Oxirane, [[4-[2-(2-methylpropoxy)ethoxy]phenoxy]methyl]-

Base Information

Chemical Name:Oxirane, [[4-[2-(2-methylpropoxy)ethoxy]phenoxy]methyl]-
CAS No.:88017-06-5
Molecular Formula:C₁₅H₂₂O₄
Molecular Weight:266.337
Hs Code.:
DSSTox Substance ID:DTXSID80442848

Synonyms:88017-06-5;Oxirane, [[4-[2-(2-methylpropoxy)ethoxy]phenoxy]methyl]-;SCHEMBL10754391;DTXSID80442848;AHRSYVWBGGNSDK-UHFFFAOYSA-N;3-(4-(2-(2-methylpropoxy)ethoxy)phenoxy)-1,2-epoxypropane

Suppliers and Price of Oxirane, [[4-[2-(2-methylpropoxy)ethoxy]phenoxy]methyl]-

Supply Marketing:

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

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Chemical Property of Oxirane, [[4-[2-(2-methylpropoxy)ethoxy]phenoxy]methyl]-

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:9
Exact Mass:266.15180918
Heavy Atom Count:19
Complexity:236

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)COCCOC1=CC=C(C=C1)OCC2CO2

Technology Process of Oxirane, [[4-[2-(2-methylpropoxy)ethoxy]phenoxy]methyl]-

There total 4 articles about Oxirane, [[4-[2-(2-methylpropoxy)ethoxy]phenoxy]methyl]- 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:

: 4963-16-0
2-(2-methylpropoxy)ethyl bromide

: 88017-06-5
3-(4-(2-(2-methylpropoxy)ethoxy)phenoxy)-1,2-epoxypropane

Guidance literature:: Multi-step reaction with 3 steps

1: 83.6 percent / K₂CO₃; NaI / acetone / 48 h / Heating

2: 86.5 percent / H₂ / 10 percent Pd/C / ethanol / 20 °C / 760 Torr

3: KOH / ethanol / 20 °C

With potassium hydroxide; hydrogen; potassium carbonate; sodium iodide; palladium on activated charcoal; In ethanol; acetone; 1: Etherification / 2: Hydrogenolysis / 3: Etherification;
DOI:10.1016/S0223-5234(99)00114-2

Reference yield:

: 103-16-2
4-Benzyloxyphenol

: 88017-06-5
3-(4-(2-(2-methylpropoxy)ethoxy)phenoxy)-1,2-epoxypropane

Guidance literature:: Multi-step reaction with 3 steps

1: 83.6 percent / K₂CO₃; NaI / acetone / 48 h / Heating

2: 86.5 percent / H₂ / 10 percent Pd/C / ethanol / 20 °C / 760 Torr

3: KOH / ethanol / 20 °C

With potassium hydroxide; hydrogen; potassium carbonate; sodium iodide; palladium on activated charcoal; In ethanol; acetone; 1: Etherification / 2: Hydrogenolysis / 3: Etherification;
DOI:10.1016/S0223-5234(99)00114-2

Reference yield:

: 258514-01-1
4-[2-(2-methylpropoxy)ethoxy]phenyl benzyl ether

: 88017-06-5
3-(4-(2-(2-methylpropoxy)ethoxy)phenoxy)-1,2-epoxypropane

Guidance literature:: Multi-step reaction with 2 steps

1: 86.5 percent / H₂ / 10 percent Pd/C / ethanol / 20 °C / 760 Torr

2: KOH / ethanol / 20 °C

With potassium hydroxide; hydrogen; palladium on activated charcoal; In ethanol; 1: Hydrogenolysis / 2: Etherification;
DOI:10.1016/S0223-5234(99)00114-2