4-Octylphenethyl methanesulfonate

Base Information

Chemical Name:4-Octylphenethyl methanesulfonate
CAS No.:162358-06-7
Molecular Formula:C17H28SO3
Molecular Weight:312.474
Hs Code.:
Mol file:162358-06-7.mol

Synonyms:Benzeneethanol,4-octyl-1-methanesulfonate;2-(4-Octylphenyl)ethyl 1-Methanesulfonate;4-OCTYLPHENETHYLMETHANESULFONATE;

Suppliers and Price of 4-Octylphenethyl methanesulfonate

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

TRC
2-(4-Octylphenyl)ethyl1-Methanesulfonate
100mg
$ 1320.00

Medical Isotopes, Inc.
2-(4-Octylphenyl)ethyl1-Methanesulfonate
10 mg
$ 650.00

Total 21 raw suppliers

Chemical Property of 4-Octylphenethyl methanesulfonate

Chemical Property:

Boiling Point:454.8±24.0 °C(Predicted)
PSA：51.75000
Density:1.048±0.06 g/cm3 (20 oC 760 Torr)
LogP:5.18910
Storage Temp.:Refrigerator
Solubility.:Chloroform, Ethyl Acetate

Purity/Quality:

98%,99%, ^*data from raw suppliers

2-(4-Octylphenyl)ethyl1-Methanesulfonate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses An intermediate in the preparation of FTY720-d4 (F805002), a labelled derivative of ISP-1 (myriocin), a fungal metabolite of the Chinese herb Iscaria sinclarii as well as a structural analogue of Sphi ngosine. An intermediate in the preparation of FTY720-d4 (F805002), a labelled derivative of ISP-1 (myriocin), a fungal metabolite of the Chinese herb Iscaria sinclarii as well as a structural analogue of Sphingosine.

Technology Process of 4-Octylphenethyl methanesulfonate

There total 13 articles about 4-Octylphenethyl methanesulfonate 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: 95.0%

: 124-63-0
methanesulfonyl chloride

: 162358-05-6
2-(4-Octylphenyl)ethyl alcohol

: 162358-06-7
4-octylphenethyl methanesulfonate

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 5h;
DOI:10.1039/c3cc00181d

Reference yield: 95.0%

: 162358-06-7
4-octylphenethyl methanesulfonate

Guidance literature:

Reference yield:

: 162358-04-5
acetic acid 2-(4-octylphenyl)ethyl ester

: 162358-06-7
4-octylphenethyl methanesulfonate

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / NaOMe / methanol / 8 h / 20 °C

2: Et₃N / CH₂Cl₂ / 1 h

With sodium methylate; triethylamine; In methanol; dichloromethane;
DOI:10.1021/jo049885d