1-Ethyl-2-(ethylsulfanyl)benzene

Base Information

Chemical Name:1-Ethyl-2-(ethylsulfanyl)benzene
CAS No.:90927-72-3
Molecular Formula:C₁₀H₁₄S
Molecular Weight:166.287
Hs Code.:
DSSTox Substance ID:DTXSID10558906
Wikidata:Q82441382

Synonyms:1-Ethyl-2-(ethylthio)benzene;90927-72-3;1-Ethyl-2-(ethylsulfanyl)benzene;1-ethyl-2-ethylsulfanylbenzene;SCHEMBL14507031;DTXSID10558906;AKOS006272055

Suppliers and Price of 1-Ethyl-2-(ethylsulfanyl)benzene

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 3 raw suppliers

Chemical Property of 1-Ethyl-2-(ethylsulfanyl)benzene

Chemical Property:

XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:166.08162162
Heavy Atom Count:11
Complexity:101

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC1=CC=CC=C1SCC

Technology Process of 1-Ethyl-2-(ethylsulfanyl)benzene

There total 4 articles about 1-Ethyl-2-(ethylsulfanyl)benzene 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:

: 14092-00-3
methyl o-tolyl sulfide

: 74-88-4
methyl iodide

: 90927-72-3
1-Ethyl-2-(ethylthio)benzene

Guidance literature:: With n-butyllithium; potassium tert-butylate; Yield given. Multistep reaction; 1) hexane, -60 to -10 deg C, 2) hexane, RT, overnight;
DOI:10.1016/S0040-4020(01)90456-9

Reference yield:

: 100-68-5
methyl-phenyl-thioether

: 90927-72-3
1-Ethyl-2-(ethylthio)benzene

Guidance literature:: Multi-step reaction with 2 steps

1: 1) n-BuLi, anhydr. TMEDA, 2) MeOH / 1) r.t, 12h, 2) 0 deg C

2: n-butyllithium

With methanol; n-butyllithium; N,N,N,N,-tetramethylethylenediamine;
DOI:10.1016/S0040-4020(01)81368-5