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2-Bromo-4-Phenylpyridine

    • Product Name 2-Bromo-4-Phenylpyridine
    • Alias 2-Bromo-4-phenylpyridine
    • Einecs 841-524-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
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    Specifications

    HS Code

    759540

    Cas Number 118716-01-9
    Molecular Formula C11H8BrN
    Molecular Weight 234.09 g/mol
    Appearance Off-white to light yellow solid
    Melting Point 71-74°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents (e.g., DMSO, dichloromethane)
    Smiles Brc1cc(ncc1)c2ccccc2
    Inchi InChI=1S/C11H8BrN/c12-10-7-9(8-13-11(10)6-5-3-1-2-4-6)8-9
    Storage Conditions Store at room temperature, tightly sealed

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    More Introduction

    Exploring the Impact of 2-Bromo-4-Phenylpyridine in Modern Chemistry

    Breaking Down the Basics

    Chemists and researchers ask a lot of their reagents. They need flexibility in synthesis, reliable purity, and clear advantages over similar chemicals. 2-Bromo-4-Phenylpyridine stands out to many of us not because it makes bold claims but because its structure quietly offers that key combination of performance and consistency. With a core backbone featuring both the pyridine and phenyl group, capped with a bromine atom, this compound finds its place in labs that focus on the design of new compounds, pharmaceutical intermediates, and materials science.

    What Makes This Molecule Special?

    Every small tweak to the molecular structure can mean big changes in how a compound behaves in the lab. The presence of the bromine at the second position on the pyridine ring opens up versatile cross-coupling reactions, making 2-Bromo-4-Phenylpyridine a frequent choice for onward chemistry. The phenyl group adds both steric and electronic effects, which can determine the selectivity and outcome of a transformation. Researchers familiar with coupling chemistry know how challenging it can be to find heteroaromatic bromides that play nicely under diverse reaction conditions. Over the years, I have seen this molecule help speed up projects where more common pyridines or halopyridines fall short—either due to unwanted side reactions or lackluster conversion.

    Specs That Matter to Working Scientists

    You won’t find much room for compromises in scientific research. Those in the trenches know that batch consistency, melting point, and spectroscopic purity can make or break an experimental plan. Typical samples of 2-Bromo-4-Phenylpyridine ship as a pale solid, with a molecular weight that makes it easy to handle by hand (no clumping or static cling in the jar, sparing you those small logistical headaches that chew through precious time). I have often relied on NMR and HPLC checks, and this compound consistently delivers clean spectra when sourced from trustworthy suppliers, which saves on re-purification and lets you focus on the science.

    Putting It to Work: Where 2-Bromo-4-Phenylpyridine Fits

    Drug development teams, materials scientists, and academic researchers all find their own reasons for keeping 2-Bromo-4-Phenylpyridine on the shelf. For anyone working in medicinal chemistry, it serves as a springboard for creating complex molecules—novel ligands, scaffolds, and intermediates—by leveraging the reactivity of the bromine. Suzuki and Buchwald–Hartwig couplings become less stressful when you have a starting material that resists decomposition and maintains reactivity across a range of conditions. In my own work, it has helped solve bottlenecks in lead compound diversification, giving access to space that less reactive halopyridines simply can’t reach. Colleagues in advanced materials applications highlight how the phenyl group brings new physical properties and can be tailored further to tune electronic characteristics in organic electronics.

    Differences You Will Notice

    Every chemist keeps a mental list of what has worked and what was just good marketing. 2-Bromo-4-Phenylpyridine consistently comes up as a standout next to similar bromopyridines and other aryl halides. Many alternatives get too reactive in the wrong spots or suffer from limited solubility. This molecule cuts through those problems. Compared to plain bromopyridines, the phenyl substitution steers the reactivity, often improving yields and reducing troublesome side products, especially in palladium-catalyzed processes. Aryl bromides without nitrogen can miss the mark when you’re trying to introduce polar functionality or coordinate metals; the pyridine ring here sets 2-Bromo-4-Phenylpyridine apart by offering meaningful interaction with catalysts, which often makes the difference in complicated synthesis steps.

    Why Purity and Consistency Count

    Nobody wants to repeat expensive chemistry because a batch delivered unanticipated surprises. Lab work already comes with enough uncertainty. Reliable suppliers of 2-Bromo-4-Phenylpyridine have earned trust by shipping lots that square with their stated purity, letting scientists push forward with critical steps that depend on high-quality starting material. Impurities in this compound can trigger noisy signals in downstream reactions, so chromatography and spectroscopic verification matter. In my experience, a product with tightly controlled manufacturing standards cuts down troubleshooting time. You get to focus on actual discovery instead of becoming a detective sorting through side reactions and strange analytical results.

    The Value in Research and Industry

    Research dollars and time always run short. Jumping between different aryl bromides often means retracing steps, running new controls, or rebuilding synthetic sequences. The fact that 2-Bromo-4-Phenylpyridine consistently meets the reactivity profile documented in literature jumps out as a real strength. It rarely throws curveballs during scale-up. Waste and byproducts can complicate purification, so being able to count on straightforward post-reaction workup with this compound can dramatically reduce turnaround times. Synthetic groups in pharma and specialty chemicals often rely on these kinds of track records when picking starting materials designed for multi-step syntheses.

    Lessons From the Lab and Literature

    Countless articles document cross-coupling and derivatization work with 2-Bromo-4-Phenylpyridine. Each one helps showcase the breadth of routes made easier by tuning both electronics and sterics in the parent scaffold. Reading through the latest patents and publications, you start to see patterns: frequent citation, broad substrate compatibility, and steady improvement in yield when this reagent is in play. Innovators building ligand libraries or functional materials note its use as a reliable node for attaching new groups, both in small molecule and polymer contexts.

    Handling and Safety in Real-World Use

    There’s comfort in a reagent that behaves as expected in the bottle and at the bench. 2-Bromo-4-Phenylpyridine generally doesn’t demand extreme storage conditions, making it a staple in many chemical stocks. With molecular stability across typical lab temperatures and reasonable resistance to moisture, it demands the usual sensible handling (gloves, avoidance of direct inhalation), but rarely disrupts workflows with strange reactivity or volatility. Nearly every chemist I’ve worked with learns to appreciate this predictability, especially when balancing safety against speed and productivity.

    Common Challenges and Navigating Pitfalls

    No product escapes challenges. In the wrong hands or under poorly controlled conditions, cross-coupling with aryl halides can result in dehalogenation or low yields. Choosing the right catalysts and bases, monitoring temperature, and staying alert to hints of side reactions set apart smooth processes from the ones that eat up your day. Here, I’ve found that consulting both vendor technical notes and recent case studies pays off. The robust literature around 2-Bromo-4-Phenylpyridine gives a roadmap for best pairing with ligands and metals—removing some of the guesswork that comes with more obscure or temperamental reagents.

    Head-to-Head With Similar Reagents

    It’s easy to mistake similar names or structures as offering the same outcomes. Choices between 2-bromopyridine, 4-bromopyridine, and 2-Bromo-4-Phenylpyridine end up mattering in both retrosynthetic logic and practical outcomes. The combined steric profile and electronics shift with the phenyl group in the fourth position, influencing which bond-forming events dominate in the flask. Results from rounds of parallel experiments reinforce these distinctions. When chemists swap out this molecule for “close-enough” alternatives, subtle drawbacks—sluggish rates, more impurities, stubborn purification challenges—creep up. Project managers and senior scientists often remember how an informed decision on a starting material saves entire milestones on the timeline.

    Applications and Success Stories

    You find 2-Bromo-4-Phenylpyridine wherever efficient, creative chemistry is underway. From new drug candidates to advanced materials like OLED precursors and high-performance polymers, its reputation grows through real-world results. Each successful synthesis begins with access to quality materials; more than once, researchers in both large pharma and small startups point to this reagent as the difference-maker on high-impact projects. In several teams I’ve followed, the downstream value shows up in patent filings, time-to-market improvements, and the absence of last-minute rework in pilot plant settings.

    Supporting Smarter Chemistry

    Progress in science comes on the back of reliability and adaptability. 2-Bromo-4-Phenylpyridine enables both. Synthetic teams can step past routine hurdles, since the chemistry books and journals document a wide range of reaction partners and functionalizations. Having dependable physical and chemical properties in your toolkit lets chemists experiment without feeling boxed in by the limitations of the starting material. I’ve seen groups build whole compound libraries off a single, strong parent structure like this, moving quickly from benchtop sketches to viable candidates without losing weeks to troubleshooting or unplanned reformulation.

    What to Look for in a Supplier

    Backing strong chemistry with reliable procurement means looking past glossy marketing. Savvy chemists dig into vendor data sheets, cross-check batch analyses, and watch for partners that document origin, lot purity, and spectral identity clearly. The most respected vendors link to published literature, offer transparency on certifications, and provide material in packaging that prevents atmospheric degradation or contamination. In my own purchases, I favor those suppliers willing to provide small-scale samples and accessible technical support, which matters when scaling up from milligrams to kilos.

    Building Trust Through Consistency

    Teams that focus on repeatable, scalable outcomes value trust in their reagents as much as in their colleagues. With each new synthesis or project, the reliability of reagents sets the baseline for fast progress and robust results. 2-Bromo-4-Phenylpyridine, when handled by reputable providers, justifies that trust. You know what to expect from your reactions, you can plan next steps with confidence, and you can pull from a growing collection of application notes, published protocols, and real-world reports for troubleshooting or inspiration.

    Potential for Innovation With Each New Application

    Curiosity drives chemistry forward. 2-Bromo-4-Phenylpyridine, with its versatile reactivity and well-behaved handling, continues to open unexplored territory in both basic research and commercial discovery. I have seen teams pivot rapidly, plugging this intermediate into new routes based on emerging data or shifting project priorities. Combining robust performance in classic reactions with adaptability for more novel catalysis, the compound continues to draw interest from leaders driving more sustainable, efficient, and creative solutions in synthesis.

    Supporting Data and Quality Assurance

    Anecdotes only go so far in scientific work. Having solid analytical data, supported by matched literature and supplier certificates, guides responsible use of 2-Bromo-4-Phenylpyridine. Robust HPLC and NMR data help verify purity, while melting point checks screen for batch variation. Teams laser-focused on GMP or regulated environment needs rightly scrutinize every parameter. Whether you’re handling milligram-scale R&D or scaling up to commercial production, the quality control practices surrounding this compound set a standard for what modern chemistry expects from its building blocks.

    Addressing Supply Chain and Accessibility

    Chemical procurement challenges hit every research sector in recent years. Lead times, batch recalls, geopolitics, and trade policy all influence how and when scientists can access specialty reagents. 2-Bromo-4-Phenylpyridine tracks well against these issues, with mainstream supply maintaining reasonably stable access. Labs that diversify suppliers and keep a close watch on documentation reduce risks from unexpected delays or shortages. I’ve learned the importance of establishing relationships with several trusted vendors—a lesson that keeps projects moving and reduces downtime when demand spikes or something unpredictable hits global supply.

    Improving Research Outcomes With the Right Tools

    Great science asks for more than clever ideas. It counts on the right tools—smartly chosen, consistently delivered, and credibly documented. 2-Bromo-4-Phenylpyridine fits right into this expectation. The structure and documented performance help both experienced and emerging researchers hit ambitious targets. Whether you are closing in on a new therapeutic candidate, finishing a semester project, or building out new materials for tech devices, this compound’s track record and broad utility make it a smart inclusion on the bench.

    Future Possibilities and Sustainable Chemistry

    Chemistry doesn’t stand still. Sustainable practices, greener synthesis, and reduced-waste goals are shifting many priorities across science and industry. 2-Bromo-4-Phenylpyridine offers a proven starting point for exploring new reaction methodologies, including milder conditions, recyclable catalysts, and lower energy footprints. Teams investigating continuous flow and automated chemistry workflows continue to integrate this compound into their panels, seeking both compatible performance and consistent batch-to-batch quality. Watching these trends, I believe that reagents like this do more than enable today's science—they help shape the next generation of responsible, innovative practice.

    Advice From Experience

    Drawing from long hours in the lab and close review of published studies, my advice centers on careful planning and engaged troubleshooting. 2-Bromo-4-Phenylpyridine rewards attention to detail: clean glassware, fresh catalysts, and thoughtful reaction condition screens produce the best outcomes. When in doubt, start with small-scale exploration and check spectra early; sharing tips and outcomes among team members often brings hidden insights to the surface. Honest reporting of both successes and head-scratchers in professional networks makes it easier for newcomers to avoid common missteps and push the science further.

    Conclusion: Building on a Foundation of Trust and Evidence

    Every decision in chemistry builds on the evidence that came before. 2-Bromo-4-Phenylpyridine earns its reputation by working in the real world, contributing to successful syntheses, reproducible outcomes, and new discoveries across industries. Its distinct structure, dependable reactivity, and well-characterized behavior explain why it stands out. By choosing well-documented, quality-assured materials, researchers can better manage the uncertainties inherent in scientific discovery, move projects forward efficiently, and explore the edges of what is possible in both fundamental and applied chemistry.