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1H-inden-1-yl(triphenyl)stannane

Base Information
  • Chemical Name:1H-inden-1-yl(triphenyl)stannane
  • CAS No.:1249-25-8
  • Molecular Formula:C27H22Sn
  • Molecular Weight:465.182
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60513085
  • Mol file:1249-25-8.mol
1H-inden-1-yl(triphenyl)stannane

Synonyms:1H-inden-1-yl(triphenyl)stannane;1249-25-8;DTXSID60513085;(1H-Inden-1-yl)(triphenyl)stannane

Suppliers and Price of 1H-inden-1-yl(triphenyl)stannane
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
  • Packaging
  • price
Total 2 raw suppliers
Chemical Property of 1H-inden-1-yl(triphenyl)stannane
Chemical Property:
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:4
  • Exact Mass:466.074353
  • Heavy Atom Count:28
  • Complexity:473
Purity/Quality:

99.90% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC=C(C=C1)[Sn](C2C=CC3=CC=CC=C23)(C4=CC=CC=C4)C5=CC=CC=C5
Technology Process of 1H-inden-1-yl(triphenyl)stannane

There total 5 articles about 1H-inden-1-yl(triphenyl)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:
In tetrahydrofuran; Ar atmosphere; dropwise addn. of indene in THF to soln. of MeYbI (15°C), stirring (40 min, 20°C), addn. of Ph3SnCl in THF, warming to 28°C, stirring (1 h); addn. of water, extn. (ether), drying of extract (over MgSO4);
DOI:10.1007/BF00949006
Guidance literature:
In Petroleum ether; refluxing, 12 h;;
DOI:10.1016/S0022-328X(00)84649-5
Guidance literature:
In diethyl ether; refluxing, 48 h;;
DOI:10.1021/jo01354a006
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