1-phenyl-2-phenoxypropane

Base Information

Chemical Name:1-phenyl-2-phenoxypropane
CAS No.:55631-08-8
Molecular Formula:C₁₅H₁₆O
Molecular Weight:212.291
Hs Code.:

Synonyms:1-phenyl-2-phenoxypropane

Suppliers and Price of 1-phenyl-2-phenoxypropane

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 0 raw suppliers

Chemical Property of 1-phenyl-2-phenoxypropane

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-phenyl-2-phenoxypropane

There total 8 articles about 1-phenyl-2-phenoxypropane 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: 64.0%

: 930-68-7
cyclohexenone

: 698-87-3,14898-87-4
3-phenyl-2-propanol

: 55631-08-8
1-phenyl-2-phenoxypropane

Guidance literature:: With N-hydroxyphthalimide; oxygen; copper(II) bis(trifluoromethanesulfonate); potassium iodide; In water; toluene; at 120 ℃; for 24h; sealed tube;
DOI:10.1002/anie.201200698

Reference yield: 34.0%

: 591-50-4
iodobenzene

: 698-87-3,14898-87-4
3-phenyl-2-propanol

: 55631-08-8
1-phenyl-2-phenoxypropane

Guidance literature:: With copper(l) iodide; 1,10-Phenanthroline; caesium carbonate; In toluene; for 48h; Inert atmosphere; Reflux;
DOI:10.1021/jacs.0c00199

Reference yield:

: 117860-73-8
1-chloro-1-phenyl-2-phenoxypropane

: 637-50-3
1-phenylpropene

: 55631-08-8
1-phenyl-2-phenoxypropane

Guidance literature:: With 2,2'-azobis(isobutyronitrile); trimethylstannane; In benzene; at 80 ℃; for 0.25h; Kinetics; other remperature; relative rate of β-scission to reduction; Arrhenius parameters for trans scission and cis-scission also with Arrhenius expressions for abstraction of Hydrogen from n-Bu3SnH by phenylethyl radical;
DOI:10.1021/jo00006a043