Bis[3-(4-ethoxyphenyl)furan-2-yl]methanone

Base Information

Chemical Name:Bis[3-(4-ethoxyphenyl)furan-2-yl]methanone
CAS No.:21493-98-1
Molecular Formula:C13H12O3
Molecular Weight:
Hs Code.:
DSSTox Substance ID:DTXSID20703425
Wikidata:Q82635585

Synonyms:bis[3-(4-ethoxyphenyl)furan-2-yl]methanone;DTXSID20703425;AKOS030240262

Suppliers and Price of Bis[3-(4-ethoxyphenyl)furan-2-yl]methanone

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 3 raw suppliers

Chemical Property of Bis[3-(4-ethoxyphenyl)furan-2-yl]methanone

Chemical Property:

Vapor Pressure:4.68E-05mmHg at 25°C
XLogP3:6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:8
Exact Mass:402.14672380
Heavy Atom Count:30
Complexity:490

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC1=CC=C(C=C1)C2=C(OC=C2)C(=O)C3=C(C=CO3)C4=CC=C(C=C4)OCC

Technology Process of Bis[3-(4-ethoxyphenyl)furan-2-yl]methanone

There total 6 articles about Bis[3-(4-ethoxyphenyl)furan-2-yl]methanone 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:

: 527-69-5
2-furancarbonyl chloride

: 103-73-1
Phenetole

: 21493-98-1
(4-ethoxy-phenyl)-[2]furyl ketone

Guidance literature:: With aluminium trichloride; benzene;

Reference yield:

: 527-69-5
2-furancarbonyl chloride

: 21493-98-1
(4-ethoxy-phenyl)-[2]furyl ketone

Guidance literature:: Multi-step reaction with 2 steps

1: aluminium chloride; carbon disulfide; nitrobenzene

2: aq. NaOH solution

With carbon disulfide; sodium hydroxide; aluminium trichloride; nitrobenzene;

Reference yield:

: 93-99-2
benzoic acid phenyl ester

: 21493-98-1
(4-ethoxy-phenyl)-[2]furyl ketone

Guidance literature:: Multi-step reaction with 2 steps

1: aluminium chloride; carbon disulfide; nitrobenzene

2: aq. NaOH solution

With carbon disulfide; sodium hydroxide; aluminium trichloride; nitrobenzene;