Fe(C₂₀H₈N₄(C₆H₅)4)(CO)(C₅H₅N)

Base Information

Chemical Name:Fe(C₂₀H₈N₄(C₆H₅)4)(CO)(C₅H₅N)
CAS No.:53470-09-0
Molecular Formula:C₅₀H₃₃FeN₅O
Molecular Weight:775.692
Hs Code.:

Fe(C<sub>20</sub>H<sub>8</sub>N<sub>4</sub>(C<sub>6</sub>H<sub>5</sub>)4)(CO)(C<sub>5</sub>H<sub>5</sub>N)

Synonyms:Fe(C₂₀H₈N₄(C₆H₅)4)(CO)(C₅H₅N)

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Fe(C₂₀H₈N₄(C₆H₅)4)(CO)(C₅H₅N)

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Technology Process of Fe(C₂₀H₈N₄(C₆H₅)4)(CO)(C₅H₅N)

There total 4 articles about Fe(C₂₀H₈N₄(C₆H₅)4)(CO)(C₅H₅N) 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:

Reference yield:

: 67409-82-9
pyridine iron tetraphenylporphyrin

: 53470-09-0
Fe(C₂₀H₈N₄(C₆H₅)4)(CO)(C₅H₅N)

Guidance literature:: With carbon monoxide; In dichloromethane; under N2 at 21°C; Kinetics;
DOI:10.1021/ja00533a031

Reference yield:

: 17845-65-7
bis(piperidine)(5,10,15,20-tetraphenylporphyrinato)iron(II)

: 53470-09-0
Fe(C₂₀H₈N₄(C₆H₅)4)(CO)(C₅H₅N)

Guidance literature:: With pyridine; carbon monoxide; under N2 at room temp., deoxygenated pyridine or pyridine-soln. added to a soln. of Fe-compd. in deoxygenated toluene, CH2Cl2 or cyclohexane, CO bubbled through the soln. for 15 min;
DOI:10.1021/ja00533a031

Reference yield:

: 917-23-7,20998-75-8
5,10,15,20-tetraphenyl-21H,23H-porphine

: 1834-30-6,2140-52-5,3094-87-9
iron(II) acetate

: 53470-09-0
Fe(5,10,15,20-tetraphenylporphine)CO(pyridine)

Guidance literature:: With pyridine; carbon monoxide; In chloroform; acetic acid; a soln. of Fe(CH3COO)2 in CH3COOH was added dropwise to soln. of ligand and excess of pyridine in chloroform, the mixt. was heated at 57°C for 2.5 h, then the temp. was reduced to 0°C, CO slowly bubbled through the soln. for 1 h under N2; the soln. was sealed under CO and refrigerated overnight, ppt. was collected by filtration, washed with Et2O, dried under vac. at ambient temp.;