Aminoferrocene, with the CAS number 1273-82-1, is an organometallic compound that features a ferrocene structure, which consists of a central iron atom sandwiched between two cyclopentadienyl anions. The distinguishing characteristic of aminoferrocene is the presence of an amino group (-NH2) attached to one of the cyclopentadienyl rings, which imparts unique chemical properties. This compound is typically characterized by its stability, solubility in organic solvents, and its ability to undergo redox reactions, making it of interest in various applications, including electrochemistry and materials science. The amino group can participate in hydrogen bonding and can also serve as a site for further chemical modifications. Additionally, aminoferrocene can exhibit interesting electronic properties due to the interaction between the iron center and the amino group, which can influence its reactivity and potential use in drug delivery systems or as a catalyst in organic reactions. Overall, aminoferrocene is a versatile compound with significant implications in both theoretical and applied chemistry.

Aminoferrocene

Aminoferrocene is a redox active molecule that is used for biological studies. It has been shown to be synthesized by reacting trifluoroacetic acid and methanol in the presence of ferrocenecarboxylic acid. Aminoferrocene is a member of the group p2 of organometallic compounds with an electron-rich carbon atom. Aminoferrocene has been shown to bind to mitochondrial membranes, which may be due to its ability to interact with hydrogen bonding interactions, as well as its chemical stability. The reaction mechanism for aminoferrocene is not yet known, but it has been proposed that it may involve intramolecular hydrogen transfer or protonation.

CAS 1273-82-1: Aminoferrocene

Aminoferrocene

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Aminoferrocene

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Aminoferrocene

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Aminoferrocene

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Ferrocene, amino-

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