7''-O-Methylsciadopitysin

Base Information

• Chemical Name: 7''-O-Methylsciadopitysin
• CAS No.: 22783-08-0
• Molecular Formula: C₃₄H₂₆O₁₀
• Molecular Weight: 594.574
• DSSTox Substance ID: DTXSID20945464
• Nikkaji Number: J356.062G,J92.490C
• Wikidata: Q82922819
• Metabolomics Workbench ID: 133197
• ChEMBL ID: CHEMBL378516
• Mol file: 22783-08-0.mol

Synonyms:7''-O-Methylsciadopitysin;3778-25-4;W 13;22783-08-0;4H-1-Benzopyran-4-one, 5-hydroxy-8-(5-(5-hydroxy-7-methoxy-4-oxo-4H-1-benzopyran-2-yl)-2-methoxyphenyl)-7-methoxy-2-(4-methoxyphenyl)-, (+)-;Amentoflavone 7,4',7'',4'''-tetramethyl ether;(+)-5-Hydroxy-8-(5-(5-hydroxy-7-methoxy-4-oxo-4H-1-benzopyran-2-yl)-2-methoxyphenyl)-7-methoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one;5-hydroxy-8-[5-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)-2-methoxyphenyl]-7-methoxy-2-(4-methoxyphenyl)chromen-4-one;SCHEMBL22459584;DTXSID20945464;VXQYICLHHMETFH-UHFFFAOYSA-N;7,4,7,4-O-methyl-amentoflavone;HY-N2756;C34H26O10;AKOS040754384;C34-H26-O10;MS-30570;XA161648;4',4''',7,7''-Tetramethoxyamentoflavone;CS-0023262;F82124;Amentoflavone-7,7",4?,4"'- tetramethyl ether;5-hydroxy-8-(5-(5-hydroxy-7-methoxy-4-oxo-4H-chromen-2-yl)-2-methoxyphenyl)-7-methoxy-2-(4-methoxyphenyl)-4H-chromen-4-one;5-Hydroxy-8-[5-(5-hydroxy-7-methoxy-4-oxo-4H-1-benzopyran-2-yl)-2-methoxyphenyl]-7-methoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one

Chemical Property of 7''-O-Methylsciadopitysin

Chemical Property:

• Vapor Pressure: 1.46E-27mmHg at 25°C
• Boiling Point: 813.5°Cat760mmHg
• Flash Point: 264.5°C
• Density: 1.391g/cm³
• XLogP3: 6.3
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 10
• Rotatable Bond Count: 7
• Exact Mass: 594.15259702
• Heavy Atom Count: 44
• Complexity: 1110

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)OC)O)OC

Technology Process of 7''-O-Methylsciadopitysin

There total 9 articles about 7''-O-Methylsciadopitysin 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:

isoginkgetin (548-19-6) + methyl iodide (74-88-4) → 7,4',7'',4'''-tetra-O-methylamentoflavone (3778-25-4,22783-08-0)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

amentoflavone (1617-53-4) + dimethyl sulfate (77-78-1) → 7,4',7'',4'''-tetra-O-methylamentoflavone (3778-25-4,22783-08-0)

Guidance literature:

With potassium carbonate; In acetone;

DOI:10.1016/S0031-9422(00)80326-X

Reference yield:

diazomethane (186581-53-3,908094-01-9,334-88-3) + podocarpusflavone A (22136-74-9) → 7,4',7'',4'''-tetra-O-methylamentoflavone (3778-25-4,22783-08-0)

Guidance literature:

In 1,4-dioxane;

DOI:10.1016/0031-9422(81)85236-3

upstream raw materials:

diazomethane

podocarpusflavone A

amentoflavone 4',7'',4'''-trimethyl ether

Amentoflavon

Downstream raw materials:

5,5'-diacetoxy-7,7'-dimethoxy-2'-(4-methoxy-phenyl)-2,8'-(4-methoxy-m-phenylene)-bis-chromen-4-one