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Trichloro(4-chlorophenyl)stannane

Base Information Edit
  • Chemical Name:Trichloro(4-chlorophenyl)stannane
  • CAS No.:87669-43-0
  • Molecular Formula:C6H4Cl4Sn
  • Molecular Weight:336.62
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40517940
  • Mol file:87669-43-0.mol
Trichloro(4-chlorophenyl)stannane

Synonyms:Trichloro(4-chlorophenyl)stannane;87669-43-0;SCHEMBL11316802;DTXSID40517940

Suppliers and Price of Trichloro(4-chlorophenyl)stannane
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Trichloro(4-chlorophenyl)stannane Edit
Chemical Property:
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:0
  • Exact Mass:337.805963
  • Heavy Atom Count:11
  • Complexity:125
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC(=CC=C1Cl)[Sn](Cl)(Cl)Cl
Technology Process of Trichloro(4-chlorophenyl)stannane

There total 1 articles about Trichloro(4-chlorophenyl)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 AlCl3; In neat (no solvent); byproducts: CH3SiCl3; heated for 1 h to 125°C; stirred for 2 h; heated to 135-140°C and then at 145-150°C for 2 h; AlCl3 sepd.; vacuum-distd.; elem. anal.;
Guidance literature:
With NH3; In methanol; byproducts: NH4Cl; N2-atmosphere; addn. of Sn-compd. to mixt. of 4 equiv. ligand with concd. NH3, refluxing for 3 h; collection (filtration), washing (MeOH), drying (vac., over P2O5); elem. anal.;
DOI:10.1016/S0022-328X(99)00103-5
Guidance literature:
In methanol; chloroform; according to F. Huber et al., Appl. Organometal. Chem. 11 (1997) 869; carboxylate in MeOH, Sn-compd. in CHCl3; elem. anal.;
DOI:10.1016/S0022-328X(99)00103-5
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