CAS 1271-42-7 Ferrocenecarboxylic acid - Catalysts / Alfa Chemistry

Synonyms

FERROENECARBOXYLIC ACID;CARBOXYFERROCENE;ferrocenemonocarboxylic acid;Ferrocenecarboxylic acid;FERROCENE,CARBOXY

IUPAC Name

Cyclopentadienecarboxylic acid ferrocenoic acid

Molecular Weight

230.04

Molecular Formula

C11H10FeO2

InChI Key

ZJYYFGVNIWNYII-UHFFFAOYSA-N

Boiling Point

236.7ºC at 760 mmHg

Melting Point

210ºC

Flash Point

104.2ºC

Purity

99%+

Solubility

Insoluble in water

Appearance

Yellow powder

Storage

Inert atmosphere, room temperature

EC Number

215-040-6

Exact Mass

230.00300

H-Bond Acceptor

H-Bond Donor

LogP

1.49530

MDL Number

MFCD00001430

Stability

Stable. Incompatible with strong oxidizing agents.

Vapor Pressure

0.016mmHg at 25°C

Application

Ferrocenecarboxylic acid serves as a versatile and highly valuable compound in various fields due to its unique structure, which connects two ferrocene molecules through a carboxy ligand. This metal-organic compound is not only stable but also exhibits high reactivity, making it a focal point of research for its applications in catalysis, materials science, and medicine. In catalysis, it plays the role of a catalyst, aiding in the synthesis of a wide array of compounds through polymerization, oxidation, and reduction reactions. In materials science, it acts as a fundamental building block for the creation of polymers and nanomaterials. Despite the ongoing exploration into its exact mechanism, it's thought that the carboxy ligand forms a stable complex with ferrocene, interacting with various molecules, including proteins, to facilitate numerous reactions. Additionally, Ferrocenecarboxylic acid is instrumental in the esterification of complex mixtures of phenols and alcohols for analysis via GCMS and serves as a crucial raw material and intermediate in organic synthesis, pharmaceuticals, agrochemicals, and dyestuffs.

January 18, 2025

Review Effective and Versatile Catalyst for Research Applications

Using Ferrocenecarboxylic acid in our research was transformative. It facilitated efficient catalysis in synthesizing polymers and nanomaterials. The stable yet reactive nature made our experiments smoother, especially in organic synthesis and analysis using GCMS.