2-[(4-Phenoxyphenoxy)methyl]oxirane

Base Information

• Chemical Name: 2-[(4-Phenoxyphenoxy)methyl]oxirane
• CAS No.: 84267-54-9
• Molecular Formula: C15H14O3
• Molecular Weight: 242.274
• DSSTox Substance ID: DTXSID90575232

Synonyms:2-[(4-phenoxyphenoxy)methyl]oxirane;84267-54-9;2-(4-phenoxyphenoxymethyl)oxirane;SCHEMBL6939833;DTXSID90575232;AKOS000200404;AKOS017282980;CS-0240075;EN300-22432;G40732;A1-30979;Z147642784

Chemical Property of 2-[(4-Phenoxyphenoxy)methyl]oxirane

Chemical Property:

• Boiling Point: 368.3±17.0 °C(Predicted)
• PSA: 30.99000
• Density: 1.185±0.06 g/cm3(Predicted)
• LogP: 3.25650
• XLogP3: 3.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 5
• Exact Mass: 242.094294304
• Heavy Atom Count: 18
• Complexity: 242

Purity/Quality:

2-[(4-Phenoxyphenoxy)methyl]oxirane ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1C(O1)COC2=CC=C(C=C2)OC3=CC=CC=C3

Technology Process of 2-[(4-Phenoxyphenoxy)methyl]oxirane

There total 2 articles about 2-[(4-Phenoxyphenoxy)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: 61.0%

1-phenoxy-4-allyloxybenzene (25345-76-0) → 2-[(4-phenoxyphenoxy)methyl]oxirane (84267-54-9)

Guidance literature:

With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; for 20h; Ambient temperature;

DOI:10.1002/hlca.19950780513

Reference yield: 23.0%

4-Phenoxyphenol (831-82-3) + epichlorohydrin (106-89-8,24969-06-0,13403-37-7) → 2-[(4-phenoxyphenoxy)methyl]oxirane (84267-54-9)

Guidance literature:

With caesium carbonate; In acetonitrile; at 85 ℃; for 16h;

DOI:10.1021/acsinfecdis.1c00175

Reference yield: 90.0%

2-[(4-phenoxyphenoxy)methyl]oxirane (84267-54-9) → 2RS-2,3-dihydroxy-1-(4-phenoxyphenoxy)propane (63837-30-9)

Guidance literature:

With perchloric acid; In tetrahydrofuran; for 48h; Ambient temperature;

DOI:10.1021/jm9607616

upstream raw materials:

1-phenoxy-4-allyloxybenzene

4-Phenoxyphenol

epichlorohydrin

Downstream raw materials:

4-phenoxyphenyl (R,S)-2-hydroxypropyl ether

2RS-2,3-dihydroxy-1-(4-phenoxyphenoxy)propane

(E)-2-[3-(4-phenoxyphenoxy)prop-1-en-1-yl]-2H-tetrazole

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