7-(Benzyloxy)-2-(3,4-dimethoxyphenyl)-5,6-dimethoxy-4H-chromen-4-one

Base Information

Chemical Name:7-(Benzyloxy)-2-(3,4-dimethoxyphenyl)-5,6-dimethoxy-4H-chromen-4-one
CAS No.:52378-71-9
Molecular Formula:C26H24O7
Molecular Weight:448.472
Hs Code.:
DSSTox Substance ID:DTXSID701140244
Mol file:52378-71-9.mol

Synonyms:52378-71-9;7-(Benzyloxy)-2-(3,4-dimethoxyphenyl)-5,6-dimethoxy-4H-chromen-4-one;4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-5,6-dimethoxy-7-(phenylmethoxy)-;SCHEMBL8068919;AELRYZAWWQQMCX-UHFFFAOYSA-N;DTXSID701140244;CS-0101738;7-benzyloxy-3',4',5,6-tetramethoxy flavone;2-(3,4-dimethoxyphenyl)-5,6-dimethoxy-7-phenylmethoxychromen-4-one;2-(3,4-Dimethoxyphenyl)-5,6-dimethoxy-7-(phenylmethoxy)-4H-1-benzopyran-4-one

Suppliers and Price of 7-(Benzyloxy)-2-(3,4-dimethoxyphenyl)-5,6-dimethoxy-4H-chromen-4-one

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
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price

Total 1 raw suppliers

Chemical Property of 7-(Benzyloxy)-2-(3,4-dimethoxyphenyl)-5,6-dimethoxy-4H-chromen-4-one

Chemical Property:

XLogP3:4.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:8
Exact Mass:448.15220310
Heavy Atom Count:33
Complexity:674

Purity/Quality:: NLT 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OCC4=CC=CC=C4)OC)OC)OC

Technology Process of 7-(Benzyloxy)-2-(3,4-dimethoxyphenyl)-5,6-dimethoxy-4H-chromen-4-one

There total 11 articles about 7-(Benzyloxy)-2-(3,4-dimethoxyphenyl)-5,6-dimethoxy-4H-chromen-4-one 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: 77.0%

: 4-benzyloxy-2-hydroxy-3',4',5,6-tetra methoxy chalcone

: 52378-71-9
7-(benzyloxy)-2-(3,4-dimethoxyphenyl)-6,7-dimethoxy-4H-chromen-4-one

Guidance literature:: With selenium(IV) oxide; In i-Amyl alcohol;

Reference yield: 76.0%

: (E)-1-(4-(benzyloxy)-6-hydroxy-2,3-dimethoxyphenyl)-3-(3,4-dimethoxyphenyl)prop-2-en-1-one

: 52378-71-9
7-(benzyloxy)-2-(3,4-dimethoxyphenyl)-6,7-dimethoxy-4H-chromen-4-one

Guidance literature:: With selenium(IV) oxide; In i-Amyl alcohol; at 140 ℃; for 7h;

Reference yield:

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

: 52378-71-9
7-(benzyloxy)-2-(3,4-dimethoxyphenyl)-6,7-dimethoxy-4H-chromen-4-one

Guidance literature:: Multi-step reaction with 7 steps

1: potassium carbonate / acetone / 60 °C

3: potassium hydroxide; pyridine / diethylene glycol; water / 100 °C

4: pyridine; dipotassium peroxodisulfate; tetraethylammonium hydroxide / water / 24 h / 20 °C

5: acetone / 5 h / Reflux

6: potassium hydroxide / ethanol / 20 °C

7: selenium(IV) oxide / i-Amyl alcohol / Reflux

With pyridine; selenium(IV) oxide; dipotassium peroxodisulfate; tetraethylammonium hydroxide; potassium carbonate; potassium hydroxide; In ethanol; i-Amyl alcohol; water; acetone; diethylene glycol;