Cas no 2060029-03-8 (8-fluoro-1-methylisoquinoline-6-sulfonyl chloride)

8-Fluoro-1-methylisoquinoline-6-sulfonyl chloride is a specialized sulfonyl chloride derivative used primarily as a key intermediate in organic synthesis and pharmaceutical research. Its reactive sulfonyl chloride group enables efficient derivatization, making it valuable for constructing sulfonamides and other functionalized compounds. The fluorine substituent enhances electronic properties, influencing reactivity and binding interactions in target molecules. The methyl group at the 1-position contributes to steric and electronic modulation, improving selectivity in synthetic applications. This compound is particularly useful in medicinal chemistry for developing bioactive molecules due to its balanced reactivity and structural features. Proper handling under anhydrous conditions is recommended due to its moisture-sensitive nature.
8-fluoro-1-methylisoquinoline-6-sulfonyl chloride structure
2060029-03-8 structure
Product Name:8-fluoro-1-methylisoquinoline-6-sulfonyl chloride
CAS No:2060029-03-8
MF:C10H7ClFNO2S
MW:259.684483766556
MDL:MFCD30501184
CID:5193155
PubChem ID:125456833
Update Time:2025-05-21

8-fluoro-1-methylisoquinoline-6-sulfonyl chloride Chemical and Physical Properties

Names and Identifiers

    • 6-Isoquinolinesulfonyl chloride, 8-fluoro-1-methyl-
    • 8-fluoro-1-methylisoquinoline-6-sulfonyl chloride
    • MDL: MFCD30501184
    • Inchi: 1S/C10H7ClFNO2S/c1-6-10-7(2-3-13-6)4-8(5-9(10)12)16(11,14)15/h2-5H,1H3
    • InChI Key: HUOKCVHQYHSLOX-UHFFFAOYSA-N
    • SMILES: C1(C)C2=C(C=C(S(Cl)(=O)=O)C=C2F)C=CN=1

8-fluoro-1-methylisoquinoline-6-sulfonyl chloride Pricemore >>

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Additional information on 8-fluoro-1-methylisoquinoline-6-sulfonyl chloride

Research Brief on 8-Fluoro-1-methylisoquinoline-6-sulfonyl Chloride (CAS: 2060029-03-8): Recent Advances and Applications

8-Fluoro-1-methylisoquinoline-6-sulfonyl chloride (CAS: 2060029-03-8) is a specialized chemical compound that has garnered significant attention in the field of chemical biology and medicinal chemistry due to its versatile reactivity and potential applications in drug discovery and development. This sulfonyl chloride derivative serves as a key intermediate in the synthesis of biologically active molecules, particularly in the construction of sulfonamide-based compounds, which are widely utilized in pharmaceuticals for their diverse therapeutic properties.

Recent studies have highlighted the importance of 8-fluoro-1-methylisoquinoline-6-sulfonyl chloride in the development of novel enzyme inhibitors and receptor modulators. Its unique structural features, including the fluorine substitution and the sulfonyl chloride moiety, make it an attractive scaffold for designing compounds with enhanced binding affinity and selectivity. Researchers have employed this compound in the synthesis of targeted inhibitors for kinases, proteases, and other enzymes implicated in various diseases, such as cancer, inflammatory disorders, and infectious diseases.

One notable application of 8-fluoro-1-methylisoquinoline-6-sulfonyl chloride is in the development of fluorescent probes and imaging agents. The isoquinoline core, combined with the fluorine atom, provides favorable photophysical properties, enabling its use in bioimaging and diagnostic applications. Recent publications have demonstrated its utility in the design of turn-on fluorescent sensors for detecting specific biomolecules in cellular environments, offering new tools for studying disease mechanisms at the molecular level.

In addition to its role in medicinal chemistry, this compound has also been explored in materials science. Its sulfonyl chloride group allows for facile conjugation with polymers and other materials, making it a valuable building block for functionalized surfaces and nanomaterials. Researchers have utilized it to create advanced materials with applications in drug delivery, biosensing, and tissue engineering.

The synthesis and characterization of 8-fluoro-1-methylisoquinoline-6-sulfonyl chloride have been refined in recent years, with improvements in yield, purity, and scalability. Modern synthetic approaches, including microwave-assisted reactions and flow chemistry, have been employed to optimize its production, ensuring consistent quality for research and industrial applications. Analytical techniques such as NMR spectroscopy, mass spectrometry, and X-ray crystallography have been instrumental in confirming its structure and purity.

Future research directions for this compound include expanding its applications in targeted drug delivery systems and exploring its potential in combination therapies. The integration of computational modeling and high-throughput screening methods is expected to accelerate the discovery of new derivatives with enhanced pharmacological properties. Furthermore, ongoing studies aim to elucidate its mechanism of action in various biological systems, paving the way for innovative therapeutic strategies.

In conclusion, 8-fluoro-1-methylisoquinoline-6-sulfonyl chloride (CAS: 2060029-03-8) represents a promising chemical entity with broad applicability in chemical biology, medicinal chemistry, and materials science. Its continued exploration holds great potential for advancing drug discovery and developing cutting-edge technologies in the life sciences.

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