(Hexylselanyl)benzene

Base Information

Chemical Name:(Hexylselanyl)benzene
CAS No.:63866-88-6
Molecular Formula:C12H18Se
Molecular Weight:241.235
Hs Code.:
DSSTox Substance ID:DTXSID40503000
Nikkaji Number:J2.182.368F
Wikidata:Q82356474

Synonyms:(HEXYLSELANYL)BENZENE;phenylselenenylhexane;63866-88-6;DTXSID40503000

Suppliers and Price of (Hexylselanyl)benzene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of (Hexylselanyl)benzene

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:6
Exact Mass:242.05737
Heavy Atom Count:13
Complexity:106

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCC[Se]C1=CC=CC=C1

Technology Process of (Hexylselanyl)benzene

There total 17 articles about (Hexylselanyl)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: 97.0%

: 111-25-1
1-bromo-hexane

: 1666-13-3
diphenyl diselenide

: 63866-88-6
n-hexyl phenyl selenide

Guidance literature:: With sodium perchlorate; In methanol; electrolysis with (Mg)- ande and (Pt)-cathode;

Reference yield: 95.0%

: 1666-13-3
diphenyl diselenide

: Tetrahexylammonium borohydride

: 63866-88-6
n-hexyl phenyl selenide

Guidance literature:: In toluene; for 2h; Heating;
DOI:10.1055/s-1980-29126

Reference yield: 92.0%

: 17774-09-3
n-hexyl mercury chloride

: 63866-88-6
n-hexyl phenyl selenide

Guidance literature:: With diphenyl diselenide; In benzene; byproducts: Hg(SePh)2; Irradiation (UV/VIS); nitrogen atmosphere; mercurial and PhSeSePh (1.2 equiv) in deoxygenated solvent irradiated (275-W sunlamp, 35-40 °C, 2.5h);; filtration; solvent removed (vacuum); yield detd. by GLC after aq. Na2S2O3/CH2Cl2 extn.; n-BuSePh analysed by (1)H NMR, GLC and GCMS;;
DOI:10.1021/ja00219a030