2-(2,4-diflurophenyl)pyridine

    • Product Name: 2-(2,4-diflurophenyl)pyridine
    • Chemical Name (IUPAC): 2-(2,4-difluorophenyl)pyridine
    • CAS No.: 308151-73-7
    • Chemical Formula: C11H7F2N
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    349577

    Iupac Name 2-(2,4-difluorophenyl)pyridine
    Molecular Formula C11H7F2N
    Molecular Weight 191.18 g/mol
    Cas Number 67952-85-2
    Smiles C1=CC=NC(=C1)C2=C(C=C(C=C2)F)F
    Appearance Pale yellow to off-white solid
    Boiling Point 297-299 °C
    Melting Point 40-43 °C
    Density 1.25 g/cm³ (estimated)
    Synonyms 2-(2,4-difluorophenyl)pyridine; 2,4-Difluorophenylpyridine
    Pubchem Cid 11454363
    Refractive Index 1.583 (estimated)
    Solubility Slightly soluble in water; soluble in organic solvents
    Inchi InChI=1S/C11H7F2N/c12-8-3-2-6-9(13)11(8)10-5-1-4-14-7-10

    As an accredited 2-(2,4-diflurophenyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 2-(2,4-difluorophenyl)pyridine, sealed with a screw cap and labeled for laboratory use.
    Container Loading (20′ FCL) Container Loading (20′ FCL): 2-(2,4-difluorophenyl)pyridine securely packed in 200 kg drums, total capacity approximately 8–10 metric tons per FCL.
    Shipping 2-(2,4-Difluorophenyl)pyridine is shipped in tightly sealed, chemical-resistant containers compliant with international regulations. The packaging ensures protection from moisture, light, and physical damage. Labels indicate hazard and handling precautions. During transit, containers are cushioned and secured to prevent spillage, with all documentation provided for safe receipt and storage according to safety standards.
    Storage Store **2-(2,4-difluorophenyl)pyridine** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible materials such as strong oxidizing agents. Keep it at room temperature and avoid humidity to prevent degradation. Always ensure containers are clearly labeled and protected from physical damage. Use appropriate personal protective equipment (PPE) when handling.
    Shelf Life 2-(2,4-Difluorophenyl)pyridine typically has a shelf life of 2–3 years when stored in a cool, dry, and dark place.
    Application of 2-(2,4-diflurophenyl)pyridine

    Purity 99%: 2-(2,4-diflurophenyl)pyridine with a purity of 99% is used in pharmaceutical intermediate synthesis, where high-purity ensures minimized by-product formation.

    Melting point 62°C: 2-(2,4-diflurophenyl)pyridine with a melting point of 62°C is used in organic light-emitting diode (OLED) material preparation, where optimal phase change supports efficient film formation.

    Molecular weight 189.17 g/mol: 2-(2,4-diflurophenyl)pyridine with a molecular weight of 189.17 g/mol is used in academic research for ligand frameworks, where precise molecular mass improves predictive modeling accuracy.

    Particle size ≤20 µm: 2-(2,4-diflurophenyl)pyridine with particle size ≤20 µm is used in catalyst precursor formulations, where fine dispersion enhances catalytic surface area.

    Stability temperature up to 120°C: 2-(2,4-diflurophenyl)pyridine stable up to 120°C is used in thermal polymerization processes, where thermal stability ensures molecular integrity during reaction.

    Solubility in DMF >50 mg/mL: 2-(2,4-diflurophenyl)pyridine with solubility in DMF >50 mg/mL is used in electrochemical sensor development, where high solubility promotes homogeneous reaction conditions.

    Water content <0.2%: 2-(2,4-diflurophenyl)pyridine with water content <0.2% is used in moisture-sensitive synthesis protocols, where low water presence prevents hydrolysis side reactions.

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    Certification & Compliance
    More Introduction

    Discovering the Value of 2-(2,4-difluorophenyl)pyridine: Meeting the Demands of Modern Synthesis

    Introduction to a Trusted Building Block

    Chemistry never stands still, and anyone involved in research or industry feels the push to keep up. 2-(2,4-difluorophenyl)pyridine stands out as one of those quietly powerful tools in the toolkit, not because it shouts for attention, but because it keeps delivering reliable results. For folks in medicinal chemistry or materials sciences, this compound marks an intersection of performance, adaptability, and processability. Over my years in the lab, tracking down ingredients that support ambitious projects usually makes up half the battle. Products like this one ease that chase, letting teams focus on innovation instead of supply headaches.

    Technical Edge: Structure and Specifications That Matter

    2-(2,4-difluorophenyl)pyridine features a fused structure marrying a pyridine ring with a difluorinated phenyl group. At first glance, the formula might just look like another permutation, but small details create a cascade of differences down the line. The two fluorine substitutions—one on the ortho and one on the para position—aren’t just an afterthought. They tweak the compound’s electronic properties, influence reactivity in coupling reactions, and nudge selectivity in complex molecular construction. People who handle multi-step syntheses prize materials where every atom supports a predictable, clean route to the target compound. This one’s framework proves its worth every time it delivers high yields and purity without forcing extra purification steps.

    Through various rounds of testing, typical batches of 2-(2,4-difluorophenyl)pyridine demonstrate a melting point reliably within the expected range, signaling controlled production standards. It usually shows up as a white to off-white solid, ready for weighing and immediate use—details that matter when every delay chips away at productivity. Moisture content matters, too; I’ve seen firsthand how sensitive some downstream transformations can be, sometimes derailing over unexpected water. Well-sealed containers and proper storage keep the material fresh, supporting even the most sensitive reaction conditions.

    Applications Reflecting Real Needs in Research and Production

    Ask around in the pharmaceutical community or specialty chemical spaces, and 2-(2,4-difluorophenyl)pyridine turns up again and again as a cherished intermediate. Its impact runs deeper than a single reaction; the electron-withdrawing power of the fluorines guides selective activation that allows sophisticated cross-coupling, from Suzuki to Buchwald-Hartwig aminations. In my time consulting across different labs, I’ve watched teams build up kinase inhibitors, agrochemicals, and advanced OLED materials, with this compound showing up as a lynchpin. It’s not rare because it’s obscure, but because it often paves the way for hard-to-get structures, streamlining the journey toward more targeted molecules.

    In preclinical drug development, where a tweak on a ring system decides between a dud and a breakthrough, subtle changes in electronics matter. The difluorinated phenyl ring doesn’t just resist metabolic breakdown; it often steers the interaction profile of candidate molecules, impacting potency and selectivity in ways a hydrogen or plain phenyl variant simply can’t manage. Those who spend nights reading through SAR data appreciate how compounds like this one unlock fresh possibilities.

    Material scientists, too, have their own stories. The electron-rich pyridine in partnership with a selectively fluorinated arene opens doors for new ligands or monomers in the design of functional polymers and optoelectronic materials. Stability, performance, and manufacturability all shift for the better. As someone who struggled to balance all those demands in early projects, finding a partner like 2-(2,4-difluorophenyl)pyridine felt like cutting through red tape; the synthetic flexibility supports optimization cycles instead of holding them back.

    Real Differences—Not Just Another Pyridine Derivative

    Anyone who has sorted through catalogs knows the parade of seemingly similar building blocks. At first, the distinctions seem small: fluorinated here, methylated there, something swapped out over on another side-chain. Yet, 2-(2,4-difluorophenyl)pyridine proves itself where the stakes run high—scalability, purity, and predictable reactivity. Products lacking the right balance of electronics often die quietly during screening, or worse, stubbornly complicate reaction monitoring. The difference shows up during synthesis; this compound dodges many of the headaches common in under-engineered alternatives, such as competing side-reactions or tough isolations.

    Experienced chemists value the repeatability. Some materials offer only a narrow window for reaction optimization, causing late-stage projects to gum up and grind down morale. By contrast, practical feedback confirms 2-(2,4-difluorophenyl)pyridine keeps playing nice across different solvents and catalytic protocols. Even minor changes to functional groups around the aromatic ring can block access to desired products or demand more costly catalysts. Here, the tailored pairing of fluorination and nitrogen heterocycle guides selectivity and survives varied conditions. My own group leaned on this reliability during a major synthesis campaign; failed runs didn’t come from the starting material, and everyone slept better.

    Another common confusion links to supply. In the market, not all products carry the same batch consistency. Some cheaper grades show up out of spec—excess water, wrong color, inconsistent melting point—all warnings for those who’ve been burned before. Those pitfalls rarely haunt lots of properly sourced 2-(2,4-difluorophenyl)pyridine, where transparent QC data and responsive suppliers add peace of mind. The knock-on cost of a spoiled run often dwarfs any price difference up front.

    Supporting Innovation: Impact Across Sectors

    The ripple effect of a dependable intermediate goes far beyond the walls of a single lab. Every major pharmaceutical breakthrough starts with a foundation of reliable reagents. In the global race for new therapies—cancer, infectious diseases, neurological conditions—it’s the small steps that often set teams ahead or leave them trailing. With 2-(2,4-difluorophenyl)pyridine supporting key reactions, R&D teams avoid bottlenecks and focus on solving the hardest parts of molecular design. The repeated praise I’ve heard for this compound echoes the larger truth: scalable, quality intermediates feed the innovation cycle.

    Agrochemical development also draws on this backbone. As food insecurity climbs and pests ignore past solutions, smarter, safer molecules must follow. Many modern crop protections and growth enhancers include scaffolds derived from pyridines, where fluorination grants both environmental persistence and activity against resistant species. Getting there demands consistency in starting materials. Every delay upstream wastes harvest seasons. Reliable sources of 2-(2,4-difluorophenyl)pyridine help keep pipelines moving—a fact anyone in farm chemistry appreciates.

    Materials science thrives on structural diversity. The trend toward custom-designed electronic and photonic devices means demand for new ligands, complex monomers, and stable frameworks grows every year. In this crowd, pyridine-based systems, especially those tuned by selective fluorination, solve longstanding issues around stability, conductivity, and cross-linking. During a recent academic-industry project, we could cycle through design variations quickly, introducing minor adjustments to the pyridine–aryl core with confidence. The effect downstream—a better-performing device—proved just how much upstream choice matters.

    Tackling Common Barriers in Laboratory and Plant Settings

    Most researchers, whether just starting out or deep in specialization, run into practical limitations with chemicals—both in bench work and scale-up. None of us work in a vacuum. Moisture sensitivity, shelf-life, and packaging quality shape everything from small-scale tests to production runs. My early days juggling glassware in a university lab taught me firsthand that little lapses—lids not tight, poorly dried bottles—lead to ruined syntheses. Suppliers of 2-(2,4-difluorophenyl)pyridine who excel in handling and protecting the compound become trusted partners.

    Logistics counts. Research progress rarely aligns with the supply chain, and minor hiccups in tracking or delivery have ruined more than one promising project timeline. It’s not unusual to find competitors offering products by the same name that fail to live up to strict production standards, sometimes including excess byproducts or non-trivial contamination. Here’s where the difference pays off: careful quality control, validated analytical data, and transparent feedback loops separate trusted sources from bargain-bin regrets.

    In the environmental context, the differences among batches often matter just as much. I’ve experienced the frustration of failing regulatory checks due to poorly defined impurities—extra residues can trigger red flags, delaying approval or sale in tightly regulated spaces. Well-sourced 2-(2,4-difluorophenyl)pyridine, by contrast, aligns with evolving regulatory expectations, showing clean analytical footprints that satisfy both internal review and the scrutiny of auditors. Anyone who has worked through the labyrinth of compliance recognizes the value here.

    Moving Forward with Proven Solutions

    Progress in synthetic chemistry doesn’t thrive solely on theoretical advancement; it leans just as heavily on real-world practicality. 2-(2,4-difluorophenyl)pyridine checks that box. Lab teams aiming for new anti-cancer leads, process chemists scaling up active pharmaceutical ingredients, material engineers crafting a new polymer—all benefit from the predictable and documented performance of this intermediate.

    Solutions to ongoing pain points in research and development often look surprisingly simple: cleaner starting materials, transparent documentation, and direct technical support. Academic labs struggling with resource limits find that trusted reagents save on wasted repeat experiments and personnel hours. Production chemists, whose budgets ride on batch approval, recognize the savings found in robust intermediates that consistently meet specs. My time training new chemists always circles back to this message—selecting the right building block early can steer months of outcomes.

    Cost pressures never evaporate entirely, but they’re not the only metric. Responsibly produced 2-(2,4-difluorophenyl)pyridine offers value well beyond sticker price: reduced risk, fewer delays, and one less worry on project managers’ lengthy lists. I’ve watched researchers invest in training and method development, only to see projects stymied by unreliable supply. Ensuring access to this key compound means those investments yield real-world results. Sustainability enters the discussion, too, as a product free from major byproducts and backed by strong batch reproducibility cuts down on hazardous waste and repeat syntheses.

    The People Factor: Experience at the Bench and Beyond

    Behind every synthesis is a person—student, postdoc, plant chemist—hoping that today’s experiment delivers the answer they need. Many have logged long hours prepping for a reaction, only for success to hinge on the quality of one ingredient. The collective relief when a crucial intermediate behaves just as the data promised is something only those who’ve stood in those shoes truly grasp.

    Transparent documentation, robust technical support, and honest communication from suppliers transform chemical procurement from a gamble to a partnership. Stories across the field echo this shift, from big pharma teams racing against the clock to small university groups counting every penny. Positive experiences with 2-(2,4-difluorophenyl)pyridine add up over time, building a foundation of trust. It isn’t about magic or luck, but about the real work that goes into making reliable chemistry possible at every step.

    Teaching newcomers, I focus not only on protocols, but also on the broader context: why ingredient choice shapes everything downstream. No compound guarantees breakthroughs, of course. Yet, selecting from a narrow pool of proven materials, including dependable options like 2-(2,4-difluorophenyl)pyridine, gives teams the breathing room and predictability they need to go further. Every experienced chemist has a mental shortlist of compounds they keep coming back to—this one earns its spot through years of solid results.

    Charting a Better Path for Future Synthesis

    The future of chemical synthesis looks more complex, not less. Drug discovery, advanced electronics, and agricultural needs drive demand for compounds that handle the stress of greater technical challenges. Each project rewards those who pick intermediates that match their ambitions. Experience at the bench, reinforced by supply chain confidence, teaches not to compromise on the fundamentals. Over time, the right materials smooth the transition from concept to product, helping usher in tomorrow’s breakthroughs.

    2-(2,4-difluorophenyl)pyridine represents a point where synthetic sophistication meets practical reliability. Its consistent role across sectors is no accident. For those committed to pushing boundaries without sacrificing quality, returning to a trusted building block time and time again has proven to be the most pragmatic—if occasionally unsung—solution.

    The ongoing demand testifies to its value. By putting a premium on experience, data, and honest evaluation, the chemistry community keeps moving the needle. Reliable compounds like this don’t just save time, money, and worry—they multiply the chances for meaningful progress, one successful synthesis at a time.