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trans-[((2,6-bis[bis(trimethylsilyl)methyl]-4-[tris(trimethylsilyl)methyl]phenyl)dimethylphosphine)2dichloroplatinum]

Base Information Edit
  • Chemical Name:trans-[((2,6-bis[bis(trimethylsilyl)methyl]-4-[tris(trimethylsilyl)methyl]phenyl)dimethylphosphine)2dichloroplatinum]
  • CAS No.:404568-17-8
  • Molecular Formula:C64H146Cl2P2PtSi14
  • Molecular Weight:1636.99
  • Hs Code.:
  • Mol file:404568-17-8.mol
trans-[((2,6-bis[bis(trimethylsilyl)methyl]-4-[tris(trimethylsilyl)methyl]phenyl)dimethylphosphine)2dichloroplatinum]

Synonyms:trans-[((2,6-bis[bis(trimethylsilyl)methyl]-4-[tris(trimethylsilyl)methyl]phenyl)dimethylphosphine)2dichloroplatinum]

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Chemical Property of trans-[((2,6-bis[bis(trimethylsilyl)methyl]-4-[tris(trimethylsilyl)methyl]phenyl)dimethylphosphine)2dichloroplatinum] Edit
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Technology Process of trans-[((2,6-bis[bis(trimethylsilyl)methyl]-4-[tris(trimethylsilyl)methyl]phenyl)dimethylphosphine)2dichloroplatinum]

There total 1 articles about trans-[((2,6-bis[bis(trimethylsilyl)methyl]-4-[tris(trimethylsilyl)methyl]phenyl)dimethylphosphine)2dichloroplatinum] 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 benzene; under Ar atm. soln. BbtMe2P in benzene was added to aq. soln. K2PtCl4 atroom temp. and stirred for 7 days; ppt. was collected, washed with water, ethanol, and n-hexane; elem. anal.;
DOI:10.1246/bcsj.76.1577
Guidance literature:
With lithium naphthalenide; triphenylphosphane; In tetrahydrofuran; treated with 4 equiv. of Li compd. at -78°C, warmed to room temp.for 1 h with stirring, stirred 1 h at room temp., treated with sulfur a t -78°C, allowed to warm to room temp. for 4 h with stirring; solvent removed, CHCl3 added, filtered (Celite), evapd., ppt. dissolved (CHCl3), treated with triphenilphosphane at 50°C for 1 h, solventevapd., chromy. (gel permitation, CHCl3); elem. anal.;
DOI:10.1002/1521-3773(20020104)41:1<136::AID-ANIE136>3.0.CO;2-F
Guidance literature:
With lithium naphthalenide; triphenylphosphane; In tetrahydrofuran; byproducts: SeP(CH3)2(C6H2(CH(Si(CH3)3)2)2(C(Si(CH3)3)3)); treated with 4 equiv. of Li compd. at -78°C, warmed to room temp.for 1 h with stirring, stirred 1 h at room temp., treated with sulfur a t -78°C, allowed to warm to room temp. for 4 h with stirring; solvent removed, CHCl3 added, filtered (Celite), evapd., ppt. dissolved (CHCl3), treated with triphenilphosphane at 50°C for 1 h, solventevapd., chromy. (gel permitation, CHCl3); elem. anal.;
DOI:10.1002/1521-3773(20020104)41:1<136::AID-ANIE136>3.0.CO;2-F
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