4-(Butylsulfanyl)but-1-ene

Base Information

Chemical Name:4-(Butylsulfanyl)but-1-ene
CAS No.:20218-02-4
Molecular Formula:C8H16S
Molecular Weight:144.281
Hs Code.:
DSSTox Substance ID:DTXSID10556008
Wikidata:Q82437472

Synonyms:4-(BUTYLSULFANYL)BUT-1-ENE;20218-02-4;but-3-enylbutylsulphide;DTXSID10556008

Suppliers and Price of 4-(Butylsulfanyl)but-1-ene

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
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price

Total 0 raw suppliers

Chemical Property of 4-(Butylsulfanyl)but-1-ene

Chemical Property:

PSA：25.30000
LogP:3.09580
XLogP3:3.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:6
Exact Mass:144.09727168
Heavy Atom Count:9
Complexity:59.6

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCSCCC=C

Technology Process of 4-(Butylsulfanyl)but-1-ene

There total 1 articles about 4-(Butylsulfanyl)but-1-ene 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:

: 106-97-8,9003-29-6,9021-92-5
n-butane

: 629-45-8
dibutyl disulfide

: 5943-31-7
di-n-butyl trisulfide

: 20218-02-4
but-3-enyl n-butyl sulphide

Guidance literature:: With S₈(AsF₆)2; In liquid sulphur dioxide; Yield given. Yields of byproduct given;
DOI:10.1039/c39850000377

Reference yield: 85.0%

: 125475-73-2
bis(acetonitrile)bromo(pentafluorophenyl)palladium(II)

: 20218-02-4
but-3-enyl n-butyl sulphide

: 182140-18-7
[Pd(Br)(C₄H₉SC₂H₄CHCH₂C₆F₅)]2

Guidance literature:: In dichloromethane; stirring (room temp., 2 h); evapn., pptn. on Et2O and n-hexane addn., filtering, washing (ether / n-hexane = 2 : 3), drying; elem. anal.;
DOI:10.1021/om9604076