C₆H₅C(O)NHC₂₅H₄₃N₅O₈^(3-)*Fe⁽³⁺⁾=C₆H₅C(O)NHC₂₅H₄₃FeN₅O₈

Base Information

• Chemical Name: C₆H₅C(O)NHC₂₅H₄₃N₅O₈^(3-)*Fe⁽³⁺⁾=C₆H₅C(O)NHC₂₅H₄₃FeN₅O₈
• CAS No.: 20446-16-6
• Molecular Formula: C₃₂H₄₉N₆O₉*Fe
• Molecular Weight: 717.623
• Mol file: 20446-16-6.mol

Synonyms:

Chemical Property of C₆H₅C(O)NHC₂₅H₄₃N₅O₈^(3-)*Fe⁽³⁺⁾=C₆H₅C(O)NHC₂₅H₄₃FeN₅O₈

Chemical Property:

Purity/Quality:

Safty Information:

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MSDS Files:

Useful:

Technology Process of C₆H₅C(O)NHC₂₅H₄₃N₅O₈^(3-)*Fe⁽³⁺⁾=C₆H₅C(O)NHC₂₅H₄₃FeN₅O₈

There total 1 articles about C₆H₅C(O)NHC₂₅H₄₃N₅O₈^(3-)*Fe⁽³⁺⁾=C₆H₅C(O)NHC₂₅H₄₃FeN₅O₈ 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: 90.0%

benzoylamide deferoxamine (105185-40-8) + iron(III) chloride (7705-08-0) → C6H5C(O)NHC25H43N5O8(3-)*Fe(3+)=C6H5C(O)NHC25H43FeN5O8 (20446-16-6)

Guidance literature:

In ethanol; byproducts: H(1+); Mixing of equimolar amt. of alcoholic soln. of starting materials and maintaining with slight boiling of solvent for 1 hr.; Evapn. of solvent at reduced pressure, drying of residue in vac. over P2O5, washing of obtained salt with dry ether from unreacted FeCl3, dissolving of dried material in MeOH, pptg. (dry ether), filtn. of ppt. and drying (vac., P2O5). Elem. anal.;

upstream raw materials:

benzoylamide deferoxamine

iron(III) chloride

Refernces