1-Ethynylsulfanylbutane

Base Information

Chemical Name:1-Ethynylsulfanylbutane
CAS No.:41863-13-2
Molecular Formula:C6H10S
Molecular Weight:114.211
Hs Code.:
DSSTox Substance ID:DTXSID50456038
Wikidata:Q82278237
Mol file:41863-13-2.mol

Synonyms:1-ethynylsulfanylbutane;41863-13-2;n-butylthioacetylene;SCHEMBL7062919;DTXSID50456038

Suppliers and Price of 1-Ethynylsulfanylbutane

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 1-Ethynylsulfanylbutane

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:114.05032149
Heavy Atom Count:7
Complexity:67.5

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCSC#C

Technology Process of 1-Ethynylsulfanylbutane

There total 1 articles about 1-Ethynylsulfanylbutane 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:

: 109-72-8,29786-93-4
n-butyllithium

: 60-29-7,927820-24-4
diethyl ether

: 108479-92-1
(Ξ)-1-butylsulfanyl-2-phenylsulfanyl-ethylene

: 41863-13-2
butyl ethynyl sulfide

: 6228-98-4
phenylthioacetylene

Guidance literature:: Product distribution;
DOI:10.1021/ja01522a059

Reference yield: 84.0%

: 41863-13-2
butyl ethynyl sulfide

: 100-52-7
benzaldehyde

: 106-47-8
4-chloro-aniline

: 4-Butylsulfanyl-6-chloro-2-phenyl-1,2-dihydro-quinoline

Guidance literature:: With (polyallyl)scanduium trifylamide ditriflate; In dichloromethane; acetonitrile; at 40 ℃; for 15h;
DOI:10.1021/ja961062l