((p-Octylphenoxy)methyl)oxirane

Base Information

• Chemical Name: ((p-Octylphenoxy)methyl)oxirane
• CAS No.: 4223-17-0
• Molecular Formula: C17H26 O2
• Molecular Weight: 262.392
• European Community (EC) Number: 224-174-4
• DSSTox Substance ID: DTXSID10962387
• Nikkaji Number: J175.753I
• Mol file: 4223-17-0.mol

Synonyms:((p-Octylphenoxy)methyl)oxirane;[(p-Octylphenoxy)methyl]oxirane;4223-17-0;EINECS 224-174-4;2-(4-octylphenoxymethyl)oxirane;2-[(4-octylphenoxy)methyl]oxirane;4-Octylphenylglycidyl ether;SCHEMBL283616;DTXSID10962387;2-(4-octyl-phenoxymethyl)oxirane;Oxirane, ((4-octylphenoxy)methyl)-

Chemical Property of ((p-Octylphenoxy)methyl)oxirane

Chemical Property:

• Vapor Pressure: 2.76E-05mmHg at 25°C
• Boiling Point: 368.1°Cat760mmHg
• Flash Point: 133.1°C
• PSA: 21.76000
• Density: 0.987g/cm³
• LogP: 4.36720
• XLogP3: 5.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 10
• Exact Mass: 262.193280068
• Heavy Atom Count: 19
• Complexity: 221

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCC1=CC=C(C=C1)OCC2CO2

Technology Process of ((p-Octylphenoxy)methyl)oxirane

There total 2 articles about ((p-Octylphenoxy)methyl)oxirane 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%

p-Octylphenol (1806-26-4) + epichlorohydrin (106-89-8,24969-06-0,13403-37-7) → 2-[(4-octylphenoxy)methyl]oxirane (4223-17-0)

Guidance literature:

With potassium hydroxide; tetrabutylammomium bromide; at 20 ℃; for 5h;

DOI:10.1021/jm051243a

Reference yield:

→ 2-[(4-octylphenoxy)methyl]oxirane (4223-17-0)

Guidance literature:

Oxiran I, entspr. Phenol;

Reference yield: 99.0%

2-[(4-octylphenoxy)methyl]oxirane (4223-17-0) → 1-bromo-3-(4-octylphenoxy)propan-2-ol (741606-01-9)

Guidance literature:

With silica gel; lithium bromide; In dichloromethane; at 20 ℃; for 3h;

DOI:10.1021/jm051243a

upstream raw materials:

p-Octylphenol

epichlorohydrin

Downstream raw materials:

1-(indol-1-yl)-3-(4-octylphenoxy)propan-2-ol

1-(5-methoxyindol-1-yl)-3-(4-octylphenoxy)propan-2-ol

1-[2-hydroxy-3-(4-octylphenoxy)propyl]indole-5-carbonitrile

3-formyl-1-[2-hydroxy-3-(4-octylphenoxy)propyl]indole-5-carboxylic acid tert-butyl ester

Refernces