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[[(CHC5H2N(C6H4(OC2H4)2OCH2))2]Cu(2,9-bis-(p-formylphenyl)-1,10-phenanthroline)](PF6)

Base Information Edit
  • Chemical Name:[[(CHC5H2N(C6H4(OC2H4)2OCH2))2]Cu(2,9-bis-(p-formylphenyl)-1,10-phenanthroline)](PF6)
  • CAS No.:165814-91-5
  • Molecular Formula:C60H50CuN4O8*F6P
  • Molecular Weight:1163.59
  • Hs Code.:
  • Mol file:165814-91-5.mol
[[(CHC<sub>5</sub>H<sub>2</sub>N(C<sub>6</sub>H<sub>4</sub>(OC<sub>2</sub>H<sub>4</sub>)2OCH<sub>2</sub>))2]Cu(2,9-bis-(p-formylphenyl)-1,10-phenanthroline)](PF<sub>6</sub>)

Synonyms:[[(CHC5H2N(C6H4(OC2H4)2OCH2))2]Cu(2,9-bis-(p-formylphenyl)-1,10-phenanthroline)](PF6)

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Chemical Property of [[(CHC5H2N(C6H4(OC2H4)2OCH2))2]Cu(2,9-bis-(p-formylphenyl)-1,10-phenanthroline)](PF6) Edit
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Technology Process of [[(CHC5H2N(C6H4(OC2H4)2OCH2))2]Cu(2,9-bis-(p-formylphenyl)-1,10-phenanthroline)](PF6)

There total 1 articles about [[(CHC5H2N(C6H4(OC2H4)2OCH2))2]Cu(2,9-bis-(p-formylphenyl)-1,10-phenanthroline)](PF6) 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 KPF6; In dichloromethane; under Ar; a soln. of Cu complex in CH3CN was added to a soln. of the macrocycle in CH2Cl2, after stirring for 20 min 2,9-bis(p-formylphenyl)-1,10-phenanthroline was added, the mixt. was stirred for 2 h; satd. soln. of KPF6 in H2O was added, the org. layer was extd. and evapd. to dryness;
DOI:10.1021/ja0119907
Guidance literature:
With trifluoroacetic acid; chloranil (tetrachloro-p-benzoquinone); KPF6; In dichloromethane; under Ar; to a soln. of the complex, the aldehyde and the (dipyrryl)methane in CH2Cl2 was added CF3CO2H, the mixt. was stirred for 16h at 25°C, the chloranil (tetrachloro-p-benzoquinone) was added, the mixt. was refluxed for 1.5 h; NaHCO3 was added, the org. layer was washed with H2O, a satd. soln. of KPF6 in H2O was added, the soln. was evapd., the residue was chromd. on SiO2 (CH2Cl2/MeOH) and then alumina (CH2Cl2);
DOI:10.1021/ja0119907
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