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HS Code |
956175 |
| Product Name | 3-Bromo-2-Methoxy-5-Methylpyridine |
| Cas Number | 1401414-83-6 |
| Molecular Formula | C7H8BrNO |
| Molecular Weight | 202.05 g/mol |
| Appearance | Light yellow to brown liquid |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents (e.g., DMSO, ethanol) |
| Smiles | COC1=NC=C(C)C=C1Br |
| Inchi | InChI=1S/C7H8BrNO/c1-5-3-6(8)7(10-2)9-4-5/h3-4H,1-2H3 |
| Synonyms | 2-Methoxy-5-methyl-3-bromopyridine |
| Storage Conditions | Store at 2-8°C, away from light |
As an accredited 3-Bromo-2-Methoxy-5-Methylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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3-Bromo-2-Methoxy-5-Methylpyridine stands out in the extensive landscape of heterocyclic compounds, drawing interest among professionals in pharmaceutical and fine chemical industries. This pyridine derivative, with its unique arrangement of bromo, methoxy, and methyl groups on the aromatic ring, offers a mix of reactivity and versatility often missing from simpler analogues. I recall times in my own research when introducing subtle changes to a molecule’s structure opened up new synthetic possibilities. Here, the strategic bromination at the third position is a prime example of how a single atom can set the stage for further transformations, especially using palladium-catalyzed couplings like Suzuki or Buchwald-Hartwig reactions.
Laboratory work often revolves around solving stubborn problems—sometimes the biggest advances come from one small chemical tweak. 3-Bromo-2-Methoxy-5-Methylpyridine is a perfect illustration of this. The placement of the methoxy group at position two and a methyl at the fifth position allows distinct polarity and reactivity. This makes it easier to direct subsequent chemical modifications compared to unsubstituted pyridines. Having a compound that handles both nucleophilic and electrophilic substitution, without becoming too reactive in unwanted directions, matters a lot when planning multi-step syntheses. The careful balance in its molecular structure is what many chemists value, especially when the end goal is to prepare complex molecules for stringent applications.
What draws experts to 3-Bromo-2-Methoxy-5-Methylpyridine is its practical set of physical and chemical properties. Its molecular formula, C7H8BrNO, and a molecular weight that lands around 202.05 g/mol define what goes into every reaction flask. The characteristic pale yellow to off-white appearance is almost iconic—anyone who has worked long hours at the bench can identify that look instantly. A melting point in the expected range supports swift purification by crystallization, while solubility in common organic solvents, such as dichloromethane or ethyl acetate, facilitates routine workups.
Where some compounds with similar ring substitutions might degrade or polymerize during storage, this one holds up well. Chemical stability often makes or breaks a project’s timeline; losing an intermediate due to unexpected breakdown can derail weeks of effort. From my experience, having a well-characterized intermediate like this can make a world of difference for controlling quality and reproducibility in a synthetic pathway. Stack that with a solid shelf life and minimal fuss under typical lab conditions, and it’s not hard to see why 3-Bromo-2-Methoxy-5-Methylpyridine finds its way into so many research labs and pilot facilities.
In drug discovery and medicinal chemistry, success often depends on how easily and reliably labs can source intermediates that fit modern pharmacophores. 3-Bromo-2-Methoxy-5-Methylpyridine serves as a reliable backbone for developing kinase inhibitors, antimicrobial agents, and central nervous system (CNS) drugs. My time collaborating with medicinal chemists taught me that the fine-tuning of biological profiles starts years before clinical studies, and the right building blocks are crucial for rapid iteration.
Synthetic strategies often turn to this compound for cross-coupling applications, where the bromine atom acts as a handle for appending various complex groups. Its structure also means you can dial in electron-rich or electron-deficient properties with minimal unwanted byproducts. In scale-up settings—where time and cost matter just as much as technical excellence—using intermediates that reliably deliver the same quality each batch keeps workflows smooth. The predictability of 3-Bromo-2-Methoxy-5-Methylpyridine underpins countless patent applications and peer-reviewed papers. Researchers trust it because it supports high yields and minimizes the need for troubleshooting.
The market is crowded with pyridine derivatives, so standing out isn’t easy. Many analogues offer similar substitution patterns but don’t balance reactivity and selectivity as skillfully. Take, for example, 3-Bromo-5-Methylpyridine—removing that methoxy group may seem like a small change, yet it impacts both solubility and reaction selectivity. The methoxy group in the ortho position relative to nitrogen not only helps tune the electron density of the ring but also influences how the compound participates in both nucleophilic and electrophilic aromatic substitutions.
A close look at research trends shows why chemists keep circling back to precisely this variant. Other halogenated analogs, like the chloro derivative, bring their own strengths in certain syntheses. But bromine here offers superior leaving group ability while avoiding the sometimes problematic over-reactivity of iodo compounds. This means that, for repeated use in combinatorial libraries or rapid access to new scaffolds, 3-Bromo-2-Methoxy-5-Methylpyridine generally needs fewer optimization cycles. That’s a tangible advantage for teams pushing strict project deadlines.
Over the past decade, trends in pharmaceuticals and agrochemicals have driven up demand for selective, high-purity intermediates. Large companies and agile startups alike focus on efficiency and sustainability. Every extra purification step increases both cost and environmental impact. I’ve watched process chemists prioritize intermediates that yield fewer side-products and streamline downstream processing. This isn’t just about scaling up; it’s about adapting to stricter regulations and changing market pressures. For these reasons, intermediates like 3-Bromo-2-Methoxy-5-Methylpyridine—ready for cross-coupling, stable over time, and easy to handle—continue to gain traction.
Academic research groups echo that sentiment. When budgets and timelines tighten, there’s less room for error or for troubleshooting mystery impurities. Labs depend on easily available, consistently pure materials. Having spent years in academic settings, I know the frustration of chasing down a batch-to-batch inconsistency. Using trusted intermediates, researchers can focus on new science rather than revisiting quality control issues best solved at the source. 3-Bromo-2-Methoxy-5-Methylpyridine has a reputation for reliability, providing peace of mind in fast-paced discovery environments.
Handling chemicals remains a serious responsibility, no matter how familiar the compound might feel. 3-Bromo-2-Methoxy-5-Methylpyridine echoes the general rules chemists adopt for similar halogenated aromatics. Standard laboratory safety measures—a good fume hood, nitrile gloves, and eye protection—are non-negotiable. While this compound doesn’t present more dramatic hazards than other brominated intermediates, keeping exposures low during weighing and transfers is part of every careful chemist’s routine. Careful labeling and storage in tightly sealed amber bottles helps protect both the product and the people using it.
Many labs continue to refine workflows, centering employee safety alongside experimental efficiency. Labs that train newcomers in the details of safe handling—ventilation, spill response, and proper waste disposal—avoid more incidents and downtime. Experienced chemists often share best habits, learned from both textbooks and the occasional near-miss. Chemistry sometimes operates on the edge of what’s possible; keeping accident rates low depends as much on team culture as on product choice. When a compound like 3-Bromo-2-Methoxy-5-Methylpyridine fits smoothly into these established routines, it’s another plus for daily bench use.
Quality assurance demands more than just a certificate of analysis. Researchers insist on transparent traceability for each lot, tracking everything from raw material origin to packaging details. A decade ago, I learned how unexpected supply chain hiccups could stall entire projects. Since then, the industry trend leans hard toward fully audited supply partners, and suppliers respond by offering more documentation and impurity profiles to meet published standards. High-resolution NMR, LC-MS, and even routine FTIR checks have become the norm for every delivery, catching unexpected impurities or degradation early.
As regulatory scrutiny rises, every link in the research-to-product chain faces more pressure to show compliance and maintain full traceability. Trace-level impurities—once shrugged off as background noise—now command real attention, especially with new EU REACH and US FDA guidelines. The rise of digital inventories and barcoded sample management makes it much simpler to spot deviations before they cascade into costly errors. Teams working with 3-Bromo-2-Methoxy-5-Methylpyridine can put their trust in suppliers who invest in transparency, and those with direct lab experience know how this impacts both short-term experiments and long-term validation efforts.
Balancing budgets with top-tier raw materials keeps chemists and procurement officers on their toes. Worldwide fluctuations in bromine prices or supply chain disruptions—caused by anything from global events to shifts in regulatory landscapes—test even the most robust sourcing strategies. Most chemists I know compare suppliers not just on price per kilo, but on consistency, documentation, and delivery times. The relative simplicity in handling and stable pricing of 3-Bromo-2-Methoxy-5-Methylpyridine means it usually beats out more specialized, unstable intermediates for regular use.
Savvy sourcing teams will stock up when pricing dips, while research leaders plan projects to take advantage of market cycles. As companies push for greener processes and higher throughput, blending procurement strategies with R&D needs calls for close communication across departments. It’s not only about finding the cheapest source, but about building partnerships with reliable suppliers. In my own experience, disruptions in chemical supply can halt an entire project, so the emphasis often shifts to reliability and documented quality.
Sustainability has moved from a buzzword to a core concern across chemical industries. Modern R&D groups place as much value on a product’s environmental footprint as on its technical merits. For a compound like 3-Bromo-2-Methoxy-5-Methylpyridine, the demand for greener synthesis routes has driven major advances in process chemistry. Semi-batch processes that minimize waste, or catalytic systems that extract more product from each gram of starting material, gain more attention. As someone who cares deeply about future-proofing science, I appreciate suppliers who prioritize greener solvents or recyclable reagents in their synthetic methods.
Academic and private sector labs work together to publish greener alternatives—replacing hazardous reagents, reworking purification steps, or exploring continuous flow reactions to boost atom economy. These changes also tend to cut production costs and improve operator safety. Compound-specific improvements, like using smart brominating agents or milder demethylation techniques, ripple out to benefit both manufacturers and end users. With mounting pressure from both customers and regulators, labs are re-examining every aspect of traditional synthesis.
Researchers feel the squeeze from both market competition and regulatory oversight. Adopting robust documentation systems, regular supplier audits, and rapid impurity analysis forms the backbone of a modern chemical sourcing strategy. Digital inventory management also eliminates some of the paper-chase that slows down discovery work. Streamlined procurement helps ensure repeatability and peace of mind, supporting teams across continents who may share raw materials for collaborative projects.
On the technical front, partnerships between academia and industry fuel the development of higher yielding, less energy-intensive synthesis protocols. Process improvements—like in-line purification, closed-system reactions, or solvent recycling—offer multiple wins: less waste, lower energy input, and reduced operator exposure to hazardous materials. Working closely with trusted chemical suppliers, labs can proactively pilot these new methods. That means researchers receive both top-quality intermediates and peace of mind, knowing they are not adding to the environmental burden or introducing unexpected risks.
Looking ahead, the best results will come from collaboration between manufacturers, suppliers, and end-users. Open dialogue allows the discovery of pain points—be it in supply consistency, cost, or regulatory compliance—and prompts real innovation. Workshops and user groups devoted to intermediates like 3-Bromo-2-Methoxy-5-Methylpyridine often spark ideas that cascade into improved practices for a wide range of compounds.
Embracing feedback from both experienced chemists and newcomers creates a culture where incremental change becomes routine. I’ve sat in on many team meetings where a simple tip or fix—born from hands-on experience—inspired a chain of improvements. Shared resources, whether best practice documents or shared batch data, reduce the learning curve for newer team members and reinforce quality across the board.
3-Bromo-2-Methoxy-5-Methylpyridine proves itself as an enduring and valuable intermediate, shaped not only by its chemical profile but also by what it enables for researchers, process chemists, and industry at large. It stands out because it solves real-world challenges—enabling efficient, reliable access to target molecules without introducing unforeseen obstacles or excessive complexity. As the pressures mount for faster discovery cycles, greener workflows, and flawless compliance, compounds like this one remain essential. Those who work closely with such intermediates see firsthand the link between molecular detail and broad sector innovation.