2-Naphthaleneethanol, 2-(4-methylbenzenesulfonate)

Base Information

Chemical Name:2-Naphthaleneethanol, 2-(4-methylbenzenesulfonate)
CAS No.:7175-35-1
Molecular Formula:C19H18O3S
Molecular Weight:326.416
Hs Code.:
DSSTox Substance ID:DTXSID501226767

Synonyms:7175-35-1;SCHEMBL5966607;XRFAOLIKBJIPII-UHFFFAOYSA-N;DTXSID501226767;EN300-37153453;2-Naphthaleneethanol, 2-(4-methylbenzenesulfonate);2-(naphthalen-2-yl)ethyl 4-methylbenzene-1-sulfonate;Toluene-4-sulfonic acid 2-naphthalen-2yl-ethyl ester

Suppliers and Price of 2-Naphthaleneethanol, 2-(4-methylbenzenesulfonate)

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-Naphthaleneethanol, 2-(4-methylbenzenesulfonate)

Chemical Property:

XLogP3:4.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:326.09766561
Heavy Atom Count:23
Complexity:460

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)OCCC2=CC3=CC=CC=C3C=C2

Technology Process of 2-Naphthaleneethanol, 2-(4-methylbenzenesulfonate)

There total 4 articles about 2-Naphthaleneethanol, 2-(4-methylbenzenesulfonate) 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: 91.0%

: 1485-07-0
naphthalen-2-ethanol

: 98-59-9
p-toluenesulfonyl chloride

: 7175-35-1
2-(naphthalen-2-yl)ethyl 4-methylbenzenesulfonate

Guidance literature:: With trimethylamine hydrochloride; triethylamine; at 0 ℃; for 1h; Inert atmosphere;
DOI:10.1016/j.bmc.2016.10.034

Reference yield:

: 1485-07-0
naphthalen-2-ethanol

: 4124-41-8
p-toluenesulfonylanhydride

: 7175-35-1
2-(naphthalen-2-yl)ethyl 4-methylbenzenesulfonate

Guidance literature:: With triethylamine; In tetrahydrofuran; at 20 ℃; for 1h;

Reference yield:

: 581-96-4
2-naphthylacetic acid

: 7175-35-1
2-(naphthalen-2-yl)ethyl 4-methylbenzenesulfonate

Guidance literature:: Multi-step reaction with 2 steps

1: LiAlH₄

2: (tosylation)

With lithium aluminium tetrahydride;
DOI:10.1021/ja00469a040