2-Phenylnaphtho[2,1-b]furan

Base Information

Chemical Name:2-Phenylnaphtho[2,1-b]furan
CAS No.:14385-54-7
Molecular Formula:C18H12O
Molecular Weight:244.293
Hs Code.:
DSSTox Substance ID:DTXSID80361186
Nikkaji Number:J865.840D
Wikidata:Q82143387
Mol file:14385-54-7.mol

Synonyms:2-phenylnaphtho[2,1-b]furan;2-phenylbenzo[e][1]benzofuran;14385-54-7;SCHEMBL11644851;DTXSID80361186;AN-660/12815005

Suppliers and Price of 2-Phenylnaphtho[2,1-b]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
Packaging
price

Total 2 raw suppliers

Chemical Property of 2-Phenylnaphtho[2,1-b]furan

Chemical Property:

PSA：13.14000
LogP:5.25300
XLogP3:5.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:244.088815002
Heavy Atom Count:19
Complexity:307

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=CC3=C(O2)C=CC4=CC=CC=C43

Technology Process of 2-Phenylnaphtho[2,1-b]furan

There total 28 articles about 2-Phenylnaphtho[2,1-b]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: 90.0%

: (E)-1-(2-styryl)-naphthalen-2-ol

: 14385-54-7
phenyl-2 naphto<2,1-b>furanne

Guidance literature:: With iodine; potassium carbonate; In tetrahydrofuran; at 20 ℃; for 2h;
DOI:10.1055/s-2006-944204

Reference yield: 90.0%

: 1-(2-phenylethenyl)-2-naphthalenol

: 14385-54-7
phenyl-2 naphto<2,1-b>furanne

Guidance literature:: With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; 5%-palladium/activated carbon; at 140 ℃; for 22h; under 760.051 Torr; Inert atmosphere;
DOI:10.1002/adsc.201600082

Reference yield: 85.0%

: (E)-1-(2-styryl)-naphthalen-2-ol

: 14385-54-7
phenyl-2 naphto<2,1-b>furanne

: 17,18-diphenyl-8,16-dihydro-8,16-ethanodinaphtho[2,1-b:2',1'-f][1,5]dioxocine

Guidance literature:: With Selectfluor; copper(l) chloride; In ethyl acetate; at 40 ℃; for 12h; Reagent/catalyst; Solvent; Temperature; diastereoselective reaction; Inert atmosphere;
DOI:10.1021/acs.orglett.9b03587