Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

Stannane, trichloro(2,4,6-trimethylphenyl)-

Base Information Edit
  • Chemical Name:Stannane, trichloro(2,4,6-trimethylphenyl)-
  • CAS No.:108343-64-2
  • Molecular Formula:C9H11Cl3Sn
  • Molecular Weight:344.255
  • Hs Code.:
  • Mol file:108343-64-2.mol
Stannane, trichloro(2,4,6-trimethylphenyl)-

Synonyms:

Suppliers and Price of Stannane, trichloro(2,4,6-trimethylphenyl)-
Supply Marketing:Edit
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 0 raw suppliers
Chemical Property of Stannane, trichloro(2,4,6-trimethylphenyl)- Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of Stannane, trichloro(2,4,6-trimethylphenyl)-

There total 4 articles about Stannane, trichloro(2,4,6-trimethylphenyl)- 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 toluene; N2-atmosphere; slow addn. of slight excess SnCl4 to Cu-compd. at -30°C, slow warming to room temp., stirring for 12 h, heating to 50°C for 1 h; filtration, removal of volatiles (vac.), recrystn. (hexanes, -55°C);
DOI:10.1021/om9901224
Guidance literature:
Multi-step reaction with 2 steps
1: acetonitrile
In acetonitrile;
Guidance literature:
In toluene; formation of suspension of mesityllithium from bromomesitylene and n-butyllithium in n-hexane and react. of suspension with tin tetrachloride in toluene at about 10°C; stirring of react. mixture 8h at room temp. and refluxing for 24h;; after sepn. of salts, fractionating distn. (113°C/0.03mbar);;
DOI:10.1016/0022-328X(91)80134-6
Post RFQ for Price