Cas no 941995-77-3 (N-4-(6-methoxypyridazin-3-yl)phenylnaphthalene-2-sulfonamide)

N-4-(6-methoxypyridazin-3-yl)phenylnaphthalene-2-sulfonamide structure
941995-77-3 structure
Product Name:N-4-(6-methoxypyridazin-3-yl)phenylnaphthalene-2-sulfonamide
CAS No:941995-77-3
MF:C21H17N3O3S
MW:391.442983388901
CID:5503393
Update Time:2025-10-29

N-4-(6-methoxypyridazin-3-yl)phenylnaphthalene-2-sulfonamide Chemical and Physical Properties

Names and Identifiers

    • 2-Naphthalenesulfonamide, N-[4-(6-methoxy-3-pyridazinyl)phenyl]-
    • N-4-(6-methoxypyridazin-3-yl)phenylnaphthalene-2-sulfonamide
    • Inchi: 1S/C21H17N3O3S/c1-27-21-13-12-20(22-23-21)16-6-9-18(10-7-16)24-28(25,26)19-11-8-15-4-2-3-5-17(15)14-19/h2-14,24H,1H3
    • InChI Key: FYJSPADPGWNAFS-UHFFFAOYSA-N
    • SMILES: C1=C2C(C=CC=C2)=CC=C1S(NC1=CC=C(C2=NN=C(OC)C=C2)C=C1)(=O)=O

N-4-(6-methoxypyridazin-3-yl)phenylnaphthalene-2-sulfonamide Pricemore >>

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Additional information on N-4-(6-methoxypyridazin-3-yl)phenylnaphthalene-2-sulfonamide

N-4-(6-methoxypyridazin-3-yl)phenylnaphthalene-2-sulfonamide: A Comprehensive Overview of Its Properties and Applications

N-4-(6-methoxypyridazin-3-yl)phenylnaphthalene-2-sulfonamide, with CAS number 941995-77-3, represents a sophisticated chemical entity in the realm of organic synthesis and pharmaceutical research. This compound, often abbreviated in discussions among researchers for its complex structure, integrates a naphthalene sulfonamide core with a methoxypyridazine-phenyl substituent, showcasing unique physicochemical attributes. Its molecular architecture, featuring both aromatic and heterocyclic components, contributes to its versatility in various scientific applications, particularly in drug discovery and material science. The growing interest in such compounds aligns with current trends in precision medicine and AI-driven molecular design, where researchers frequently search for "sulfonamide derivatives in cancer therapy" or "heterocyclic compounds for neurodegenerative diseases," highlighting its relevance in cutting-edge biomedical fields.

The chemical properties of N-4-(6-methoxypyridazin-3-yl)phenylnaphthalene-2-sulfonamide are characterized by its moderate solubility in polar organic solvents, a melting point typically above 200°C, and stability under standard laboratory conditions, making it suitable for experimental workflows. Its structure includes key functional groups such as the sulfonamide moiety, known for hydrogen bonding capabilities, and the methoxy group, which enhances electronic properties. These features are crucial for interactions in biological systems, often explored in queries like "sulfonamide bioactivity mechanisms" or "pyridazine derivatives solubility," reflecting user curiosity in pharmacokinetics and drug formulation. Additionally, its fluorescence properties, derived from the naphthalene core, position it as a candidate in biomarker development and diagnostic imaging, areas gaining traction due to advancements in non-invasive medical technologies.

In pharmaceutical applications, N-4-(6-methoxypyridazin-3-yl)phenylnaphthalene-2-sulfonamide is investigated for its potential as a kinase inhibitor or modulator in signaling pathways, with studies focusing on diseases like oncology and inflammation. This aligns with hot topics such as "targeted cancer therapies" and "personalized medicine," where users often search for "novel sulfonamide drugs 2024" or "kinase inhibitors side effects." Its design leverages the synergy between the naphthalene and pyridazine rings, offering insights into structure-activity relationships (SAR) that are pivotal in optimizing drug efficacy and reducing off-target effects. Moreover, the compound's role in high-throughput screening assays supports the trend toward automation in drug discovery, a subject frequently queried in contexts like "AI in chemical screening" or "automated lab workflows."

Beyond biomedicine, this compound finds utility in material science, particularly in the development of organic electronic devices such as OLEDs or sensors, due to its conjugated system and electronic properties. This application taps into user interests in "sustainable materials" and "green chemistry," with common searches including "organic semiconductors for energy efficiency" or "naphthalene-based materials." The integration of such compounds into renewable energy solutions underscores their importance in addressing global challenges like climate change, making them a focal point in interdisciplinary research. Furthermore, its stability and synthetic accessibility encourage explorations in catalysis and nanotechnology, areas where queries like "catalyst design using heterocycles" or "nanomaterial synthesis" are prevalent.

The synthesis of N-4-(6-methoxypyridazin-3-yl)phenylnaphthalene-2-sulfonamide typically involves multi-step organic reactions, starting from commercially available precursors like naphthalene-2-sulfonyl chloride and appropriately substituted anilines, followed by coupling with methoxypyridazine derivatives. This process emphasizes green chemistry principles, such as minimizing waste and using eco-friendly solvents, which resonates with current user concerns about "sustainable synthesis methods" and "environmental impact of chemicals." Researchers often search for "efficient sulfonamide synthesis" or "scalable heterocycle production," highlighting the demand for practical and scalable approaches. Optimizations in yield and purity are critical, driven by advancements in process chemistry and analytical techniques like HPLC and NMR spectroscopy.

Market dynamics and future prospects for N-4-(6-methoxypyridazin-3-yl)phenylnaphthalene-2-sulfonamide are shaped by its potential in emerging fields such as digital health and biotech innovations. With the rise of AI and machine learning in chemical research, this compound is part of a broader trend toward data-driven molecule design, addressing queries like "AI in drug discovery 2024" or "chemical databases for research." Its niche applications could lead to collaborations between academia and industry, fostering innovation in sectors like pharmaceuticals and electronics. As global focus shifts toward healthtech advancements and sustainable development, compounds like this are poised to play a role in next-generation technologies, making them a subject of ongoing interest and investment.

In conclusion, N-4-(6-methoxypyridazin-3-yl)phenylnaphthalene-2-sulfonamide (CAS 941995-77-3) exemplifies the intersection of chemistry, biology, and technology, offering diverse applications from drug development to material science. Its study not only addresses current user queries on topics like "heterocyclic compound benefits" or "sulfonamide applications" but also contributes to broader scientific discourse on innovation and sustainability. As research progresses, this compound may unlock new possibilities, reinforcing its status as a valuable entity in the scientific community and aligning with SEO trends that emphasize detailed, expert-driven content for professionals and enthusiasts alike.

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