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trans-(C6F5)(Ph2P(CH2)2C(CH3)2(CH2)3CH=CH2)2Pt(CC)2H

Base Information Edit
  • Chemical Name:trans-(C6F5)(Ph2P(CH2)2C(CH3)2(CH2)3CH=CH2)2Pt(CC)2H
  • CAS No.:952610-21-8
  • Molecular Formula:C54H59F5P2Pt
  • Molecular Weight:1060.08
  • Hs Code.:
  • Mol file:952610-21-8.mol
trans-(C<sub>6</sub>F<sub>5</sub>)(Ph<sub>2</sub>P(CH<sub>2</sub>)2C(CH<sub>3</sub>)2(CH<sub>2</sub>)3CH=CH<sub>2</sub>)2Pt(CC)2H

Synonyms:trans-(C6F5)(Ph2P(CH2)2C(CH3)2(CH2)3CH=CH2)2Pt(CC)2H

Suppliers and Price of trans-(C6F5)(Ph2P(CH2)2C(CH3)2(CH2)3CH=CH2)2Pt(CC)2H
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Chemical Property of trans-(C6F5)(Ph2P(CH2)2C(CH3)2(CH2)3CH=CH2)2Pt(CC)2H Edit
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Technology Process of trans-(C6F5)(Ph2P(CH2)2C(CH3)2(CH2)3CH=CH2)2Pt(CC)2H

There total 1 articles about trans-(C6F5)(Ph2P(CH2)2C(CH3)2(CH2)3CH=CH2)2Pt(CC)2H 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 HNEt2; copper(l) iodide; In tetrahydrofuran; dichloromethane; a Schlenk flask was charged with Pt-contg. compd. (0.323 mmol), CuI (0.065 mmol), CH2Cl2, and HNEt2, and cooled to -45°C; then H(CC)2H (5.17 mmol) in THF was added with stirring; cold bath was allowed to warm to 10°C for 3 h and removed; after an addnl. 2.5 h (orange supernatant/white ppt.), the solvent was removed by oil pump vac.; the residue was extd. with toluene; combined exts. were filtered through alumina column (toluene rinses); solvent was removed by oil pump vac.; elem. anal.;
Guidance literature:
With TMEDA; O2; copper(l) chloride; In acetone; a flask was charged with Pt-contg. compd. (0.264 mmol) and acetone; a Schlenk flask was charged with CuCl (0.51 mmol) and acetone, TMEDA was added with stirring during 0.5 h; O2 was bubbled through three-necked flask; heating to 65°C; after addn. of supernatant over 1.5 h and 0.5 h, the solvent was removedby rotary evapn. and oil pump vac.; toluene was added, and mixt. was tr ansferred to an alumina column; the column was eluted with toluene; the solvent was removed; elem. anal.;
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