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[5,15-bis(3,5-di-tert-butylphenyl)-10-phenyl-20-[p-(trimethylsilylethynyl)phenylethynyl]porphynato]nickel(II)

Base Information Edit
  • Chemical Name:[5,15-bis(3,5-di-tert-butylphenyl)-10-phenyl-20-[p-(trimethylsilylethynyl)phenylethynyl]porphynato]nickel(II)
  • CAS No.:1244778-22-0
  • Molecular Formula:C67H68N4NiSi
  • Molecular Weight:1016.08
  • Hs Code.:
  • Mol file:1244778-22-0.mol
[5,15-bis(3,5-di-tert-butylphenyl)-10-phenyl-20-[p-(trimethylsilylethynyl)phenylethynyl]porphynato]nickel(II)

Synonyms:[5,15-bis(3,5-di-tert-butylphenyl)-10-phenyl-20-[p-(trimethylsilylethynyl)phenylethynyl]porphynato]nickel(II)

Suppliers and Price of [5,15-bis(3,5-di-tert-butylphenyl)-10-phenyl-20-[p-(trimethylsilylethynyl)phenylethynyl]porphynato]nickel(II)
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Chemical Property of [5,15-bis(3,5-di-tert-butylphenyl)-10-phenyl-20-[p-(trimethylsilylethynyl)phenylethynyl]porphynato]nickel(II) Edit
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Technology Process of [5,15-bis(3,5-di-tert-butylphenyl)-10-phenyl-20-[p-(trimethylsilylethynyl)phenylethynyl]porphynato]nickel(II)

There total 1 articles about [5,15-bis(3,5-di-tert-butylphenyl)-10-phenyl-20-[p-(trimethylsilylethynyl)phenylethynyl]porphynato]nickel(II) 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 Pd2(C6H5CHCHCOCHCHC6H5)3; P(C6H5)3; CuI; In triethylamine; toluene; (inert atm.); stirring degassed soln. of porphyrin deriv., bromobenzene deriv., palladium compd., phosphine deriv. and CuI in dry toluene and triethylamine at 40°C for 2 h; filtration through silica, chromy. (silica gel, light petroleum ether/CH2Cl2 (5:1)), NMR and MS;
DOI:10.1039/c003715j
Guidance literature:
With tetrabutyl ammonium fluoride; In tetrahydrofuran; dichloromethane; at 20 ℃; for 0.25h; Inert atmosphere;
DOI:10.1039/c003715j
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