2-(2-Chlorophenoxy)oxane

Base Information

Chemical Name:2-(2-Chlorophenoxy)oxane
CAS No.:91427-36-0
Molecular Formula:C11H13ClO2
Molecular Weight:212.676
Hs Code.:
DSSTox Substance ID:DTXSID30571612
Nikkaji Number:J853.470E

Synonyms:2-(2-Chlorophenoxy)oxane;91427-36-0;SCHEMBL12429188;DTXSID30571612

Suppliers and Price of 2-(2-Chlorophenoxy)oxane

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 2-(2-Chlorophenoxy)oxane

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:212.0604073
Heavy Atom Count:14
Complexity:175

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCOC(C1)OC2=CC=CC=C2Cl

Technology Process of 2-(2-Chlorophenoxy)oxane

There total 1 articles about 2-(2-Chlorophenoxy)oxane 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%

: 110-87-2
3,4-dihydro-2H-pyran

: 95-57-8
2-monochlorophenol

: 91427-36-0
2-chlorophenyl tetrahydro-2H-2-pyranyl ether

Guidance literature:: With poly(4-vinylpyridine) supported copper(II) oxide nanoparticles; In dichloromethane; at 20 ℃; for 0.0166667h; chemoselective reaction;
DOI:10.1007/s13738-016-0887-x

Reference yield: 85.0%

: 1066-45-1
trimethyltin(IV)chloride

: 91427-36-0
2-chlorophenyl tetrahydro-2H-2-pyranyl ether

: 7440-23-5
sodium

: 866927-61-9
trimethyl(2-tetrahydro-2H-2-pyranyloxyphenyl)stannane

Guidance literature:: In ammonia; Irradiation (UV/VIS); under inert atm.; into flask cooled with acetone-liq. N2 was condensed NH3; Me3SnCl dissolved; Na added; 2-chlorophenyl tetrahydro-2H-2-pyranylether phosphate added; soln. irradiated with stirring for 4 h; quenched by adding NH4Cl in excess; NH3 allowed to evap.; residue treated (H2O); extd. (Et2O); extracts washed (brine); dried (MgSO4); solvent removed; as oil;
DOI:10.1016/j.jorganchem.2005.05.023