Cas no 1352898-81-7 (6-bromo-5-chloroimidazo[1,2-a]pyridine)

6-Bromo-5-chloroimidazo[1,2-a]pyridine is a halogenated heterocyclic compound featuring a fused imidazo[1,2-a]pyridine core. Its bromo and chloro substituents enhance reactivity, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. The electron-withdrawing effects of the halogens facilitate further functionalization, such as cross-coupling reactions, enabling the construction of complex molecular architectures. This compound exhibits high purity and stability under standard conditions, ensuring reliable performance in synthetic applications. Its structural versatility allows for modifications at multiple sites, supporting diverse research and industrial applications, including drug discovery and material science. Proper handling and storage are recommended due to its halogenated nature.
6-bromo-5-chloroimidazo[1,2-a]pyridine structure
1352898-81-7 structure
Product Name:6-bromo-5-chloroimidazo[1,2-a]pyridine
CAS No:1352898-81-7
MF:C7H4BrClN2
MW:231.477059364319
MDL:MFCD22552935
CID:2182787
PubChem ID:74890118
Update Time:2025-05-20

6-bromo-5-chloroimidazo[1,2-a]pyridine Chemical and Physical Properties

Names and Identifiers

    • 6-Bromo-5-chloro-imidazo[1,2-a]pyridine
    • 6-bromo-5-chloroimidazo[1,2-a]pyridine
    • P16141
    • AKOS023402523
    • CEC89881
    • AS-53157
    • DB-263818
    • SY042506
    • CS-0050263
    • MFCD22552935
    • SB21333
    • IMidazo[1,2-a]pyridine, 6-broMo-5-chloro-
    • 1352898-81-7
    • SCHEMBL18319487
    • MDL： MFCD22552935
    • Inchi： 1S/C7H4BrClN2/c8-5-1-2-6-10-3-4-11(6)7(5)9/h1-4H
    • InChI Key： STOHYIMQKKNYNR-UHFFFAOYSA-N
    • SMILES： BrC1C=CC2=NC=CN2C=1Cl

Computed Properties

  • Exact Mass: 229.92464g/mol
  • Monoisotopic Mass: 229.92464g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 0
  • Complexity: 155
  • 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: 3.4
  • Topological Polar Surface Area: 17.3?2

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6-bromo-5-chloroimidazo[1,2-a]pyridine Related Literature

Additional information on 6-bromo-5-chloroimidazo[1,2-a]pyridine

Comprehensive Overview of 6-bromo-5-chloroimidazo[1,2-a]pyridine (CAS No. 1352898-81-7): Properties, Applications, and Industry Insights

6-bromo-5-chloroimidazo[1,2-a]pyridine (CAS No. 1352898-81-7) is a heterocyclic organic compound that has garnered significant attention in pharmaceutical and agrochemical research. This imidazo[1,2-a]pyridine derivative is characterized by its unique bromo and chloro substituents, which enhance its reactivity and make it a valuable intermediate in synthetic chemistry. Researchers and industry professionals frequently search for terms like "6-bromo-5-chloroimidazo[1,2-a]pyridine synthesis," "CAS 1352898-81-7 applications," and "imidazo[1,2-a]pyridine derivatives," reflecting its growing relevance in drug discovery and material science.

The structural framework of 6-bromo-5-chloroimidazo[1,2-a]pyridine offers versatile functionalization opportunities, making it a key building block for designing bioactive molecules. Recent trends in AI-driven drug discovery and green chemistry have further amplified interest in such compounds, as they align with the demand for sustainable and efficient synthetic routes. Searches for "eco-friendly synthesis of halogenated imidazopyridines" and "computational modeling of CAS 1352898-81-7" highlight the intersection of this compound with cutting-edge scientific advancements.

In pharmaceutical applications, 6-bromo-5-chloroimidazo[1,2-a]pyridine serves as a precursor for developing kinase inhibitors and antimicrobial agents. Its halogenated imidazo[1,2-a]pyridine core is particularly attractive for modulating drug-target interactions, a topic frequently explored in "structure-activity relationship (SAR) studies." The compound's role in addressing antibiotic resistance and cancer therapeutics aligns with global health priorities, driving its prominence in academic and industrial research.

From a commercial perspective, the demand for CAS 1352898-81-7 is influenced by its scalability and purity standards. Suppliers and manufacturers often encounter queries like "high-purity 6-bromo-5-chloroimidazo[1,2-a]pyridine suppliers" or "cost-effective synthesis routes," underscoring the need for reliable production protocols. Analytical techniques such as HPLC and NMR are critical for quality control, ensuring compliance with regulatory requirements for pharmaceutical intermediates.

Looking ahead, the compound's potential extends to material science, where its electronic properties are explored for organic semiconductors and light-emitting diodes (OLEDs). This multidisciplinary appeal positions 6-bromo-5-chloroimidazo[1,2-a]pyridine as a compound of enduring interest, bridging gaps between chemistry, biology, and engineering. As research continues to uncover new applications, its role in precision medicine and sustainable technologies will likely expand, reinforcing its status as a cornerstone of modern synthetic chemistry.

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