Benzene, (heptylthio)-

Base Information Edit

Chemical Name:Benzene, (heptylthio)-
CAS No.:13910-15-1
Molecular Formula:C13H20S
Molecular Weight:208.368
Hs Code.:
DSSTox Substance ID:DTXSID10483380
Nikkaji Number:J824.882F
Wikidata:Q82320662
Mol file:13910-15-1.mol

Synonyms:Benzene, (heptylthio)-;heptyl phenyl sulfide;13910-15-1;n-heptyl phenyl sulfide;SCHEMBL5694452;DTXSID10483380

Suppliers and Price of Benzene, (heptylthio)-

Supply Marketing:Edit

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

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Chemical Property of Benzene, (heptylthio)- Edit

Chemical Property:

Vapor Pressure:0.003mmHg at 25°C
XLogP3:5.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:7
Exact Mass:208.12857181
Heavy Atom Count:14
Complexity:116

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCSC1=CC=CC=C1

Technology Process of Benzene, (heptylthio)-

There total 13 articles about Benzene, (heptylthio)- 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: 92.0%

: 591-50-4
iodobenzene

: 1639-09-4
heptanethiol

: 13910-15-1
heptyl(phenyl)sulfane

Guidance literature:: With tetra(n-butyl)ammonium hydroxide; In water; at 50 ℃; for 24h; chemoselective reaction; Inert atmosphere; Sealed tube;
DOI:10.1039/c2ob06795a

Reference yield: 91.0%

: 1639-09-4
heptanethiol

: 108-90-7
chlorobenzene

: 13910-15-1
heptyl(phenyl)sulfane

Guidance literature:: With phenylzinc chloride lithium chloride; trans-[4,5-bis(diphenylphosphino)-9,9-dimethylxanthene](2-methylphenyl)nickel(II) chloride; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; at 0 - 20 ℃; for 0.25h; Reagent/catalyst; Temperature; Catalytic behavior; Schlenk technique; Inert atmosphere;
DOI:10.1021/acs.orglett.8b03476