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Indium, tris(phenylmethyl)-

Base Information
  • Chemical Name:Indium, tris(phenylmethyl)-
  • CAS No.:125706-16-3
  • Molecular Formula:C21H21In
  • Molecular Weight:388.218
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30469202
  • Mol file:125706-16-3.mol
Indium, tris(phenylmethyl)-

Synonyms:Indium, tris(phenylmethyl)-;125706-16-3;DTXSID30469202

Suppliers and Price of Indium, tris(phenylmethyl)-
Supply Marketing:
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 1 raw suppliers
Chemical Property of Indium, tris(phenylmethyl)-
Chemical Property:
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:6
  • Exact Mass:388.0682044
  • Heavy Atom Count:22
  • Complexity:235
Purity/Quality:

85.0-99.8% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C[In](CC2=CC=CC=C2)CC3=CC=CC=C3
Technology Process of Indium, tris(phenylmethyl)-

There total 2 articles about Indium, tris(phenylmethyl)- 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 diethyl ether; byproducts: MgCl2; a mixt. of InCl3 and PhCH2MgCl in Et2O is stirred at room temp., heating for 2 h under reflux (under Ar); removing of solvent in vac., the residual is dissolved in toluene, filtn., removing of solvent in vac., crystn., elem. anal.;
Guidance literature:
In diethyl ether; N2 atmosphere, dry and degassed solvent, addn. of 3 equiv. of Grignard reagent in the dark at room temperature dropwise to soln. of SnCl3 in Et2O with stirring, refluxing (2 h); removing solvent in vac., washing (pentane), extn. with benzene, removing solvent in vac., recrystn. from (Et2O); elem. anal.;
DOI:10.1039/DT9890001625
Guidance literature:
In toluene; Ar atm.; stirring (48 h, 20°C); filtn., drying (vac.); elem. anal.;
upstream raw materials:

indium(III) chloride

benzylmagnesium chloride

Downstream raw materials:

(C6H5CH2)2InBr

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