1,2-Diphenoxybenzene

Base Information

Chemical Name:1,2-Diphenoxybenzene
CAS No.:3379-37-1
Molecular Formula:C18H14O2
Molecular Weight:262.308
Hs Code.:2909309090
DSSTox Substance ID:DTXSID40955368
Nikkaji Number:J59.961A
Wikidata:Q27119801
Metabolomics Workbench ID:56216
Mol file:3379-37-1.mol

Synonyms:1,2-Diphenoxybenzene;Benzene, o-diphenoxy-;3379-37-1;o-Diphenoxybenzene;Benzene, 1,2-diphenoxy-;1,1'-[1,2-phenylenebis(oxy)]dibenzene;Benzene, diphenoxy-;diphenoxybenzene;1,2-Diphenoxybenzene #;SCHEMBL51822;CHEBI:39274;DTXSID40955368;Q27119801

Suppliers and Price of 1,2-Diphenoxybenzene

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 4 raw suppliers

Chemical Property of 1,2-Diphenoxybenzene

Chemical Property:

Boiling Point:203.3 °C (10 mmHg)
PSA：18.46000
LogP:5.27120
XLogP3:4.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:262.099379685
Heavy Atom Count:20
Complexity:239

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)OC2=CC=CC=C2OC3=CC=CC=C3

Technology Process of 1,2-Diphenoxybenzene

There total 8 articles about 1,2-Diphenoxybenzene 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: 95.0%

: 1,2-bis((η6-phenoxy-η5-cyclopentadienyl)iron)benzene hexafluorophosphate

: 102-54-5,55404-68-7
ferrocene

: 3379-37-1
1,2-diphenoxybenzene

Guidance literature:: In dichloromethane; acetonitrile; Irradiation (UV/VIS); addn. of diiron-complex dissolved in CH2Cl2/CH3CN to a photolysis tube, purging with N2 for 30 min, irradiation under intense visible light (Xenon lamp) for 4 h; concn. (vac.), column chromy., elution (hexane) gives yellow band of ferrocene, elution (hexane/CHCl3) gives benzene-compd., evapn. to dryness, elem. anal.;
DOI:10.1021/om00013a055

Reference yield: 89.0%

: 591-50-4
iodobenzene

: 120-80-9,19481-10-8,37349-32-9
benzene-1,2-diol

: 3379-37-1
1,2-diphenoxybenzene

Guidance literature:: With copper(l) iodide; iron(III)-acetylacetonate; potassium carbonate; In dimethyl sulfoxide; at 140 ℃; for 72h; Inert atmosphere;
DOI:10.1039/c1ob05155e

Reference yield: 85.0%

: 34883-46-0
1-(2-iodophenoxy)benzene

: 108-95-2,27073-41-2
phenol

: 3379-37-1
1,2-diphenoxybenzene

Guidance literature:: With 2-Picolinic acid; potassium phosphate; copper(l) iodide; In dimethyl sulfoxide; at 95 ℃; for 24h; Inert atmosphere;
DOI:10.1002/anie.201806405