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Bromotris(2,4,6-trimethylphenyl)stannane

Base Information
  • Chemical Name:Bromotris(2,4,6-trimethylphenyl)stannane
  • CAS No.:6166-12-7
  • Molecular Formula:C27H33BrSn
  • Molecular Weight:556.173
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40521401
  • Wikidata:Q82385839
Bromotris(2,4,6-trimethylphenyl)stannane

Synonyms:Bromotris(2,4,6-trimethylphenyl)stannane;6166-12-7;DTXSID40521401

Suppliers and Price of Bromotris(2,4,6-trimethylphenyl)stannane
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Chemical Property of Bromotris(2,4,6-trimethylphenyl)stannane
Chemical Property:
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:3
  • Exact Mass:556.07877
  • Heavy Atom Count:29
  • Complexity:437
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC(=C(C(=C1)C)[Sn](C2=C(C=C(C=C2C)C)C)(C3=C(C=C(C=C3C)C)C)Br)C
Technology Process of Bromotris(2,4,6-trimethylphenyl)stannane

There total 3 articles about Bromotris(2,4,6-trimethylphenyl)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 water; hydrogen bromide; In diethyl ether; toluene; dropwise addn. of mesitylmagnesium bromide soln. (Et2O) to SnBr4 (toluene), refluxing (10 h), H2O and HBr (10 % aq.) addn., filtering; washing (H2O, NaHCO3 aq., H2O), drying (MgSO4), evapn., crystn. om MeOHaddn.;
DOI:10.1021/ja990389u
Guidance literature:
With Mg; In tetrahydrofuran; toluene; addn. of SnBr4 in toluene to a Grignard-soln. of Mg and of mesityl bromide in THF, refluxing for 3 h, hydrolysis with aq. soln. of HBr; extn. of aq. phase with diethyl ether, concn., crystn. from acetone;
DOI:10.1016/0022-328X(89)85162-9
Guidance literature:
With 1-iodoundecane; In dodecane; React. performed at 50°C in mixt. of dodecane and naphtalene under Ar.; Ratio of 1-hexene: methylcyclopentane >20:1; Kinetics;
DOI:10.1021/om00100a021
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