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(C6H5CH2C9H6)2ZrCl2

Base Information Edit
  • Chemical Name:(C6H5CH2C9H6)2ZrCl2
  • CAS No.:207924-79-6
  • Molecular Formula:C32H26Cl2Zr
  • Molecular Weight:572.688
  • Hs Code.:
  • Mol file:207924-79-6.mol
(C<sub>6</sub>H<sub>5</sub>CH<sub>2</sub>C<sub>9</sub>H<sub>6</sub>)2ZrCl<sub>2</sub>

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Chemical Property of (C6H5CH2C9H6)2ZrCl2 Edit
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Technology Process of (C6H5CH2C9H6)2ZrCl2

There total 3 articles about (C6H5CH2C9H6)2ZrCl2 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 n-BuLi; In tetrahydrofuran; toluene; (Ar); Standard Schlenk technique; n-BuLi added to soln. of ligand in THFat -78°C; warmed to room temp.; stirred for 4 h; solvent removed (vac.); toluene added; ZrCl4/toluene added dropwise at -78°C; wa rmed to room. temp.; stirred for 18 h; filtered through Celite pad; pad washed (toluene); filtrate concd.; crystd. at -18°C; elem. anal.;
DOI:10.1016/S0022-328X(00)00570-2
Guidance literature:
With n-butyllithium; In diethyl ether; hexane; toluene; N2-atmosphere; dropwise addn. of BuLi (in hexane) to indene derivative (in ether) at -78°C, warming to room temp., stirring for 30 min, dropwise addn. to 0.5 equiv. of Zr-complex (in PhMe), stirring overnight; filtration, solvent removal (reduced pressure), recrystn. (THF/hexane); elem. anal.;
DOI:10.1016/S0022-328X(98)00386-6
Guidance literature:
With n-butyllithium; In diethyl ether; hexane; byproducts: butane, LiCl; under inert atmosphere, standard Schlenk techniques; ligand dissolved inEt2O, cooled to -78°C; 1 equiv. of n-BuLi in n-hexane added slow ly; stirred at room temp. until gas evolution stopped; 0.5 equiv. of ZrCl4 added; stirred overnight; filtered over Na2SO4; solvent evapd.; washed with n-pentane;
DOI:10.1016/S0022-328X(00)00776-2
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