2,5-Diphenyl-3-[(propan-2-yl)oxy]furan

Base Information

Chemical Name:2,5-Diphenyl-3-[(propan-2-yl)oxy]furan
CAS No.:96324-33-3
Molecular Formula:C19H18O2
Molecular Weight:278.351
Hs Code.:
DSSTox Substance ID:DTXSID80539767
Nikkaji Number:J742.830H
Wikidata:Q82415569

Synonyms:96324-33-3;3-ISOPROPOXY-2,5-DIPHENYLFURAN;2,5-Diphenyl-3-[(propan-2-yl)oxy]furan;DTXSID80539767

Suppliers and Price of 2,5-Diphenyl-3-[(propan-2-yl)oxy]furan

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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Total 0 raw suppliers

Chemical Property of 2,5-Diphenyl-3-[(propan-2-yl)oxy]furan

Chemical Property:

XLogP3:5.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:278.130679813
Heavy Atom Count:21
Complexity:303

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)OC1=C(OC(=C1)C2=CC=CC=C2)C3=CC=CC=C3

Technology Process of 2,5-Diphenyl-3-[(propan-2-yl)oxy]furan

There total 1 articles about 2,5-Diphenyl-3-[(propan-2-yl)oxy]furan 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:

: 67-63-0,8013-70-5
isopropyl alcohol

: 96324-33-3
3-isopropoxy-2,5-diphenylfuran

Guidance literature:: With hydrogenchloride; triethylamine hydrochloride;
DOI:10.1021/ja01195a006

Reference yield: 95.0%

: 96324-33-3
3-isopropoxy-2,5-diphenylfuran

: cis-1,4-diphenyl-2-isopropoxy-2-butene-1,4-dione

Guidance literature:: With phenyltrimethylammonium tribromide; In tetrahydrofuran; dimethyl sulfoxide; at 20 ℃; for 22h;
DOI:10.3987/COM-05-10366