Cas no 881040-54-6 (2-(2,5-Dimethylphenyl)imidazo1,2-apyridine-3-carbaldehyde)

2-(2,5-Dimethylphenyl)imidazo[1,2-a]pyridine-3-carbaldehyde is a versatile heterocyclic aldehyde with potential applications in pharmaceutical and organic synthesis. Its imidazopyridine core, combined with the dimethylphenyl substituent, offers structural rigidity and electronic modulation, making it a valuable intermediate for drug discovery and material science. The aldehyde functional group provides a reactive site for further derivatization, enabling the synthesis of diverse compounds such as Schiff bases or heterocyclic derivatives. This compound exhibits stability under standard conditions, ensuring consistent performance in synthetic workflows. Its well-defined molecular structure allows for precise control in reactions, supporting the development of novel bioactive molecules or functional materials.
2-(2,5-Dimethylphenyl)imidazo1,2-apyridine-3-carbaldehyde structure
881040-54-6 structure
Product Name:2-(2,5-Dimethylphenyl)imidazo1,2-apyridine-3-carbaldehyde
CAS No:881040-54-6
MF:C16H14N2O
MW:250.295163631439
MDL:MFCD05177278
CID:2128891
PubChem ID:4715285
Update Time:2025-05-20

2-(2,5-Dimethylphenyl)imidazo1,2-apyridine-3-carbaldehyde Chemical and Physical Properties

Names and Identifiers

    • 2-(2,5-Dimethylphenyl)imidazo[1,2-a]pyridine-3-carbaldehyde
    • LS-02440
    • MFCD05177278
    • 881040-54-6
    • AKOS000265983
    • CS-0326131
    • BBL022452
    • H24236
    • DB-354680
    • ALBB-006795
    • STK504122
    • 2-(2,5-Dimethylphenyl)imidazo1,2-apyridine-3-carbaldehyde
    • MDL： MFCD05177278
    • Inchi： 1S/C16H14N2O/c1-11-6-7-12(2)13(9-11)16-14(10-19)18-8-4-3-5-15(18)17-16/h3-10H,1-2H3
    • InChI Key： FKEJTILFXONHSM-UHFFFAOYSA-N
    • SMILES： O=CC1=C(C2C=C(C)C=CC=2C)N=C2C=CC=CN12

Computed Properties

  • Exact Mass: 250.110613074Da
  • Monoisotopic Mass: 250.110613074Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 2
  • Complexity: 333
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 3.9
  • Topological Polar Surface Area: 34.4?2

2-(2,5-Dimethylphenyl)imidazo1,2-apyridine-3-carbaldehyde Security Information

  • HazardClass：IRRITANT

2-(2,5-Dimethylphenyl)imidazo1,2-apyridine-3-carbaldehyde Pricemore >>

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2-(2,5-Dimethylphenyl)imidazo1,2-apyridine-3-carbaldehyde Related Literature

Additional information on 2-(2,5-Dimethylphenyl)imidazo1,2-apyridine-3-carbaldehyde

Comprehensive Overview of 2-(2,5-Dimethylphenyl)imidazo[1,2-a]pyridine-3-carbaldehyde (CAS No. 881040-54-6)

2-(2,5-Dimethylphenyl)imidazo[1,2-a]pyridine-3-carbaldehyde (CAS No. 881040-54-6) is a highly specialized organic compound that has garnered significant attention in pharmaceutical and materials science research. This compound belongs to the imidazo[1,2-a]pyridine family, a class of heterocyclic compounds known for their diverse biological activities and applications in drug discovery. The presence of the carbaldehyde functional group further enhances its reactivity, making it a valuable intermediate in synthetic chemistry.

In recent years, the demand for imidazo[1,2-a]pyridine derivatives has surged due to their potential therapeutic properties, including antimicrobial, anti-inflammatory, and anticancer effects. Researchers are particularly interested in 2-(2,5-Dimethylphenyl)imidazo[1,2-a]pyridine-3-carbaldehyde for its unique structural features, which allow for further functionalization and optimization. Its CAS No. 881040-54-6 serves as a critical identifier in chemical databases, ensuring accurate tracking and regulatory compliance.

The synthesis of 2-(2,5-Dimethylphenyl)imidazo[1,2-a]pyridine-3-carbaldehyde typically involves multi-step organic reactions, including condensation and oxidation processes. Advanced techniques such as microwave-assisted synthesis and catalyzed reactions have been explored to improve yield and efficiency. These innovations align with the growing trend toward green chemistry and sustainable practices in the chemical industry.

One of the most frequently asked questions about this compound revolves around its solubility and stability under various conditions. Studies indicate that 2-(2,5-Dimethylphenyl)imidazo[1,2-a]pyridine-3-carbaldehyde exhibits moderate solubility in polar organic solvents like dimethyl sulfoxide (DMSO) and methanol, while remaining stable at room temperature when stored properly. These properties make it suitable for laboratory-scale experiments and industrial applications.

Another area of interest is the compound's potential role in photovoltaic materials and organic electronics. The imidazo[1,2-a]pyridine core, combined with the carbaldehyde group, offers intriguing electronic properties that could be harnessed for developing next-generation optoelectronic devices. This aligns with the global push for renewable energy solutions and advanced materials.

From a regulatory perspective, CAS No. 881040-54-6 is not classified as a hazardous substance under major chemical safety frameworks. However, standard laboratory precautions, such as the use of personal protective equipment (PPE) and proper ventilation, are recommended when handling this compound. Its non-toxic profile and versatility make it a preferred choice for researchers exploring novel applications.

In summary, 2-(2,5-Dimethylphenyl)imidazo[1,2-a]pyridine-3-carbaldehyde (CAS No. 881040-54-6) represents a promising candidate for both pharmaceutical and materials science research. Its unique chemical structure, coupled with its broad applicability, positions it as a compound of significant interest in the scientific community. As research continues to uncover its full potential, this compound is likely to play a pivotal role in advancing innovation across multiple disciplines.

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