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HS Code |
903218 |
| Product Name | 2-Bromo-4-Methoxybenzonitrile |
| Cas Number | 63065-16-7 |
| Molecular Formula | C8H6BrNO |
| Molecular Weight | 212.05 |
| Appearance | Off-white to light beige solid |
| Melting Point | 58-62°C |
| Solubility | Soluble in organic solvents such as DMSO, DMF |
| Smiles | COC1=CC(=C(C=C1)C#N)Br |
| Inchi | InChI=1S/C8H6BrNO/c1-11-8-3-2-6(5-10)7(9)4-8/h2-4H,1H3 |
| Purity | Typically ≥98% |
As an accredited 2-Bromo-4-Methoxybenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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Walking through the world of fine chemicals, certain compounds quietly punch above their weight. 2-Bromo-4-Methoxybenzonitrile is one of those, sitting at a crossroads of utility and specificity. At first glance, it might seem like just another white crystalline powder, but I’ve seen how this molecule can make or break a synthetic route, especially for research teams and pharma labs aiming to get ahead of the curve. For those building custom molecular frameworks or forging specific bonds, the structure—with its bromo substituent and methoxy-nitrile pairing on a benzene ring—serves as both a foundation and a tool.
Let’s strip away the fluff. This compound carries the formula C8H6BrNO and sits comfortably at a molar mass of about 212.05 g/mol. What makes it stand out is the exact positioning of its bromine and methoxy groups. Instead of grabbing a more common bromo-benzonitrile, chemists seek this variant because of how that methoxy group at the para position changes the electronics of the whole molecule. Reactions that look straightforward on paper often turn sideways if precursors aren’t precisely matched, so getting this substitution pattern right pays off in both yield and control downstream.
Researchers zero in on 2-Bromo-4-Methoxybenzonitrile for one main reason: reliability. For years, I’ve watched colleagues rely on it to whip up substituted phenols, new aryl ethers, or to spin off aryl nitriles. The bromo group opens doors for cross-coupling reactions, particularly Suzuki and Buchwald-Hartwig protocols. Chemists serious about library diversity start with this compound. The methoxy function tweaks reactivity, often dialing in perfect reaction rates or boosting selectivity when that last ten percent of purity or yield just won’t come easy with other intermediates.
I have seen this compound’s blueprint showing up in advanced research, from kinase inhibitor scaffolds to fragrant molecules in specialty fragrance development. Its flexibility comes not just from its own chemistry but from how it links to other building blocks, allowing designers to swap out substituents and shift the focus of activity with minor modifications.
The market runs deep with benzonitrile derivatives. Still, you won’t find many with this exact balance of reactivity and stability. For folks deep in chemical R&D, it’s tempting to cut corners with a less costly bromo-benzonitrile or to reach for something unsubstituted. The trouble hits when pursuing clean cross-coupling or a specific electron profile. Unsubstituted analogs don’t offer the same reactivity profile, especially under the demands of high-throughput research. In practice, skipping the methoxy usually means extra side products, more purification, and slower timelines.
The methoxy group isn’t just a passenger. In more than one synthesis, it acts as a pacemaker for the entire reaction, steering selectivity and limiting over-reactivity. Ask any bench chemist who’s watched a reaction crawl or overshoot; that little group can mean the difference between crude chaos and elegant simplicity.
Out on the manufacturing floor, consistency takes priority. 2-Bromo-4-Methoxybenzonitrile shows up with a solid track record for lot-to-lot reliability—purity generally comes in above 97%, with controlled melting points that make milling and handling routine. Comparing scale-up runs of similar intermediates, I have noticed this compound causes fewer headaches related to batch purity and process reproducibility.
Formulation teams don’t just want reactivity—they want consistency. That’s become more valuable as companies chase speed and cost-efficiency. Not every benzonitrile or bromo compound can be ground, dissolved, and filtered with this level of predictability. I’ve watched countless times as scale-up projects benefit from easy handling, thanks to crystal habit and flowability that doesn’t complicate automation or weighing.
With chemical regulation tightening (especially in the EU and North America), 2-Bromo-4-Methoxybenzonitrile manages to avoid the biggest regulatory roadblocks seen with polybrominated or heavily halogenated compounds. While every lab tracks waste and disposal, this compound’s single bromo atom keeps things manageable. Handling and environmental protocols generally follow routine organobromide practices—gloves, goggles, and sensible ventilation. Its standard property set keeps it practical to manage mid-scale safety and storage, compared to more reactive or volatile halides.
Concerns around workplace safety often revolve around vapor exposure or dust inhalation, and here, this solid’s low volatility helps. In my experience, the touchpoints for exposure are familiar: transfer and weighing. With good lab practice in place, spill and exposure risks land at the lower end for specialty chemicals of this class.
Every chemist has war stories about tricky intermediates. I remember one lab stretch where we tried to shortcut a target molecule using cheaper, “similar” starting points. More time went fighting stuck reactions and low yields than making progress. Switching to 2-Bromo-4-Methoxybenzonitrile, with its tuned electronics, sliced the work in half. The reaction tracked better, fewer dropped steps, and cleanup turned from a dreaded scrub into a manageable step. Stories like this repeat around the world, especially for startups and niche pharma labs who can’t afford to bankroll lengthy purifications.
Academic teams, especially those spinning up new combinatorial approaches, lean on this compound because it speeds up the troubleshooting. Just last spring, I watched a graduate student pivot from a dead-end path riddled with tars, simply by locking in this intermediate. After that, the whole group shifted to a workflow that finished weeks ahead of original projections.
Pharmaceutical research gets the most press, but this compound finds its way across chemical sectors. Specialty pigments, agrochemical discovery, and advanced materials research all draw from the same batch of 2-Bromo-4-Methoxybenzonitrile. Fragrance teams look to build stable aromatic backbones, sometimes reaching for it when other routes prove slow or unpredictable.
Polymer scientists—always keen on aromatic nitriles—often drop it into novel resin synthesis because it allows for selective modifications and consistent performance. The presence of the bromo group opens cross-linking opportunities, and the methoxy substitution ensures manageable reactivity during extrusion or curing. Working with a library of structurally similar compounds makes it easier to see why this one wins out so often when bench time is money and shelf stability counts.
Even with its advantages, researchers wrestle with real questions about quality, sustainability, and value. Is the price justified? Can procurement get repeatable purity, or does lot-to-lot variability sink the ship? In my experience, sticking with manufacturers who batch test and certify past the minimums solves most problems—requesting documentation for purity, moisture, and even crystallinity helps labs maintain good results.
I have seen teams falter when they chase rock-bottom pricing without verifying specs; more than once, cost savings on intermediates got wiped out by added time for purification or wasted whole-batch syntheses. Building strong supplier relationships, even if it costs a few percent more, ensures process stability that pays back in real results.
Certain research projects benefit from putting every incoming lot through a quick NMR and melting point check. Not everyone has access to those tools, but larger teams definitely keep a lab notebook full of quality data. This simple step catches off-spec material before it gums up the workflow.
Sustainability pressure isn’t letting up, and the chemical community faces tough questions about raw materials, by-products, and manufacturing emissions. 2-Bromo-4-Methoxybenzonitrile stands up well in this conversation, thanks to its single step bromo-introduction and the stability of its methoxy group. Labs committed to green chemistry often use this intermediate not because it sounds flashy, but because it dodges the complexity of heavily fluorinated or multiply halogenated alternatives.
Shorter synthesis routes, higher yields, and fewer purification stages bring down the resource footprint. Even a small percentage boost in yield translates into thousands of liters of solvent saved at the commercial scale. I’ve sat in on green chemistry audits where this molecule gets called out as a smart choice by sustainability consultants, compared to legacy routes that burn through more hazardous reagents.
Early-stage adoption sometimes stalls when teams try to cut corners or retrofit old experimental runs. Retooling older syntheses to leverage this intermediate takes planning; skipping that step usually lands labs back at the starting block. Taking time to map out reaction conditions—solvent, temperature, catalyst—saves effort in the long run.
Working with students and interns has taught me that education makes all the difference. Once they’ve compared similar routes side by side, weighing not just yield but time and cleanup, the tradeoffs become clear. This learning curve pays back quickly, but it’s one hurdle that can keep teams from using this product to its best advantage.
Across industry and academia, teams stake big deadlines on “little” choices like picking out the right starting material. Over the years, it’s become obvious that 2-Bromo-4-Methoxybenzonitrile’s subtle chemistry keeps it near the top of shopping lists, even as competitors enter the market. Real-world synthesis favors compounds that deliver—on time, on spec, and without blowing up budgets on the cleanup desk.
Tighter regulatory landscapes and greater pressures on supply chain tracking only emphasize why transparent quality and documentation matter. Responsible usage, combined with consistent supply, delivers the reproducibility that research demands now more than ever. The industry keeps shifting, but the fundamentals don’t change.
In a world tilted toward new breakthroughs and faster pipelines, the value of 2-Bromo-4-Methoxybenzonitrile goes beyond its chemical formula. It has grown into an essential tool for those focused on practical outcomes—this compound demonstrates that real progress in chemistry often arrives through reliability, purity, and thoughtful selection just as much as bold new discoveries. For those aiming to deliver results or spark the next innovation, the right starting materials still hold much of the key.