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Bis(2,4,6-trimethylphenyl)mercury

Base Information Edit
  • Chemical Name:Bis(2,4,6-trimethylphenyl)mercury
  • CAS No.:26562-17-4
  • Molecular Formula:C18H22 Hg
  • Molecular Weight:438.963
  • Hs Code.:
  • European Community (EC) Number:664-425-9
  • DSSTox Substance ID:DTXSID30398806
  • Mol file:26562-17-4.mol
Bis(2,4,6-trimethylphenyl)mercury

Synonyms:DIMESITYLMERCURY;Bis(2,4,6-trimethylphenyl)mercury;26562-17-4;DTXSID30398806;AKOS024432901

Suppliers and Price of Bis(2,4,6-trimethylphenyl)mercury
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
  • Sigma-Aldrich
  • DIMESITYLMERCURY Aldrich
  • 1ea
  • $ 57.00
Total 0 raw suppliers
Chemical Property of Bis(2,4,6-trimethylphenyl)mercury Edit
Chemical Property:
  • Melting Point:235 °C 
  • PSA:0.00000 
  • LogP:4.82150 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:2
  • Exact Mass:440.142794
  • Heavy Atom Count:19
  • Complexity:235
Purity/Quality:

DIMESITYLMERCURY Aldrich *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC(=C(C(=C1)C)[Hg]C2=C(C=C(C=C2C)C)C)C
Technology Process of Bis(2,4,6-trimethylphenyl)mercury

There total 4 articles about Bis(2,4,6-trimethylphenyl)mercury 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 cesium carbonate; In isopropyl alcohol; under Ar; i-PrOH added to mixt. of Hg acetate, B compd. and Cs2CO3; sealed; heated at 50-55°C (oil bath) for 12-20 h; cooled; solvent removed by rotary evapn.; extd. with toluene or toluene-THF; filtered; filtrate reduced to dryness by rotary evapn.; triturated with pentane; dried; recrystd. from THF-pentane; elem. anal.;
DOI:10.1016/j.jorganchem.2008.10.024
Guidance literature:
In tetrahydrofuran; to suspn. of HgCl2 in THF added mesityllithium at room temp.; stirred for 10 h; volatiles removed in vacuo; residue extd. with benzene; extract filteredthrough frit; filtrate slowly concd.;
DOI:10.1002/zaac.201100049
Guidance literature:
With ethanol; sodium iodide;
DOI:10.1021/ja01330a044
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