2-(Phenoxymethyl)-1,4,7,10,13-pentaoxacyclopentadecane

Base Information

Chemical Name:2-(Phenoxymethyl)-1,4,7,10,13-pentaoxacyclopentadecane
CAS No.:75507-16-3
Molecular Formula:C17H26O6
Molecular Weight:326.39
Hs Code.:
DSSTox Substance ID:DTXSID60504539

Synonyms:75507-16-3;2-(Phenoxymethyl)-1,4,7,10,13-pentaoxacyclopentadecane;SCHEMBL11049090;DTXSID60504539

Suppliers and Price of 2-(Phenoxymethyl)-1,4,7,10,13-pentaoxacyclopentadecane

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 2-(Phenoxymethyl)-1,4,7,10,13-pentaoxacyclopentadecane

Chemical Property:

XLogP3:1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:3
Exact Mass:326.17293854
Heavy Atom Count:23
Complexity:270

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1COCCOCC(OCCOCCO1)COC2=CC=CC=C2

Technology Process of 2-(Phenoxymethyl)-1,4,7,10,13-pentaoxacyclopentadecane

There total 5 articles about 2-(Phenoxymethyl)-1,4,7,10,13-pentaoxacyclopentadecane 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: 34.0%

: 37860-51-8
tetraethylene glycol di(p-toluenesulfonate)

: 538-43-2
3-phenoxy-1,2-propanediol

: 75507-16-3
<(Phenyloxy)methyl>-15-crown-5

Guidance literature:: With sodium hydride; In tetrahydrofuran; for 24h; Heating;
DOI:10.1021/ja00341a045

Reference yield:

: 122-60-1,71031-02-2
Phenyl glycidyl ether

: 75507-16-3
<(Phenyloxy)methyl>-15-crown-5

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / 72percent HClO₄ / H₂O / 80 °C

2: 34 percent / NaH / tetrahydrofuran / 24 h / Heating

With perchloric acid; sodium hydride; In tetrahydrofuran; water;
DOI:10.1021/ja00341a045

Reference yield:

: 108-95-2,27073-41-2
phenol

: 75507-16-3
<(Phenyloxy)methyl>-15-crown-5

Guidance literature:: Multi-step reaction with 3 steps

1: 2.) 50percent aq. NaOH / 1.) 80 deg C, 2.) 4 h

2: 78 percent / 72percent HClO₄ / H₂O / 80 °C

3: 34 percent / NaH / tetrahydrofuran / 24 h / Heating

With sodium hydroxide; perchloric acid; sodium hydride; In tetrahydrofuran; water;
DOI:10.1021/ja00341a045