CAS 12093-10-6
:Ferrocenecarboxaldehyde
Description:
Ferrocenecarboxaldehyde, with the CAS number 12093-10-6, is an organometallic compound that features a ferrocenyl group, which consists of a ferrocene moiety attached to a carboxaldehyde functional group. This compound exhibits unique characteristics due to the presence of the iron-containing ferrocene structure, which imparts stability and distinctive electronic properties. Ferrocenecarboxaldehyde is typically a solid at room temperature and is known for its reactivity, particularly in nucleophilic addition reactions due to the electrophilic nature of the aldehyde group. It can participate in various chemical transformations, making it a valuable intermediate in organic synthesis and materials science. The compound is also of interest in the field of coordination chemistry, where it can form complexes with various ligands. Additionally, ferrocenecarboxaldehyde may exhibit interesting electrochemical properties, which can be exploited in applications such as sensors and catalysis. Overall, its unique structure and reactivity make it a significant compound in both academic research and industrial applications.
Formula:C11H10FeO
InChI:InChI=1S/C6H5O.C5H5.Fe/c7-5-6-3-1-2-4-6;1-2-4-5-3-1;/h1-5H;1-5H;/q2*-1;+2
InChI key:InChIKey=MQHZGUNMWQBVDK-UHFFFAOYSA-N
SMILES:C(=O)[C-]12[Fe+2]3456789([CH]1=[CH]3[CH]4=[CH]52)[CH-]%10[CH]6=[CH]7[CH]8=[CH]9%10
Synonyms:- 1-Formylferrocene
- 2-Ferrocenecarboxaldehyde
- Cyclopenta-1,3-Diene
- Cyclopenta-2,4-Diene-1-Carbaldehyde
- Cyclopentadienecarboxaldehyde, cyclopentadienyliron deriv.
- Cyclopentadienyl(formylcyclopentadienyl)iron
- Ferrocencarbaldehyd
- Ferrocene Carboxyaldehyde
- Ferrocene, formyl-
- Ferrocene-1-carboxaldehyde
- Ferrocenealdehyde
- Ferrocenecarbaldehyde
- Ferrocenocarbaldehido
- Ferrocenylcarbaldehyde
- Ferrocenylcarboxaldehyde
- Formyldicyclopentadienyliron
- Formylferrocene
- Iron
- Iron(2+) Cyclopenta-2,4-Dienide Cyclopenta-2,4-Dien-1-Ylidenemethanolate (1:1:1)
- Iron, cyclopentadienyl(formylcyclopentadienyl)-
- Nsc 407052
- See more synonyms
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Found 7 products.
Ferrocenecarboxaldehyde
CAS:Formula:C11H10FeOPurity:>97.0%(GC)(T)Color and Shape:Light yellow to Brown powder to crystalMolecular weight:214.05Ferrocenecarboxaldehyde, 97%
CAS:<p>Ferrocenecarboxaldehyde, is used to prepare chiral ferrocene aziridinylmethanols for selective azomethine ylide cycloaddtion. It is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals. This Thermo Scientific Chemicals brand product was originally par</p>Formula:C11H10FeOPurity:97%Color and Shape:Powder or crystals or crystalline powderMolecular weight:214.05Ferrocene carboxaldehyde, min. 98%
CAS:<p>Ferrocene carboxaldehyde, min. 98%</p>Formula:H(O)CC5H4FeC5H5Purity:min. 98%Color and Shape:orange to red xtl.Molecular weight:214.05Cyclopentadienyl(formylcyclopentadienyl)iron
CAS:Formula:C11H20FeOPurity:97%Color and Shape:LiquidMolecular weight:224.1209Ferrocenecarboxaldehyde
CAS:<p>Ferrocenecarboxaldehyde</p>Formula:C11H10FeOPurity:98%Color and Shape: brown solidMolecular weight:214.04g/molFerrocenecarboxaldehyde
CAS:Formula:C11H10FeOPurity:95%Color and Shape:Crystalline PowderMolecular weight:214.045Ferrocenecarboxaldehyde
CAS:<p>Ferrocenecarboxaldehyde is a fatty acid with a ferrocene carboxylic acid group. It has been shown to have antimicrobial activity against bacteria, fungi, and yeast when it was mixed with nitric acid. Ferrocenecarboxaldehyde can be synthesized by reacting ferrocene with glycerol in the presence of sulfuric acid. The reaction mechanism of this synthesis is as follows: The structural analysis of ferrocenecarboxaldehyde has been studied using FT-IR spectroscopy and NMR spectroscopy. The chemical structure of ferrocenecarboxaldehyde is as follows: The asymmetric synthesis of ferrocenecarboxaldehyde is shown below:</p>Formula:C11H10FeOPurity:Min. 95%Color and Shape:PowderMolecular weight:214.04 g/mol






