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HS Code |
112078 |
| Chemical Name | 2-Bromo-6-methoxypyridine |
| Molecular Formula | C6H6BrNO |
| Molecular Weight | 188.03 g/mol |
| Cas Number | 70704-39-1 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 80-83°C at 15 mmHg |
| Density | 1.601 g/cm³ at 25°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as DMSO and ethanol |
| Smiles | COC1=CC=NC(Br)=C1 |
| Storage Conditions | Store in a cool, dry place and keep tightly closed |
| Refractive Index | 1.573 (approximate) |
As an accredited 2-Bromo-6-methoxypyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 2-Bromo-6-methoxypyridine (5g) is a sealed amber glass bottle with a printed hazard label and product details. |
| Container Loading (20′ FCL) | 20′ FCL container loads about 13.5 metric tons of 2-Bromo-6-methoxypyridine, typically packed in 25 kg fiber drums. |
| Shipping | 2-Bromo-6-methoxypyridine is shipped in tightly sealed containers, under ambient conditions, and protected from light and moisture. Proper labeling and documentation in compliance with chemical transport regulations are ensured. The package includes hazard indications, and the compound is typically shipped as non-hazardous, unless otherwise classified by applicable local regulations. |
| Storage | 2-Bromo-6-methoxypyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature, ensuring proper labeling and access only to trained personnel. Follow all relevant guidelines for handling hazardous chemicals. |
| Shelf Life | 2-Bromo-6-methoxypyridine should be stored tightly sealed, protected from light and moisture; typically, its shelf life is 2–3 years. |
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Purity 98%: 2-Bromo-6-methoxypyridine with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures efficient target compound yield. Melting Point 37-40°C: 2-Bromo-6-methoxypyridine with melting point 37-40°C is used in solid-phase organic reactions, where controlled melting facilitates uniform reaction kinetics. Molecular Weight 188.02 g/mol: 2-Bromo-6-methoxypyridine of molecular weight 188.02 g/mol is used in structure-based drug design, where precise molecular mass enables accurate dosage formulation. Stability Temperature up to 70°C: 2-Bromo-6-methoxypyridine stable up to 70°C is used in high-temperature coupling reactions, where thermal stability maintains chemical integrity. Particle Size <100 µm: 2-Bromo-6-methoxypyridine with particle size less than 100 µm is used in homogeneous catalysis, where fine particle dispersion enhances reaction surface area. Residual Moisture <0.5%: 2-Bromo-6-methoxypyridine with residual moisture below 0.5% is used in sensitive organometallic synthesis, where low moisture content prevents unwanted hydrolysis. UV Absorbance 0.05 at 254 nm: 2-Bromo-6-methoxypyridine with UV absorbance 0.05 at 254 nm is used in trace impurity analysis, where low background signal improves analytical accuracy. Assay by HPLC ≥98.5%: 2-Bromo-6-methoxypyridine with HPLC assay ≥98.5% is used in custom synthesis projects, where high assay supports reproducible reaction outcomes. |
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Most folks who have ever spent a day in a research lab know the frustration of hunting for the right reagents when a synthesis hits a stubborn roadblock. Experienced chemists learn to keep an eye out for compounds that bring versatility and reliability to their workflow. One such unsung hero is 2-Bromo-6-methoxypyridine, an aromatic heterocycle with the formula C6H6BrNO. This molecule, with its bromo-nitrogen-methoxy structure, bridges the needs of synthetic chemists from pharma to agrochemicals, and makes tricky transformations possible without the constant worry over purity issues or sluggish yields.
2-Bromo-6-methoxypyridine doesn't draw much fanfare at chemical expos, but any chemist with a few syntheses under their belt understands that the real value of a chemical shows up at the bench. A high-purity grade (>98%) cuts down on garbage side products, so projects move along faster. This product often comes as a pale, crystalline solid, storable at room temperature with minimal fuss. Melting points and weight checks give confidence—especially since purity deeply affects downstream reaction success.
Handling methoxy-substituted pyridines brings its own set of quirks. Add a bromine at the 2-position—just ortho to the nitrogen—and you unlock coupling flexibility while maintaining stability. This means fewer headaches over storage, no exotic conditions to keep it shelf-stable, and better handling when setting up for palladium catalysis or other transition metal work. Unlike some halopyridines, this variant tends to avoid excessive volatility, allowing practical weighing and transfer without significant material loss.
In many labs, chemists turn to 2-Bromo-6-methoxypyridine as a precursor for constructing complex molecules. Its bromo group acts as a reliable leaving group for cross-coupling reactions like Suzuki, Stille, or Buchwald–Hartwig amination. That means valuable access to aryl and heteroaryl derivatives with diverse pharmaceutical or agrochemical activities. The methoxy group at the 6-position tunes both electronic and steric effects, often driving selectivity in the right direction.
In my own work in medicinal chemistry, I've relied on this compound to rapidly introduce a basic pyridine motif decorated with functionality at precise spots. The presence of a bromo by the nitrogen makes it a strong candidate for carbon–carbon or carbon–nitrogen bond formation, letting us build libraries of analogs faster. This doesn't just save time; it directly impacts our chances of finding a new lead compound in a patentable area.
Plenty of halopyridines circulate in the market, but not all offer the same utility. Rising above more common analogs like 2-bromopyridine or 2-chloropyridine, 2-Bromo-6-methoxypyridine taps into a sweet spot. The 6-methoxy tweaks electron density across the ring and can tip the selectivity for functionalization in late-stage synthesis—an edge that matters when molecule crafting becomes cutthroat.
Think about 2-bromopyridine: it's versatile, true, but often overreacts under some conditions, leading to uncontrolled substitution. Swap in a methoxy at position 6, and the tuning creates a more controlled, predictable outcome—fewer byproducts, cleaner purifications. Compare to 3-bromo-4-methoxypyridine: the difference in substitution pattern shifts reactivity. With 2-bromo-6-methoxypyridine, steric effects from both nitrogen and methoxy define the way the catalyst approaches the ring, and this steadies reactivity during metal-catalyzed steps.
Every chemist dreads scaling up a reaction that worked during discovery but collapses in pilot runs because of ambiguous interactions. My experience with this compound shows it scales with surprising grace. Purity holds, and the same reactivity patterns persist from milligram to gram scale—a small comfort in an unpredictable field.
No chemical is perfect. 2-Bromo-6-methoxypyridine sometimes presents supply worries, especially as demand spikes within the pharmaceutical sector. Labs trying to move projects forward can stall out waiting on shipments, and the temptation to settle for lower grades rises when deadlines loom. This kind of pressure breeds risk—side reactions go up, and troubleshooting explosions cut into productivity.
One proven solution is pairing with trusted suppliers that prioritize transparent quality control. I’ve found vendors willing to share batch certificates and reveal their purification process keep things moving. For someone on the receiving end, a simple TLC confirmation and an NMR run can catch most issues. I learned to keep a backup reserve on hand, even if it means budgeting for a bit of overage; standing idle because a key reagent is backordered simply isn’t worth it.
Another point of frustration comes with residue handling and purification. Some pyridine analogs leave behind stubborn aroma or trace contaminants in reaction vessels, requiring aggressive cleaning. 2-Bromo-6-methoxypyridine generally washes out with standard solvents—ethyl acetate or dichloromethane work fine—so glassware returns to service quickly. Less time spent scrubbing and soaking means more actual chemistry gets done.
Drug discovery today truly runs on modularity. Scientists want to bolt together molecules with the same efficiency seen in assembly lines. 2-Bromo-6-methoxypyridine fits cleanly into this model, serving as a connecting piece that shortens routes to new scaffolds. For example, in kinase inhibitor work, the methoxypyridine substructure crops up over and again among hit compounds, where tweaking electronics with methoxy offers a way to dial in potency and selectivity.
In many ways, I see this compound as more than just a “reagent on a shelf.” For biotechs cranking out small-molecule libraries, being able to directly cross-couple at the 2-position of a pyridine with the enhanced influence of the 6-methoxy group allows for diversity with little wasted effort. It’s not just about getting hits; it’s about making the whole process more flexible—right from scaffold construction through late-stage diversification.
The agricultural sector, too, leans on this chemistry. I’ve seen pesticide chemists use 2-Bromo-6-methoxypyridine as a key intermediate, especially in creating molecules resistant to breakdown in the environment. Methoxy’s influence on metabolic pathways gives an edge, resulting in longer field life and a smaller environmental footprint.
For those trained in academia, picking between subtle variations in molecules can feel academic. But in industry, small differences translate to major business outcomes. Compared to 2-chloro-6-methoxypyridine, the bromo variant usually reacts more smoothly in coupling. The carbon–bromine bond—longer and weaker than the carbon–chlorine bond—translates to easier activation under palladium catalysis. That’s not theory; it’s a matter of hours gained or lost on the bench.
Another real difference is in pricing and sourcing. Brominated intermediates cost more than chlorinated analogs, owing to starting material and production complexity. Yet the boost in reactivity and cleaner transformations often make up the difference by saving time, labor, and purification costs.
Each time I’ve had a hard choice between a cheaper chloro-derivative or a more expensive bromo-pyridine, experience nudges me toward bromo, especially when yields and purity are on the line. There’s less batch-to-batch mystery, which gives everyone down the line—analytical chemists, process developers, formulation teams—an easier time.
Compared to other methoxypyridines lacking the 2-bromo, the electrophilic handle of the bromo group radically expands the scope of transformations. In medicinal chemistry, this is the difference between a dead-end scaffold and one that can accommodate dozens of side chains in a matter of days.
Smart purchasing managers and lab heads know that today’s project timelines spin on the reliability of chemical supply. While the market always seem flush with new suppliers, it takes work to sort out those who deliver consistently high-quality material from those who cut corners. With compounds like 2-Bromo-6-methoxypyridine, working with reputable suppliers ensures cleaner NMR patterns, fewer reminders about backordered lots, and much less time lost to rework.
Consistent supplier relationships mean fewer surprises. In situations where a batch question arises, I expect and demand clear communication and documentation. This helps the entire R&D team make decisions based on real data, not marketing fluff. Over the years, sticking with suppliers who invest in analytical transparency has paid for itself in reduced reruns and more reliable project timelines.
Like many heterocyclic chemicals, 2-Bromo-6-methoxypyridine brings responsibility along with promise. Handling with gloves and in a fume hood stands as standard practice, and experienced chemists recognize the specific hazards linked to halogenated pyridines. Disposal requires working alongside environmental health folks to stay within regulatory boundaries.
Waste minimization isn’t just a buzzword—it’s practical lab management. I’ve learned the value of planning reactions to maximize atom economy, running small-scale trials to perfect conditions before embarking on larger runs. Less trash in the drum means fewer headaches during routine inspections, and tighter practices echo throughout the production process.
Across my experience, clear labeling and double-checking compatibility with other bench reagents helps to prevent unexpected incidents. Particularly with brominated aromatics, safeguarding your own health and that of your colleagues never goes out of style.
Chemists at every level crave tools that solve problems without introducing new hurdles. 2-Bromo-6-methoxypyridine gives innovation-minded teams a genuine edge, acting as a launching pad for novel compounds and IP opportunities. Whether the target is a new therapeutic or a crop protection agent, the ability to push boundaries—forging new bonds, exploring new motifs—comes back to the reliability and flexibility built into this molecule.
I’ve seen early-career researchers tap into this compound and later pivot to new projects with confidence because their early success built trust in the chemistry. The payoff surfaces down the line: faster hit-to-lead progression, smoother scale-ups, and fewer late-stage surprises.
Beyond technical features, this compound represents the backbone of workflow. From weekly group meetings to late-night reaction monitoring, its track record for predictability reduces cognitive clutter, making it easier to focus on the bigger picture.
Anyone new to 2-Bromo-6-methoxypyridine learns fast that efficient handling starts with proper preparation. By using glass containers and weighing trays cleaned from previous uses, chemists protect the product from contamination. In my experience, minimal exposure to air and moisture preserves the purity—an airtight container, stored with a desiccant, offers all the protection one needs for most benchwork needs.
Once weighed, the compound moves easily into typical organic solvents required for cross-coupling reactions. Thin-layer chromatography checks track reaction progress efficiently. A reliable bromo-pyridine like this doesn’t gum up TLC plates and seldom stains glassware irreparably.
For those scaling up, my approach remains simple: small pilot runs, careful observation of crystal formation, and patience during extraction. This compound’s predictability translates directly into less solvent wasted, fewer runs to dryness, and less guesswork when moving from milligrams to grams or more.
The solid nature and scant volatility significantly lower risks of accidental exposure or major spillage. Still, using designated transfer funnels and weighing boats curbs unnecessary waste. Routine habit of double-checking batch labels sidesteps those “wrong compound in the setup” moments, which every chemist secretly dreads.
Seasoned professionals who spend years in the trenches of synthetic organic chemistry develop a sense for what compounds deserve respect. 2-Bromo-6-methoxypyridine has earned a permanent spot in my own toolkit—not just because of its synthetic utility, but because it lets chemists reach ambitious targets without detours caused by quirky behavior.
Graduate students benefit from predictable yields and straightforward purifications, which means more robust data sets and fewer stressful troubleshooting sessions. In busy industrial labs, reliability translates directly into productivity. Fewer repeated experiments mean fewer overtime hours logged, which boosts morale and keeps budgets in check.
While each project brings its own hurdles, the right building blocks can make all the difference. Molecules like 2-Bromo-6-methoxypyridine prove over and again that simplicity and reliability in supply chain and reactivity do more than just keep projects alive—they keep the wheels of science turning at a pace that matters.
Researchers today face unrelenting pressure to innovate, publish, and translate findings into real-world impact. In my own journey, every shortcut in dependable reagents meant another shot at a breakthrough—sometimes even months shaved off a development timeline. As a practical problem-solver, I look for tools offering both scope and control, and this compound stands out. Fast coupling, selective substitution, and broad applicability set a foundation for progress.
The march toward new therapies, environmental solutions, and advanced materials needs chemists equipped with dependable components. 2-Bromo-6-methoxypyridine doesn’t just tick boxes in a catalog; it opens creative pathways, fosters teamwork between chemists and process engineers, and keeps projects out of the slow lane. It’s these qualities—plain reliability, broad reactivity, straightforward logistics—that carve out its place in modern science.
As the field pushes forward, the chemists who understand the nuances between similar compounds, who know which bromo-pyridine fits their process, and who can count on quality batch after batch—those are the ones who transform good ideas into winning outcomes. That’s where 2-Bromo-6-methoxypyridine truly delivers.