Octyl phenyl ether

Base Information

• Chemical Name: Octyl phenyl ether
• CAS No.: 1818-07-1
• Molecular Formula: C14H22 O
• Molecular Weight: 206.328
• Hs Code.: 2909309090
• DSSTox Substance ID: DTXSID1061994
• Nikkaji Number: J101.690C
• Wikidata: Q72497676
• Mol file: 1818-07-1.mol

Synonyms:n-Octyl Phenyl Ether;1818-07-1;(Octyloxy)benzene;Octyl phenyl ether;octoxybenzene;Benzene, (octyloxy)-;Ether, octyl phenyl;octyloxybenzene;octylphenyl ether;n-Octyloxybenzene;1-Phenoxyoctane;octyloxy-benzene;n-octylphenyl ether;(Octyloxy)benzene #;Octylphenylether;98%;SCHEMBL197384;(Octyloxy)benzene, AldrichCPR;DTXSID1061994;BAA81807;MFCD00191564;AKOS009159491;AS-57424;O0224;D91836

Chemical Property of Octyl phenyl ether

Chemical Property:

• Melting Point: 8°C
• Refractive Index: 1.4870 to 1.4910
• Boiling Point: 283.1°Cat760mmHg
• Flash Point: 109°C
• PSA: 9.23000
• Density: 0.901g/cm³
• LogP: 4.42590
• Storage Temp.: Inert atmosphere,Room Temperature
• XLogP3: 5.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 8
• Exact Mass: 206.167065321
• Heavy Atom Count: 15
• Complexity: 127

Purity/Quality:

98%,99%, ^*data from raw suppliers

n-Octyl Phenyl Ether min.98.0% ^*data from reagent suppliers

Safty Information:

• Statements: 36/37/38
• Safety Statements: 26-36/37/39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCOC1=CC=CC=C1

Technology Process of Octyl phenyl ether

There total 26 articles about Octyl 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: 100.0%

1-bromo-octane (111-83-1) + sodium phenoxide (139-02-6) → octyloxybenzene (1818-07-1)

Guidance literature:

poly<1-hydroxyethylene-co-1-(2-ethylsulf; In 1,4-dioxane; at 75 ℃; for 23h; Product distribution; Rate constant; other catalysts;

Reference yield: 98.0%

1-Iodooctane (629-27-6) + phenol (108-95-2,27073-41-2) → octyloxybenzene (1818-07-1)

Guidance literature:

With potassium carbonate; In butanone; for 12h; Heating;

Reference yield: 98.0%

4-(n-octyloxy)-iodobenzene (96693-06-0) → octyloxybenzene (1818-07-1)

Guidance literature:

With 2,2'-azobis(isobutyronitrile); hypophosphorous acid; sodium hydrogencarbonate; In ethanol; for 5h; Heating;

DOI:10.1246/bcsj.74.225

upstream raw materials:

1-bromo-octane

sodium phenoxide

n-octyl methanesulfonate

n-chlorooctane

Downstream raw materials:

4-octyloxy-benzenesulfonic acid amide

1,5-Diamino-4,8-dihydroxy-2-(4-octyloxy-phenyl)-anthraquinone

4,8-Diamino-1,5-dihydroxy-2-(4-octyloxy-phenyl)-anthraquinone

2-(trans-4-heptylcyclohexyl)-1-(4-octoxyphenyl)ethanone

Refernces

• 1、 Cesaretti, Alessio,Carlotti, Benedetta,Consiglio, Giuseppe,Del Giacco, Tiziana,Spalletti, Anna,Elisei, Fausto. "Inclusion of two push-pull N -methylpyridinium salts in anionic surfactant solutions: A comprehensive photophysical investigation". . p. 6658 - 6667. Retrieved 2015.
• 2、 Bouquillon, Sandrine,Courant, Thomas,Dean, Darrell,Gathergood, Nicholas,Morrissey, Saibh,Pegot, Bruce,Scammells, Peter J.,Singer, Robert D.. "Biodegradable ionic liquids: Selected synthetic applications". . p. 843 - 847. Retrieved 2007.
• 3、 Talanova, M. Yu.,Guojun,Karakhanov,Anisimov. "Mesoporous aromatic frameworks modified by metal chlorides in phenol alkylation with oct-1-ene". . p. 2083 - 2087. Retrieved 2020/01/21.