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Tri-o-tolylbismuthine

Base Information Edit
  • Chemical Name:Tri-o-tolylbismuthine
  • CAS No.:10050-08-5
  • Molecular Formula:C21H21 Bi
  • Molecular Weight:482.378
  • Hs Code.:2931900090
  • DSSTox Substance ID:DTXSID70450290
  • Mol file:10050-08-5.mol
Tri-o-tolylbismuthine

Synonyms:Tri-o-tolylbismuthine;10050-08-5;Tris(2-methylphenyl)bismuthane;Tris(2-methylphenyl)bismuthine;tri-o-tolylbismuth;Bismuthine, tris(2-methylphenyl)-;trio-tolylbismuthine;DTXSID70450290;DWIMJCTYUMGECA-UHFFFAOYSA-N;MFCD00123270;AKOS015840503;AS-61346;FT-0757242;T1970;D92555

Suppliers and Price of Tri-o-tolylbismuthine
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
  • TCI Chemical
  • Tri-o-tolylbismuthine >98.0%(HPLC)(T)
  • 5g
  • $ 186.00
  • TCI Chemical
  • Tri-o-tolylbismuthine
  • 1G
  • $ 65.00
  • Chem-Impex
  • Tri-o-tolylbismuthine,98%(HPLC) 98%(HPLC)
  • 1G
  • $ 62.72
  • Chem-Impex
  • Tri-o-tolylbismuthine,98%(HPLC) 98%(HPLC)
  • 5G
  • $ 212.80
  • American Custom Chemicals Corporation
  • TRI-O-TOLYLBISMUTHINE 95.00%
  • 5G
  • $ 256.31
  • AK Scientific
  • Tri-o-tolylbismuthine
  • 5g
  • $ 311.00
Total 13 raw suppliers
Chemical Property of Tri-o-tolylbismuthine Edit
Chemical Property:
  • Melting Point:131.0 to 135.0 °C 
  • PSA:0.00000 
  • LogP:5.38560 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:3
  • Exact Mass:482.14472
  • Heavy Atom Count:22
  • Complexity:287
Purity/Quality:

98% *data from raw suppliers

Tri-o-tolylbismuthine >98.0%(HPLC)(T) *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC=CC=C1[Bi](C2=CC=CC=C2C)C3=CC=CC=C3C
Technology Process of Tri-o-tolylbismuthine

There total 34 articles about Tri-o-tolylbismuthine 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 C6H5SH; In benzene; byproducts: C6H5SSC6H5, H2NCOCF3; under Ar; a mixt. of the bismuthane, benzenethiol and benzene was stirred at 25°C for 3 h; the solvent was evapd. under vac., the oily residue was chromd. on silica gel (hexane/CH3CH2O2CCH3);
DOI:10.1021/ja003623l
Guidance literature:
With triphenylarsane; In benzene-d6; byproducts: (C6H5)3AsNCOCCl3; under Ar; a mixt. of the bismuthane, triphenylarsane and C6D6 was heatedat 60°C for 7 h;
DOI:10.1021/ja003623l
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