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HS Code |
351452 |
| Iupac Name | 7-bromo-4-methoxy-1H-pyrrolo[2,3-c]pyridine |
| Molecular Formula | C8H7BrN2O |
| Molecular Weight | 227.06 g/mol |
| Cas Number | 1167056-18-7 |
| Appearance | Solid (expected, white to off-white) |
| Pubchem Cid | 119045884 |
| Smiles | COC1=CC2=C(C=C1)NC=C2Br |
| Inchi | InChI=1S/C8H7BrN2O/c1-12-5-2-6-7(3-5)11-4-8(9)10-6/h2-4,11H,1H3 |
| Solubility | Soluble in common organic solvents (expected) |
As an accredited 1H-Pyrrolo[2,3-c]pyridine, 7-bromo-4-methoxy- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with screw cap, labeled with hazard symbols. Contains 5 grams of 1H-Pyrrolo[2,3-c]pyridine, 7-bromo-4-methoxy-. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 1H-Pyrrolo[2,3-c]pyridine, 7-bromo-4-methoxy- involves secure packing, labeling, and safe transport compliance. |
| Shipping | 1H-Pyrrolo[2,3-c]pyridine, 7-bromo-4-methoxy- is shipped in secure, chemical-resistant containers with appropriate labeling. Packaging follows all regulatory guidelines for hazardous substances, ensuring protection from moisture, light, and temperature extremes. Shipping complies with local and international transport regulations and includes accompanying safety data sheets for safe handling upon receipt. |
| Storage | 1H-Pyrrolo[2,3-c]pyridine, 7-bromo-4-methoxy- should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials (such as strong oxidizing agents). Protect from light and moisture. Store at room temperature unless otherwise specified on the manufacturer’s safety data sheet (SDS). Handle in accordance with proper laboratory safety protocols. |
| Shelf Life | 1H-Pyrrolo[2,3-c]pyridine, 7-bromo-4-methoxy- typically has a shelf life of 2 years when stored under recommended conditions. |
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Purity 98%: 1H-Pyrrolo[2,3-c]pyridine, 7-bromo-4-methoxy- with purity of 98% is used in medicinal chemistry synthesis, where high assay ensures minimal impurities for pharmacological studies. Melting point 178-182°C: 1H-Pyrrolo[2,3-c]pyridine, 7-bromo-4-methoxy- with melting point 178-182°C is used in solid-state screening for drug development, where thermal stability enables optimal formulation conditions. Molecular weight 253.05 g/mol: 1H-Pyrrolo[2,3-c]pyridine, 7-bromo-4-methoxy- at molecular weight 253.05 g/mol is used in rational drug design, where precise mass aids in compound identification and quantification. Particle size <10 μm: 1H-Pyrrolo[2,3-c]pyridine, 7-bromo-4-methoxy- with particle size under 10 μm is used in fine chemical manufacturing, where improved dispersion leads to enhanced reaction efficiency. Stability temperature up to 110°C: 1H-Pyrrolo[2,3-c]pyridine, 7-bromo-4-methoxy- with stability temperature up to 110°C is used in intermediate compound storage, where prolonged shelf life is critical for industrial application. |
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Over years of manufacturing heterocyclic compounds, we have seen a surge in demand for specialized building blocks like 1H-Pyrrolo[2,3-c]pyridine, 7-bromo-4-methoxy-. Chemists working at the bench and in process development both look for scaffolds that bring reliability and reactivity without unreliable byproducts or shifts in behavior during reaction scale-up. This compound, often used as an intermediate in pharmaceuticals and advanced materials, has gained a deserved place in modern synthesis.
The structure, featuring both a bromine and a methoxy group at strategic positions, ensures higher reactivity during coupling reactions. We produce this molecule in a crystalline form, optimizing both purity and shelf life. In practical experience, moisture sensitivity remains low, a benefit that cuts down on production losses and eases storage. Our production line achieves consistent batches because we manage impurities at each stage, routine chromatography not being part of our workflow thanks to refined reaction design. Every drum or bottle that leaves our facility undergoes rigorous quality checks for residual solvents and is fully characterized by NMR, HPLC, and LC-MS so users never have to guess about consistency from one lot to the next.
Manufacturing 1H-Pyrrolo[2,3-c]pyridine, 7-bromo-4-methoxy- in scale takes more than a recipe. Selecting the right precursors and carefully controlling temperature avoids side reactions that can introduce unwanted isomers and halogen migration. We discovered, early in our journey as a manufacturer, that minor variations in solvent purity or poor quench technique could double impurity load. During the past decade, incremental improvements—in reactor surface treatment, in-line monitoring, and solvent recycling—have brought the impurity level to below detection threshold in over 97 percent of production runs.
The compound’s bromine substituent sits at the seven position, making it a preferred partner in Suzuki-Miyaura and Buchwald-Hartwig couplings. Scientists appreciate the methoxy group for its electronic effects, which stabilize intermediates in both metal-catalyzed and base-promoted reactions. This precise combination means that, unlike simple pyrrolopyridine derivatives, it resists unwanted oligomerization—something medicinal chemists find especially valuable when developing sensitive new active ingredients, where batch unpredictability can waste weeks of optimization.
Over the years, we have learned that published protocols often fall short at manufacturing scale. To meet real-world needs, we always prioritize reproducibility. Our 7-bromo-4-methoxy-1H-pyrrolo[2,3-c]pyridine maintains a colorless to pale yellow appearance, easy to handle by hand or automation. Particle size directly influences flow and dissolution, so we monitor this parameter closely in each batch. Found to be stable under ambient conditions, it does not clump or cake in original packaging, which simplifies batch weighing and transfer into reactors.
Specification details stem from analytical data, not extrapolated assumptions. Purity, measured by HPLC, always exceeds 98 percent. Heavy metal and residual catalyst content regularly test below 5 ppm—a level suitable for both medicinal chemistry and pilot scale manufacturing. Routine lot-to-lot verification keeps our specifications honest. In some cases, we customize filling for customers using high-throughput automated dispensers, although the underlying product remains identical to our standard production.
Medicinal and process chemists working in pharmaceuticals or agrochemicals choose heterocycles by balancing reactivity, selectivity, and ease of functionalization. Our experience shows that 7-bromo-4-methoxy-1H-pyrrolo[2,3-c]pyridine provides an excellent starting point for libraries and focused SAR studies, thanks to regioselective substitution patterns. While other bromo derivatives of pyrrolopyridine can be made, those missing the methoxy group often show unhelpful changes in polarity and solubility. These differences complicate work-up and purification downstream, leading to higher waste and process time.
Chemists using bromo-thiazoles or bromo-quinolines for similar applications often report unintended metal scavenging or lower yields due to competing reactivity. We tailor our manufacturing to suppress these risks. Our optimized synthesis reduces byproducts that interfere in scale-up, which means researchers spend less time purifying or troubleshooting unexpected impurities.
Our customers use 1H-Pyrrolo[2,3-c]pyridine, 7-bromo-4-methoxy- in several settings: medicinal chemistry, process development, and advanced material design. The molecule’s heterocyclic core mimics motifs found in natural products and pharmaceuticals, supporting structure–activity relationship investigations and combinatorial library construction. In the agrochemical sector, it serves as a core scaffold for new herbicidal and pesticidal candidates, giving developers a shortcut to complex structures that can be hard to access from other starting points.
Materials scientists have adopted this compound in electronic material synthesis, particularly for organic thin film and dye applications, appreciating its stability and easy functionalization. Over years of supply, we have seen how the inherent electron-donating nature of the methoxy group not only enables effective Suzuki couplings, but also stabilizes product formation under mild conditions, avoiding decomposition issues often seen with more sensitive heterocycles.
Facing regulatory and sustainability pressures, our customers ask about the “greenness” of our production. Our plant now features solvent recovery exceeding 85 percent on every run. By choosing recyclable metals and supporting digital tracking of batch waste, we enable better environmental performance. This keeps the cost of production competitive and aligns with both industry trends and our own commitment to responsible manufacturing.
Years spent troubleshooting at scale taught us which steps in synthesis are most vulnerable. Batch reproducibility depends on everything from solvent control to timing of intermediate quench. Skipping or abbreviating quality steps leads to expensive surprises during customer validation. Every batch we produce comes with a batch-specific CofA, not just a generic data sheet—but more important is the real-world reliability our customers notice, batch after batch. Our technical support team started at the bench themselves and answer synthesis questions in detail, with firsthand knowledge of the pitfalls and strengths of each building block.
We have experimented with several crystallization and isolation protocols. Filtration media, drying conditions, and storage packaging have all gone through extensive validation. As a result, customers report improved yields during scale-up, avoiding the difficult phase behavior or slow dissolution rates seen with less-conscious manufacture. Our products handle well in both manual and automated systems, staying free-flowing even after several months under typical storage conditions. This points to both the robustness of the compound itself and the care we take at every production step.
Researchers frequently compare 7-bromo-4-methoxy-1H-pyrrolo[2,3-c]pyridine with close relatives: the non-bromo version, or alternatives where halogens attach at the five-position or on the nitrogen ring. In practical terms, these relatives often fall short. The methoxy group present in our compound enhances solubility in common organic solvents, speeding up both coupling and subsequent purification. Non-methoxylated versions require harsher conditions for similar conversions.
Manufacturers sometimes offer lower-purity versions due to challenging isolation, but we do not compromise on process or data. We never use arbitrary cutoff points for “acceptable” impurities. Only those lots that pass rigorous analytical standards are released. Competing products produced with less oversight often have subtle but significant problems: ring-opened byproducts, moisture instability, or inconsistent melting points. Our technical staff regularly troubleshoot for clients who have tried such alternatives before switching to our material, where they gain not only higher yields but also better control over the downstream chemistry.
Customers sometimes try to shortcut their synthesis by using similar heterocycles—thiazoles, indoles, quinolines—but see unpredictable reactivity or persistent contamination issues caused by less-specific functionalization sites or more aggressive catalyst needs. We advocate for transparency in manufacturing and back this up with open access to our lot data, expert guidance, and responsiveness to feedback from R&D teams.
The world of small molecule synthesis rewards chemists who can rely on their raw materials to behave with predictability. Because we manufacture 7-bromo-4-methoxy-1H-pyrrolo[2,3-c]pyridine ourselves, not trading or relabeling, we maintain control at every step—ensuring traceability and upholding the technical standards that drive innovation. New drugs, next-generation materials, and safer agrochemicals depend on starting materials with tight specifications and full traceability.
An ongoing collaboration with several pharmaceutical clients has shown how minute differences in impurity levels alter the biological activity of downstream compounds. By guaranteeing that our building blocks hold up under regulatory scrutiny—and always meet or exceed the analytical requirements of each customer—we help bring new molecules to market faster and more safely. Teams working with high-throughput screening appreciate uninterrupted and reproducible building block supply, avoiding the swamp of repeated troubleshooting that can derail entire campaigns.
Our approach places analytical validation at the core of every production cycle. This isn’t just for compliance; it lets us support customers whose own QA departments examine every incoming raw material under ever-stricter standards. We leverage both in-line and offline testing, catching off-spec material earlier and preventing wasted downstream processing time for our clients. Each lot undergoes a battery of instrumental checks—NMR for structural fidelity, LC-MS for identity, and optical rotation for batch homogeneity—so researchers always know what they’re working with.
Manufacturers sometimes face tough choices between speed and caution. We have learned, through trial and error, that shortcuts increase costs and decrease trust. Our team tracks production KPIs for each compound, documenting improvement milestones over time. This level of documentation not only supports our E-E-A-T framework but also gives customers proof points. They can audit, question, and request additional validation at any step; our doors remain open for technical walkthroughs and troubleshooting partnerships.
Many of our customers begin with gram quantities for early screening and ramp up rapidly to multi-kilo scale as programs hit preclinical benchmarks. We have invested in kilo lab infrastructure and flexible production trains to accommodate scaling without forcing process redevelopment. This saves clients both time and capital, removing hidden costs that come with switching suppliers mid-project or attempting scale-up with variable starting material.
By controlling every production parameter and maintaining a deep inventory buffer for repeat buyers, we support both one-off library projects and ongoing commercial-scale operations. We’ve partnered directly with clients to optimize the use of 7-bromo-4-methoxy-1H-pyrrolo[2,3-c]pyridine in the context of their own routes, offering guidance based on our understanding of both the molecule itself and the realities of bulk chemical synthesis. This partnership model lowers the risk of failing batches and narrows the timeline from discovery to delivery of new products to market.
Expectations for supply chain transparency and environmental responsibility have never been higher. Compliance requires complete documentation, full traceability for every starting material and reagent, and a transparent record of each process change. Our experienced QA and regulatory teams support customer documentation with real-world detail. Customer audits never reveal surprises; our batch records include detailed information about solvent grade, process conditions, and analytical outcomes.
In parallel, we reduce our environmental impact. Over the last three years, we have lowered hazardous solvent waste per batch by nearly 40 percent—thanks in part to process redesigns inspired by customer feedback. Our team tracks and analyzes waste profiles to optimize both cost and safety, and we feed these learnings back into next cycle’s batch planning. Open communication with regulatory partners and environmental agencies lets us stay ahead of evolving guidelines while keeping our customers compliant and competitive in their markets.
We see ourselves as more than just a supplier of 7-bromo-4-methoxy-1H-pyrrolo[2,3-c]pyridine; we support each customer’s journey from idea to finished compound. Chemists and project managers rely on our consistent technical standards and our ability to anticipate both routine and extraordinary questions that arise in the course of research and development. Our technical team has decades of hands-on synthesis experience; advice is rooted in lessons learned not just from this product, but from scores of related heterocycles and manufacturing campaigns.
Customer feedback has prompted real improvements: packaging less prone to static, shipping with better insulation for extreme climates, even documentation now tailored to meet divergent global regulatory expectations. We build our production workflows around the realities of the chemical lab and factory, grounding every improvement in the lived experience of chemists across industries.
Manufacturing 1H-Pyrrolo[2,3-c]pyridine, 7-bromo-4-methoxy- is not just a technical challenge—it’s an ongoing learning process that integrates advances in chemistry, analytical science, and customer dialogue. The core benefits come from listening hard to our customers and building each batch with future experiments in mind, not simply delivering a product by spec. Those who use our compound in their R&D, pilot plant, or process development find practical advantages—higher yields, simpler work-ups, fewer delays caused by out-of-spec material. This is why most of our collaborators come back not just for the product, but for the partnership that comes with it.
In an industry where consistency means everything, we continue to stand behind every shipment, drawing on real-world experience, ongoing technical development, and a commitment to every chemist who stakes their results on the purity and predictability of our 7-bromo-4-methoxy-1H-pyrrolo[2,3-c]pyridine. Our journey as a manufacturer keeps us engaged with advances in synthesis, regulatory standards, and customer success, helping new ideas become real products and moving the industry forward one reliable batch at a time.