Cinnamyl phenyl ether

Base Information

• Chemical Name: Cinnamyl phenyl ether
• CAS No.: 16519-25-8
• Molecular Formula: C15H14 O
• Molecular Weight: 210.276
• NSC Number: 86646
• Nikkaji Number: J1.083.142C,J883.918B
• Mol file: 16519-25-8.mol

Synonyms:(E)-cinnamyl phenyl ether;16519-25-8;cinnamyloxybenzene;Cinnamyl phenyl ether;NSC86646;(3-Phenylallyloxy)benzene;SCHEMBL1158152;BDBM86790;LLOUPYJHSJUFQI-JXMROGBWSA-N;NSC-86646;STK671370;[(E)-3-phenoxy-prop-1-enyl]-benzene;[(1E)-3-phenoxyprop-1-en-1-yl]benzene;SR-01000512178;SR-01000512178-1

Chemical Property of Cinnamyl phenyl ether

Chemical Property:

• Vapor Pressure: 6.8E-05mmHg at 25°C
• Boiling Point: 354.5°C at 760 mmHg
• Flash Point: 141.3°C
• Density: 1.057g/cm³
• XLogP3: 4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 210.104465066
• Heavy Atom Count: 16
• Complexity: 198

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)C=CCOC2=CC=CC=C2
• Isomeric SMILES: C1=CC=C(C=C1)/C=C/COC2=CC=CC=C2

Technology Process of Cinnamyl phenyl ether

There total 101 articles about Cinnamyl phenyl ether 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: 99.0%

ethyl (E)-3-phenyl-2-propenyl carbonate (106625-69-8) + phenol (108-95-2,27073-41-2) → (E)-cinnamyl phenyl ether (16519-25-8)

Guidance literature:

With carbon monoxide; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; triphenylphosphine; In tetrahydrofuran; at 50 ℃; for 6h; under 22800 Torr;

DOI:10.1016/0022-328X(95)05939-M

Reference yield: 99.0%

C16H14O3 (1200591-26-9) → phenyl 3-phenyl-allyl ether (37464-41-8,16519-25-8)

Guidance literature:

With triphenylphosphine; tetrabutylammonium tricarbonylnitrosylferrate; In tert-butyl methyl ether; at 80 ℃; regioselective reaction;

DOI:10.1021/ol902291z

Reference yield: 97.0%

Cinnamyl acetate (21040-45-9) + phenol (108-95-2,27073-41-2) → (E)-cinnamyl phenyl ether (16519-25-8)

Guidance literature:

With palladium 10% on activated carbon; cetyltrimethylammonim bromide; triphenylphosphine; In water; at 70 ℃; for 3h; Micellar solution; Green chemistry;

DOI:10.1021/jo401737t

upstream raw materials:

sodium phenoxide

Cinnamyl bromide

phenol

3-bromo-1-phenyl-1-propenyl bromide

Downstream raw materials:

3-phenoxypropylbenzene

2-(1-phenylallyl)phenol

5-Phenyl-hept-6-en-1-ol

styrylacetic acid