2-[4-(Phenylsulfanyl)phenoxy]ethan-1-ol

Base Information

Chemical Name:2-[4-(Phenylsulfanyl)phenoxy]ethan-1-ol
CAS No.:65962-17-6
Molecular Formula:C14H14O2S
Molecular Weight:246.33
Hs Code.:
DSSTox Substance ID:DTXSID50548447
Wikidata:Q82427157

Synonyms:65962-17-6;2-[4-(Phenylsulfanyl)phenoxy]ethan-1-ol;SCHEMBL10878453;DTXSID50548447

Suppliers and Price of 2-[4-(Phenylsulfanyl)phenoxy]ethan-1-ol

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of 2-[4-(Phenylsulfanyl)phenoxy]ethan-1-ol

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:246.07145086
Heavy Atom Count:17
Complexity:196

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)SC2=CC=C(C=C2)OCCO

Technology Process of 2-[4-(Phenylsulfanyl)phenoxy]ethan-1-ol

There total 4 articles about 2-[4-(Phenylsulfanyl)phenoxy]ethan-1-ol 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%

: 445283-57-8
4-phenylsulfanylphenoxyethyl tetrahydro-2H-pyran-2-yl ether

: 65962-17-6
4-(phenylthio)phenoxyethanol

Guidance literature:: With pyridinium p-toluenesulfonate; In methanol; at 20 ℃; for 16h;
DOI:10.1016/j.bmc.2017.10.016

Reference yield:

: 5633-55-6
4-phenylsulfanylphenol

: 65962-17-6
4-(phenylthio)phenoxyethanol

Guidance literature:: Multi-step reaction with 2 steps

1: anhydr. potassium carbonate / dimethylformamide / 8 h / 100 °C

2: lithium aluminum hydride / diethyl ether / Ambient temperature

With lithium aluminium tetrahydride; potassium carbonate; In diethyl ether; N,N-dimethyl-formamide;

Reference yield:

: 2-[2'-(4''-iodophenoxy)ethoxy]tetrahydro-2H-pyrane

: 65962-17-6
4-(phenylthio)phenoxyethanol

Guidance literature:: Multi-step reaction with 2 steps

1: ethylene glycol; copper(l) iodide / isopropyl alcohol / 80 °C / Inert atmosphere

2: pyridinium p-toluenesulfonate / methanol / 16 h / 20 °C

With copper(l) iodide; pyridinium p-toluenesulfonate; ethylene glycol; In methanol; isopropyl alcohol;
DOI:10.1016/j.bmc.2017.10.016