Cas no 55655-84-0 (1-3-(Trifluoromethyl)phenylbutane-1,3-dione)

1-3-(Trifluoromethyl)phenylbutane-1,3-dione is a fluorinated β-diketone compound characterized by its trifluoromethyl-substituted phenyl group. This structural feature enhances its electron-withdrawing properties, making it a valuable intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and coordination chemistry. The presence of the trifluoromethyl group improves thermal stability and reactivity, facilitating its use in cross-coupling reactions and as a ligand precursor for metal complexes. Its high purity and well-defined structure ensure consistent performance in research and industrial applications. The compound is particularly useful in pharmaceuticals, agrochemicals, and materials science due to its ability to introduce fluorinated motifs into target molecules.
1-3-(Trifluoromethyl)phenylbutane-1,3-dione structure
55655-84-0 structure
Product Name:1-3-(Trifluoromethyl)phenylbutane-1,3-dione
CAS No:55655-84-0
MF:C11H9F3O2
MW:230.183173894882
CID:870543
Update Time:2026-04-29

1-3-(Trifluoromethyl)phenylbutane-1,3-dione Chemical and Physical Properties

Names and Identifiers

    • 1-(3-TRIFLUOROMETHYL-PHENYL)-BUTANE-1,3-DIONE
    • 1-(3-trifluoromethylphenyl)butane-1,3-dione
    • AG-F-94779
    • CTK1G8429
    • KB-214045
    • SureCN9536997
    • 1-3-(Trifluoromethyl)phenylbutane-1,3-dione

Computed Properties

  • Exact Mass: 230.05547

Experimental Properties

  • PSA: 34.14

1-3-(Trifluoromethyl)phenylbutane-1,3-dione Pricemore >>

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Additional information on 1-3-(Trifluoromethyl)phenylbutane-1,3-dione

Comprehensive Overview of 1-3-(Trifluoromethyl)phenylbutane-1,3-dione (CAS No. 55655-84-0)

1-3-(Trifluoromethyl)phenylbutane-1,3-dione (CAS No. 55655-84-0) is a specialized organic compound widely recognized for its unique structural and functional properties. This diketone derivative, featuring a trifluoromethylphenyl group, has garnered significant attention in pharmaceutical, agrochemical, and material science research. Its molecular formula, C11H9F3O2, highlights its potential as a versatile intermediate in synthetic chemistry. Researchers and industries are increasingly exploring its applications due to its stability, reactivity, and compatibility with various chemical processes.

The compound's trifluoromethyl moiety is particularly noteworthy, as it enhances lipophilicity and metabolic stability—key traits in drug design. This aligns with current trends in fluorinated compound research, a hot topic in medicinal chemistry. With the rise of AI-driven drug discovery, tools like molecular docking and QSAR modeling frequently utilize such compounds to predict bioactivity. Searches for "fluorinated diketones in drug development" or "CAS 55655-84-0 applications" reflect growing interest in this niche.

From a synthetic perspective, 1-3-(Trifluoromethyl)phenylbutane-1,3-dione serves as a precursor for heterocyclic frameworks, including pyrazoles and isoxazoles. These scaffolds are pivotal in designing biologically active molecules, addressing global demand for novel therapeutics. Recent publications emphasize its role in green chemistry initiatives, where solvent-free reactions and catalytic methods are prioritized. Queries like "sustainable synthesis of fluorinated diketones" underscore this shift toward eco-friendly methodologies.

In material science, the compound's conjugated diketone system enables applications in organic electronics, such as OLEDs and photovoltaic cells. Its ability to coordinate with metal ions also makes it valuable for luminescent materials—a trending area tied to renewable energy solutions. SEO analytics reveal spikes in searches for "diketone-based optoelectronic materials," indicating cross-disciplinary relevance.

Quality control of CAS No. 55655-84-0 relies on advanced analytical techniques like HPLC, NMR, and mass spectrometry, ensuring purity for high-end applications. Regulatory compliance with REACH and FDA guidelines further solidifies its commercial viability. Frequently asked questions, such as "how to characterize trifluoromethylphenyl diketones," highlight the need for accessible technical data.

In summary, 1-3-(Trifluoromethyl)phenylbutane-1,3-dione exemplifies the convergence of innovation and practicality. Its multifaceted utility—from drug discovery to advanced materials—positions it as a compound of enduring scientific and industrial significance.

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