1-Phenyl-1-phenoxy-2-propene

Base Information

Chemical Name:1-Phenyl-1-phenoxy-2-propene
CAS No.:138621-80-4
Molecular Formula:C15H14O
Molecular Weight:210.276
Hs Code.:
DSSTox Substance ID:DTXSID90471341
Nikkaji Number:J2.001.908E
Mol file:138621-80-4.mol

Synonyms:1-phenyl-1-phenoxy-2-propene;138621-80-4;SCHEMBL3291158;DTXSID90471341;MNAOAMBRWJXLQM-UHFFFAOYSA-N;(+)-1-phenyl-1-phenoxy-2-propene

Suppliers and Price of 1-Phenyl-1-phenoxy-2-propene

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of 1-Phenyl-1-phenoxy-2-propene

Chemical Property:

XLogP3:4.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:210.104465066
Heavy Atom Count:16
Complexity:200

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CC(C1=CC=CC=C1)OC2=CC=CC=C2

Technology Process of 1-Phenyl-1-phenoxy-2-propene

There total 33 articles about 1-Phenyl-1-phenoxy-2-propene 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: 96.0%

: 21087-29-6
trans-3-phenylprop-2-enyl chloride

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

: 138621-80-4
1-phenyl-1-phenoxy-2-propene

Guidance literature:: trans-3-phenylprop-2-enyl chloride; With bis[dichloro(pentamethylcyclopentadienyl)ruthenium(III)]; potassium carbonate; In acetonitrile; at 20 ℃; for 0.333333h; Inert atmosphere; Schlenk technique;

phenol; In acetonitrile; at 20 ℃; for 16h; Solvent; regioselective reaction; Catalytic behavior; Inert atmosphere; Schlenk technique;
DOI:10.1016/j.tetlet.2013.12.074

Reference yield: 93.0%

: 21087-29-6
trans-3-phenylprop-2-enyl chloride

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

: 16519-25-8
(E)-cinnamyl phenyl ether

: 138621-80-4
1-phenyl-1-phenoxy-2-propene

Guidance literature:: trans-3-phenylprop-2-enyl chloride; With bis[dichloro(pentamethylcyclopentadienyl)ruthenium(III)]; potassium carbonate; In acetonitrile; at 20 ℃; for 0.333333h; Inert atmosphere; Schlenk technique;

phenol; In acetonitrile; at 20 ℃; for 16h; Solvent; regiospecific reaction; Catalytic behavior; Inert atmosphere; Schlenk technique;
DOI:10.1016/j.tetlet.2013.12.074