ / acetonitrile / 1 h / Ambient temperature

5: 87 percent / K₂CO₃ / methanol / 2 h / Heating

6: 94 percent / H₂ / 10percent palladium on charcoal / ethyl acetate; methanol

With aluminum tri-bromide; hydrogen; Potassium benzoate; potassium carbonate; palladium on activated charcoal; In methanol; ethyl acetate; acetone; acetonitrile;