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Ferrocenecarboxylic acid CAS:1271-42-7

Ferrocenecarboxylic acid is an organometallic compound that features a carboxylic acid (-COOH) group attached to the ferrocene framework, which consists of two cyclopentadienyl rings sandwiching a central iron atom. This unique structure imparts distinctive chemical properties and reactivity patterns, making it valuable in materials science, catalysis, and organic synthesis. Ferrocenecarboxylic acid exhibits notable electrochemical behavior due to its redox-active nature, contributing to its application in sensors and energy storage devices. Additionally, its ability to serve as a precursor for various derivatives enhances its significance in developing novel compounds for pharmaceutical and industrial purposes.


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Application and Effect:

Ferrocenecarboxylic acid (C11H10FeO2) is a prominent member of the organometallic chemistry field, characterized by the combination of a ferrocene moiety with a carboxylic acid functional group. The ferrocene structure consists of two cyclopentadienyl rings (C5H5) that are symmetrically bonded to a central iron (Fe2+) atom, creating a stable and highly symmetric compound known for its unique electronic and magnetic properties. The introduction of the carboxylic acid group at one of the cyclopentadienyl rings allows for enhanced solubility and facilitates further chemical modifications. One of the key attractions of ferrocenecarboxylic acid is its versatility in various synthetic applications. As a carboxylic acid, it can undergo typical reactions associated with this functional group, such as esterification and amidation, allowing the formation of a wide range of derivatives. These derivatives can be tailored to exhibit specific biological or physical properties, making them suitable for applications in pharmaceuticals, agrochemicals, and materials science. Moreover, ferrocenecarboxylic acid displays interesting electrochemical properties due to the presence of the iron center. It can participate in oxidation-reduction reactions, making it a potential candidate for use in electrochemical sensors and energy storage systems, such as batteries and supercapacitors. The redox activity of the ferrocene unit enables the compound to function effectively as an electron transfer agent, enhancing its performance in these applications. In recent years, research has also focused on the biocompatibility and potential therapeutic applications of ferrocenecarboxylic acid and its derivatives. Studies suggest that some ferrocenecarboxylic acid-based compounds could possess anticancer or antimicrobial activities, highlighting their relevance in drug discovery and development. The ability to modify the ferrocene core while maintaining the carboxylic acid functionality provides a promising avenue for creating novel therapeutic agents. Furthermore, ferrocenecarboxylic acid's distinctive structure allows it to interact with various biomolecules, facilitating its use in biological sensing applications. Its incorporation into polymeric materials can improve the material's mechanical properties while providing functionalities related to electronic conduction or catalytic activity. Overall, ferrocenecarboxylic acid represents a multifaceted compound with significant implications across multiple scientific disciplines. Its unique structural features, combined with its diverse reactivity and electrochemical properties, underscore its importance in ongoing research. As studies continue to uncover new applications and derivatives, ferrocenecarboxylic acid is poised to play a crucial role in advancing both fundamental and applied aspects of chemistry, particularly in areas like materials development, energy storage, and medicinal chemistry.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C11H10FeO210*
Assay 99%
Appearance white powder
CAS No.  1271-42-7
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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