((CH₃OC₆H₄NCCH₃)2)((CH₃CH₂OCOCHCH)2)(CO)Fe

Base Information

Chemical Name:((CH₃OC₆H₄NCCH₃)2)((CH₃CH₂OCOCHCH)2)(CO)Fe
CAS No.:82134-11-0
Molecular Formula:C₂₉H₃₄FeN₂O₇
Molecular Weight:578.445
Hs Code.:

((CH<sub>3</sub>OC<sub>6</sub>H<sub>4</sub>NCCH<sub>3</sub>)2)((CH<sub>3</sub>CH<sub>2</sub>OCOCHCH)2)(CO)Fe

Synonyms:((CH₃OC₆H₄NCCH₃)2)((CH₃CH₂OCOCHCH)2)(CO)Fe

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Chemical Property of ((CH₃OC₆H₄NCCH₃)2)((CH₃CH₂OCOCHCH)2)(CO)Fe

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Technology Process of ((CH₃OC₆H₄NCCH₃)2)((CH₃CH₂OCOCHCH)2)(CO)Fe

There total 2 articles about ((CH₃OC₆H₄NCCH₃)2)((CH₃CH₂OCOCHCH)2)(CO)Fe 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:

: 65016-01-5
((CH₃OC₆H₄NCCH₃)2)(CO)3Fe

: 6032-74-2
diethyl (2E,4E)-2,4-hexadienedioate

: 82134-11-0
((CH₃OC₆H₄NCCH₃)2)((CH₃CH₂OCOCHCH)2)(CO)Fe

Guidance literature:: In acetone; Irradiation (UV/VIS); a soln. of a complex and of a ligand was irradiated for ca. 2 h with argon slow bubbling; not isolated, immediately used in the next step;

Reference yield:

: 108918-83-8
(η2-diethyl muconate){biacetyl bis(4-methoxyanil)}dicarbonyliron

: 82134-11-0
((CH₃OC₆H₄NCCH₃)2)((CH₃CH₂OCOCHCH)2)(CO)Fe

: 65016-01-5
((CH₃OC₆H₄NCCH₃)2)(CO)3Fe

Guidance literature:: In benzene; a partial disproportionation occurs on standing in soln.; products were not isolated; determined by IR spectra;

Reference yield: 74.0%

: 82134-11-0
((CH₃OC₆H₄NCCH₃)2)((CH₃CH₂OCOCHCH)2)(CO)Fe

: 108918-83-8
(η2-diethyl muconate){biacetyl bis(4-methoxyanil)}dicarbonyliron

Guidance literature:: With carbon monoxide; In acetone; a freshly prepd. soln. of monocarbonyl complex was continously flushed with CO; after additional stirring for 10 min under CO solvent was removed in vacuo; purified by crystallization from acetone; identified by IR and NMR spectra;