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(η5-C5H5)Fe(CO)(PPh3)COCH2SePh

Base Information Edit
  • Chemical Name:(η5-C5H5)Fe(CO)(PPh3)COCH2SePh
  • CAS No.:827341-87-7
  • Molecular Formula:C32H27FeO2PSe
  • Molecular Weight:609.346
  • Hs Code.:
  • Mol file:827341-87-7.mol
(η5-C5H5)Fe(CO)(PPh3)COCH2SePh

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Chemical Property of (η5-C5H5)Fe(CO)(PPh3)COCH2SePh Edit
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Technology Process of (η5-C5H5)Fe(CO)(PPh3)COCH2SePh

There total 1 articles about (η5-C5H5)Fe(CO)(PPh3)COCH2SePh 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 n-butyllithium; In tetrahydrofuran; hexane; ubder N2 atm. to soln. Fe complex in THF at -78°C n-BuLi in hexane was added, after 2 h soln. PhSeSePh in THF was added and stirred for 1h; MeOH was added, react. mixt. was warmed to room temp., concd. in vacuo, residue was extd. with CH2Cl2, filtered through alumina V, filtrate was evapd., residue was purified by chromy. on silica (Et2O-pet.ether), crystn. from CH2Cl2-hexane; elem. anal.;
DOI:10.1016/j.jorganchem.2004.04.046
Guidance literature:
With n-butyllithium; In tetrahydrofuran; hexane; under N2 atm. to soln. Fe complex in THF acid at -78°C n-BuLi in hexane was added, allyl iodide was added after 2 h, react. mixt. was allowed to warm to room temp. over 16 h; soln. was concd. in vacuo, residue was extd. with CH2Cl2 and filtered through alumina V, solvent was removed, chromy. on silica (Et2O-pet.ether)and crystn. from CH2Cl2-hexane; elem. anal.;
DOI:10.1016/j.jorganchem.2004.04.046
Guidance literature:
With n-butyllithium; In tetrahydrofuran; hexane; ubder N2 atm. to soln. Fe complex in THF at -78°C n-BuLi in hexane was added, after 1 h MeI was added, allowed to warm to room temp. and stirred for 4 h; solvent was removed in vacuo, residue was extd. with CH2Cl2 and filteredthrough alumina V, filtrate was concd., residue was purified by chromy. on alumina; diastereomers were not separated;
DOI:10.1016/j.jorganchem.2004.04.046
upstream raw materials:

diphenyl diselenide

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