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HS Code |
226826 |
| Chemical Name | 4-bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine |
| Molecular Formula | C8H6BrN2O |
| Molecular Weight | 225.05 g/mol |
| Cas Number | 950912-95-3 |
| Appearance | Off-white to yellow solid |
| Purity | Typically ≥98% |
| Melting Point | 146-150 °C |
| Smiles | COc1cc2nccc(Br)n2c1 |
| Inchi | InChI=1S/C8H6BrN2O/c1-12-6-3-7-8(9)10-2-5(7)4-11-6/h2-4H,1H3 |
| Storage Temperature | Store at 2-8°C |
| Synonyms | 4-Bromo-7-methoxy-pyrrolo[2,3-c]pyridine |
| Solubility | Soluble in DMSO, slightly soluble in methanol |
As an accredited 4-bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 5g amber glass vial with a secure cap, labeled with product details, warnings, and batch information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packed drums of 4-bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine, palletized and shrink-wrapped for safe, stable international transport. |
| Shipping | 4-Bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine is shipped in tightly sealed containers, clearly labeled, and protected from light and moisture. Transport complies with all applicable chemical safety regulations. The material is handled by authorized personnel, using appropriate packaging and documentation, and shipped under ambient conditions unless otherwise specified by regulatory or safety requirements. |
| Storage | 4-bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Keep the container tightly closed and clearly labeled. Protect from moisture and direct sunlight. Use appropriate chemical storage cabinets if available, and ensure proper secondary containment to prevent spills. |
| Shelf Life | Shelf life of 4-bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine is typically 2-3 years if stored dry, cool, and protected from light. |
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Purity 98%: 4-bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and minimal byproduct formation. Melting Point 178–182°C: 4-bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine with melting point 178–182°C is used in solid phase peptide synthesis, where its defined thermal stability supports reliable process control. Stability Temperature up to 80°C: 4-bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine with stability temperature up to 80°C is used in organic electronics R&D, where it enables consistent device fabrication conditions. Particle Size <50 microns: 4-bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine with particle size less than 50 microns is used in high-speed automated dispensing systems, where uniform powder flow and dosing accuracy are critical. Water Content <0.5%: 4-bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine with water content below 0.5% is used in moisture-sensitive coupling reactions, where low hygroscopicity enhances overall process efficiency. Molecular Weight 241.08 g/mol: 4-bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine with molecular weight 241.08 g/mol is used in computational modeling of drug candidates, where precise molecular property calculations are required. HPLC Assay ≥99%: 4-bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine with HPLC assay greater than or equal to 99% is used in analytical reference standard preparation, where high assay guarantees reproducibility in quantitation. |
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Our team has watched the world of heterocyclic chemistry evolve with the shifting needs of pharmaceutical research and chemical synthesis. Over the past decade, the focus on nitrogen-rich scaffolds and tailored aromatic compounds has increased, powered by demand from fields like oncology drug development and agrochemical discovery. From our vantage point on the factory floor and in the laboratory, 4-bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine stands out as a workhorse for both medicinal and material science applications. Each lot we produce reflects the feedback and challenges our partners share, and it’s these very conversations that shape our approach to its manufacturing and quality control.
Our 4-bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine, defined by the presence of a bromine atom at the 4-position and a methoxy group at the 7-position of the fused pyrrolopyridine backbone, delivers a potent combination of electronic effects and binding site versatility. Its structure allows for reliable synthetic modifications, appealing directly to researchers who need substrates with a balance of reactivity and stability.
We choose our own routes for the synthesis, and those choices influence key features like melting range, color, and impurity profile. Our typical batch achieves a purity of 98% or higher by HPLC, verified right before release, and we pay close attention to minimizing residual solvents and known byproducts. It’s never just about meeting a certificate of analysis. Every kilogram represents multiple rounds of process refinement, checked and rechecked for reproducibility and consistency.
Our manufacturing partners in drug discovery often mention this compound’s ability to streamline late-stage functionalization. The bromine atom opens up possibilities for Suzuki, Buchwald-Hartwig, or other cross-coupling reactions, putting the molecule just a few steps away from libraries of kinase inhibitors and CNS-active agents. Sometimes, university groups contact us for small samples, eager to investigate scaffold-hopping strategies; other times, established pharmaceutical giants place monthly orders as their teams scale up for animal studies. We hear from both ends of the spectrum and receive questions about which other derivatives might behave similarly in ring-activation chemistry.
Chemical informatics studies routinely single out this structure as a privileged motif—bridging the gap between pyridine’s planarity and pyrrole’s electron-rich character. Some of our largest clients use it as a starting point for combinatorial synthesis, enabling the fast production of derivatives by capitalizing on the robust C–Br bond and stable methoxy protection. The fact that it serves as a launching pad for heteroaryl diversification means this compound is never idle on our shelves for long.
We’ve also noticed growing demand from materials chemists, notably among those developing organic semiconductors or optoelectronic devices. The conjugated structure attracts interest for its charge transfer abilities, and the methoxy group provides solubility advantages in common organic solvents—a small tweak in the molecular design that translates to smoother coating processes and fewer aggregation issues.
For those comparing this molecule with other pyrrolopyridines, the impact of substituent choice cannot be overstated. The combination of bromine at the 4-position and methoxy at the 7-position isn’t arbitrary: every variation—such as a fluoro-, methyl-, or chloro-group—leads to distinctive changes in electronic distribution, reactivity, and solubility.
Clients sometimes ask why our facility invests in separate production lines for methoxy- and chloro-substituted versions. Through actual benchwork and subsequent pilot runs, we’ve seen how the methoxy group can modulate electron density across the ring, enhancing certain cross-coupling yields while curbing unwanted side-reactions. A bromo-only derivative may perform well in direct halogenation chemistry but offers less fine-tuning for downstream modifications.
Our 4-bromo-7-methoxy derivative achieves a balance between chemical robustness and synthetic flexibility, making it more forgiving during multi-step synthesis, especially under harsh or moisture-sensitive conditions. Feedback from customers indicates fewer side-products during large-scale coupling reactions if the methoxy group is present; it also improves the compound’s manageability during chromatography. In contrast, closely related analogues without the methoxy group often deliver a stickier, less crystalline material that complicates both purification and storage.
Some users zero in on the melting point difference or altered solubility behavior among derivatives. After shipping thousands of grams across different climates and applications, we’ve gathered enough comments to appreciate how these little tweaks matter—not only for theoretical reactivity but for simple, everyday realities like material handling, solvent choice, and container compatibility over long transit times.
The story of how we manufacture this compound involves constant adaptation. Every step, from bromination to methoxylation, introduces questions about selectivity, scale-up, and reproducibility. Reagents change with global supply chain shocks; what worked at bench scale frequently throws up surprises in a reactor ten times larger. We’ve dedicated process chemists who keep detailed logs, adapting protocols to suit the quirks of every new batch of starting materials.
By sticking close to real-world needs, our production line invests heavily in in-process analytical controls. TLC isn’t enough when customers demand consistent purity batch-to-batch, so we’ve equipped our QC lab with NMR, LC-MS, and crystallography support. Most days, our staff spends as much time verifying and validating results as actually running the chemistry, because even a small shift can influence downstream performance for a demanding client.
Waste management and safety considerations shape how we set up the facility. The presence of brominated intermediates calls for extra care in waste neutralization and solvent recycling—a topic that comes up often with environmental compliance teams. We see it as our responsibility not only to meet regulatory rules, but to contribute to a greener, safer chemical manufacturing ecosystem.
The most frequent comments we field from direct clients highlight speed and reliability. For groups facing tight project deadlines, receiving material that matches previous lots—chemically, visually, and by analytical signature—matters more than any flashy certificate. As the actual manufacturer, our connection to every reaction, every filtration, every drydown step, gives us an edge in troubleshooting issues quickly.
Customers whose supply chains rely on third-party traders or distant distributors sometimes report long lead times and uncertain shelf life. Because our batches come straight from synthesis to packaging—maintaining controlled conditions tuned by years of hands-on experience—clients get not simply a chemical, but a compound shaped by a practical understanding of the realities of research and development.
More than a few clients ask about documentation and traceability. Our in-house record keeping includes both digital and physical logs, linking every batch to a verifiable production history. It’s not just a value-add; it’s the result of lessons learned from decades of quality audits and on-the-ground troubleshooting.
Questions about structural compatibility often arise—can this molecule replace a similar pyrrolopyridine in an ongoing series? Based on customer trials and our own synthetic exploration, we have observed that while substitution patterns change biological activity, the presence of both bromine and methoxy often improves lead-likeness for many drug templates. In empirical kinase inhibitor screens, molecules evolved from our 4-bromo-7-methoxy analog often report improved lipophilicity and binding orientation compared to strictly halogenated analogues.
Every scale-up order brings a new set of process or formulation questions. Will the same reaction conditions work on a five-hundred gram scale? What happens to the solid-state properties after storage at ambient temperature for several months? Fielding these queries shapes our own lab experiments, driving us toward continuous, real-world validation rather than reliance on abstract data alone. If a user observes clumping or poor dissolution, we welcome such reports, often running parallel tests to confirm findings and adapt packaging or drying methods in response.
Looking beyond daily operations, we watch closely as the broader industry explores machine learning-driven drug design and sustainable chemistry. The rise of AI-assisted synthesis platforms shines a new light on functionalized pyrrolopyridines like ours, since their versatility and reaction-friendliness fit well with algorithmically-optimized libraries.
We frequently support academic partnerships to explore greener production methods—such as phase-transfer catalysis and flow chemistry for halogenation steps—hoping to both reduce resource consumption and expand scalability. Every new synthetic protocol that cuts down on steps or hazardous waste not only strengthens our product but keeps us at the forefront of responsible production.
Safety and compliance never leave our workbench. As regulatory frameworks tighten worldwide, we monitor evolving guidelines and vet our products for restricted substance lists, working to deliver documentation that satisfies increasingly complex due diligence checks. We also contribute to industry roundtables on best practices, sharing what we’ve learned through years of small-batch and bulk synthesis. This knowledge-sharing eventually circles back to improve each drum and vial we ship out.
Our view, shaped by years of hands-on synthesis and feedback from both struggling start-ups and global industry leaders, is that the real value in compounds like 4-bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine lies in the convergence of reliability and adaptability. Synthetic success in the modern lab comes down to building on stable, reproducible substrates—something that cannot be achieved without direct chemist involvement at every stage of production.
User stories, from stalled library screens to record-setting yields, inform both our product design and our troubleshooting priorities. The fact that a single functional group adjustment can mean the difference between success and tedious re-optimization keeps us constantly experimenting. Years spent talking to process chemists and people at the bench have taught us which pain points delay delivery or cause costly rework. By maintaining a dialogue with actual end-users, not just procurement managers, we close feedback loops that often get lost in more transactional supply chains.
We have seen genuine challenges among researchers using market-grade material from indirect sources. Inconsistent quality, varying impurity levels, and uncertain shelf-life all contribute to disrupted workflows and lost time. Our batches, by contrast, reflect the accumulated experience our team brings to every synthesis—careful selection of starting materials, consistent process conditions, and final QC rooted in over a decade of iteration. These features reduce re-testing and provide more predictable results in both high-throughput screening and scale-up projects.
Researchers in fields ranging from medicinal chemistry to materials science explain that seemingly minor variations in source material can alter project timelines by weeks. The level of support and technical data readily available from a direct manufacturer translates to fewer false starts and more robust process development.
We rarely see a “set and forget” approach succeed in specialty chemical synthesis. With every new customer inquiry or setback, our manufacturing approach adapts—sometimes by updating purification steps, sometimes by modifying packaging, always with an eye towards practical realities. Learning from failed crystallizations or unexpected bottlenecks, we integrate real user feedback into every production cycle.
Offline, our staff maintains relationships with several academic labs, who often act as unofficial “beta testers” of minor process amendments. Their direct trial results—whether a 2% jump in yield or a faster purification time—feed directly back into our main production line. Small gains in process efficiency or solubility profile build up over the years into compounds that serve users better with every cycle.
Books and journals can only capture so much about the subtleties of chemical manufacturing. Absorbing the nuances that separate a good batch from an excellent one requires years of accumulated knowledge on the floor—how different grades of solvent behave, or which filtration setups deal best with a stubborn precipitate. Our staff keeps process logs stretching back years, including real-world details such as drying times in the rainy season, filtration breakthroughs, and lessons learned from truck shipments in extreme cold.
Direct manufacturing means we get to observe the entire lifecycle of our product, from initial gram-scale tests to ton-scale production and global shipping. The in-depth knowledge our staff carries about each step—what works, what fails, and why—feeds into every lot we ship. For clients, this holistic oversight minimizes uncertainty and keeps projects moving.
Every new request for 4-bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine puts us at the intersection of tradition and innovation. We see that reliability grows out of experience, but improvement always requires curiosity and responsiveness to evolving demand. Drawing insight from years of direct engagement, process optimization, and hands-on troubleshooting, our facility stands committed to delivering specialty building blocks that empower scientific progress.
In the world of fine chemicals, the most sought-after products are those that balance processability, reactivity, and quality. As direct manufacturers, the pride we take in each lot of 4-bromo-7-methoxy-1H-pyrrolo[2,3-c]pyridine reflects not only technical know-how, but a tangible investment in our customers’ long-term success. We move forward guided by lessons learned at the bench, on the production line, and in ongoing dialogue with the worldwide community of chemical innovators.