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Diheptyl(diphenyl)stannane

Base Information Edit
  • Chemical Name:Diheptyl(diphenyl)stannane
  • CAS No.:103044-42-4
  • Molecular Formula:C26H40Sn
  • Molecular Weight:471.314
  • Hs Code.:
  • DSSTox Substance ID:DTXSID90547156
  • Wikidata:Q82425208
  • Mol file:103044-42-4.mol
Diheptyl(diphenyl)stannane

Synonyms:Diheptyl(diphenyl)stannane;103044-42-4;DTXSID90547156

Suppliers and Price of Diheptyl(diphenyl)stannane
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Diheptyl(diphenyl)stannane Edit
Chemical Property:
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:14
  • Exact Mass:472.215204
  • Heavy Atom Count:27
  • Complexity:304
Purity/Quality:
Safty Information:
  • Pictogram(s):  
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MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCC[Sn](CCCCCCC)(C1=CC=CC=C1)C2=CC=CC=C2
Technology Process of Diheptyl(diphenyl)stannane

There total 1 articles about Diheptyl(diphenyl)stannane 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:
Guidance literature:
With hydrogenchloride; In toluene; byproducts: BrMgCl; n-heptylmagnesium bromide added dropwise at 0°C over 30 min to stoich. amt. of organotin chloride suspended in toluene under inert atm.; mixt. refluxed for 6 h; cooled to room temp.; hydrolyzed with 7% HCl; org. layer sepd.; dried overnight (anhyd. Na2SO4); filtered; solvent evapd.; purified by vac. distn.; elem. anal.;
DOI:10.1081/SIM-120030432
Guidance literature:
In benzene; byproducts: C6H5Br; addn. of N,N-dibromoarenesulfonamide to a stirred soln. of dialkyldiphenylstannane under Ar with ice water cooling; stirring for 15 min at 20°C after end of exothermic react.; evapn. in vac.; crystn. of residue (toluene, petroleum ether); elem. anal.;
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