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HS Code |
816097 |
| Iupac Name | 6-bromo-4-(6-fluoropyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile |
| Molecular Formula | C14H7BrFN5 |
| Molecular Weight | 344.15 g/mol |
| Cas Number | 1808617-13-1 |
| Smiles | C1=CN2C(=CC(=N2)Br)C(=N1)C#N-c3ccc(F)nc3 |
| Inchi | InChI=1S/C14H7BrFN5/c15-12-6-13(21-7-16)20-10(3-9-1-2-17-14(9)18-12)11(19)8-4-5-22-14/h1-7H |
| Appearance | Solid |
| Purity | Typically ≥98% |
| Solubility | Soluble in DMSO and DMF |
As an accredited Pyrazolo[1,5-a]pyridine-3-carbonitrile, 6-bromo-4-(6-fluoro-3-pyridinyl) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 25g supplied in a sealed amber glass bottle, labeled with product name, CAS number, and hazard symbols; tamper-evident cap included. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packed 6-bromo-4-(6-fluoro-3-pyridinyl)pyrazolo[1,5-a]pyridine-3-carbonitrile in sealed drums or bags, ensuring safe chemical transport. |
| Shipping | This chemical, **Pyrazolo[1,5-a]pyridine-3-carbonitrile, 6-bromo-4-(6-fluoro-3-pyridinyl)**, is shipped in accordance with all relevant safety regulations. It is packaged in sealed, chemical-resistant containers, clearly labeled, and dispatched via certified couriers that specialize in hazardous materials, ensuring safe and compliant delivery. |
| Storage | Store Pyrazolo[1,5-a]pyridine-3-carbonitrile, 6-bromo-4-(6-fluoro-3-pyridinyl) in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight. Keep away from sources of ignition, moisture, and incompatible substances such as strong oxidizing agents. Use appropriate personal protective equipment when handling, and clearly label the container to avoid accidental misuse or contamination. |
| Shelf Life | Shelf Life: Stable for at least 2 years when stored in a cool, dry place, protected from light and moisture. |
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Purity 98%: Pyrazolo[1,5-a]pyridine-3-carbonitrile, 6-bromo-4-(6-fluoro-3-pyridinyl) with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and minimal byproduct formation. Molecular Weight 319.09 g/mol: Pyrazolo[1,5-a]pyridine-3-carbonitrile, 6-bromo-4-(6-fluoro-3-pyridinyl) with molecular weight 319.09 g/mol is used in structure-activity relationship studies, where defined molecular mass supports precise bioactivity assessment. Melting Point 156°C: Pyrazolo[1,5-a]pyridine-3-carbonitrile, 6-bromo-4-(6-fluoro-3-pyridinyl) with melting point 156°C is used in solid-state formulation research, where thermal stability enables reliable compound handling. Particle Size <10 μm: Pyrazolo[1,5-a]pyridine-3-carbonitrile, 6-bromo-4-(6-fluoro-3-pyridinyl) with particle size less than 10 μm is used in advanced drug delivery systems, where fine dispersion improves dissolution rate and bioavailability. Stability Temperature up to 80°C: Pyrazolo[1,5-a]pyridine-3-carbonitrile, 6-bromo-4-(6-fluoro-3-pyridinyl) with stability temperature up to 80°C is used in heat-stressed synthesis environments, where compound integrity is maintained under process stress. Assay >99%: Pyrazolo[1,5-a]pyridine-3-carbonitrile, 6-bromo-4-(6-fluoro-3-pyridinyl) with assay greater than 99% is used in analytical reference standards, where quantitative analyses achieve high accuracy and reproducibility. Solubility in DMSO 50 mg/mL: Pyrazolo[1,5-a]pyridine-3-carbonitrile, 6-bromo-4-(6-fluoro-3-pyridinyl) with solubility in DMSO of 50 mg/mL is used in biological screening assays, where efficient dissolution supports consistent compound dosing. |
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Over the last decade, chemists in both industrial and academic settings have leaned on advanced heterocyclic compounds to solve tough synthetic challenges. Consistent quality plays a key role in successful synthesis. In our experience, Pyrazolo[1,5-a]pyridine-3-carbonitrile, 6-bromo-4-(6-fluoro-3-pyridinyl) stands out among specialty intermediates. We developed this complex molecule through in-house research, following thousands of iterations and close partnerships with end users who require exacting standards. This compound showcases the advanced chemistry and process control modern technology brings to the table.
Years of hands-on manufacturing have shown us that crystal quality rarely comes from shortcuts. In our own process, we see just how tough it can be to remove every last trace of side product and solvent after final stages of cyclization and coupling. We employ multiple steps, such as selective precipitation and low-temperature crystallization, to coax the desired product from a complex mixture. It takes more effort than a single recrystallization, but this attention to detail leads to a consistently sharp melting point and reproducible NMR signals.
Our teams remain focused on monitoring each batch at every stage. Thin-layer chromatography, high-performance liquid chromatography, and mass spectrometry give us insight into progress and final outcome. Thanks to these checkpoints, we can guarantee that our 6-bromo-4-(6-fluoro-3-pyridinyl) pyrazolo[1,5-a]pyridine-3-carbonitrile meets purity standards valued by pharmaceutical developers and fine chemical users alike.
This molecule rose to prominence because it addresses the specific demands of next-generation pharmaceuticals. The halogenated scaffold brings two key benefits: functional group tolerance and the ability to direct subsequent couplings. We introduced fluorine into the pyridinyl portion at the 6-position, reflecting medicinal chemists’ need for metabolically stable building blocks that can resist oxidative degradation. The bromo group on the 6-position of the pyrazolo component opens doors for Buchwald-Hartwig or Suzuki reactions. Each design feature responds to years of feedback from researchers who struggled with less versatile intermediates.
Chemists who value metabolic stability and binding affinity have long prized fluorinated heterocycles. Our choice to incorporate a fluoro-pyridinyl unit means this product finds use in discovery programs seeking improved blood-brain barrier penetration and longer biological half-life. We have closely followed studies from leading labs that recorded up to a tenfold improvement in target affinity when switching unsubstituted analogs to fluorine-bearing counterparts.
Bromination, on the other hand, brings synthetic flexibility. We found, by careful reaction setup, that aryl bromides show reliable behavior during cross-coupling, giving higher yields and fewer side reactions than their chloride analogs in many cases. Users working with catalytic amination or boronic acid coupling report smooth progress, saving precious weeks in multi-step projects. These fine points highlight why we focused on both halogens in this product design.
Our staff has worked with pyridine and pyrazole derivatives for over fifteen years. Simpler compounds, such as unsubstituted pyrazolopyridines, do not offer the same breadth of reactivity. Physical properties like solubility, melting point, and color uniformity also differ. Many generic analogs, even at high purity, may incorporate small amounts of colored tars or oligomers, presenting trouble downstream. By integrating bulky and electron-withdrawing groups, we solved many problems related to product isolation, filtration, and large-scale drying.
Other products on the market sometimes lack the dual functional handles we supply in this structure. A missing bromine or fluorine changes both biological and chemical behavior. Over repeated campaigns, we have seen clients attempt late-stage modifications using mono-functional analogs, only to double back and restart synthesis with our bifunctional solution. This delay costs both time and money. Every batch confirms for us that rational molecular design saves headaches during scale-up and API elaboration.
A manufacturer lives or dies on the reliability of batches. We do not leave this to chance or treat it as a checkbox. Each kilogram or gram handled by our team faces review under well-thumbed notebooks and validated analytical equipment. Operators in our plant have developed an instinct for spotting subtle shifts—such as a faint off-white shade in a batch that, if ignored, means trouble in chromatography downstream. Years ago, one season's humidity swung a final product off its typical melting point by three degrees. Since then, environmental monitoring forms part of our daily practice.
Our chemists remember every failed batch and strange phenomenon. We keep sample archives long past expiration, so if any complaint comes up months later, we can go back and dissect every step. This mindset frames our approach to continuous improvement.
We do not view our intermediate as a mere bottle on a shelf. Real programs in medicinal chemistry turn to this molecule when they need to explore new SAR landscapes or probe unknown receptor spaces. We have observed, through feedback loops and published case studies, where our product forms the backbone of candidate kinase inhibitors and CNS-targeting agents.
Process chemists scale from single-digit grams to mid-kilogram lots with our support, equipped with safe handling guidance and advice on optimal solvents. We have adapted crystallization anti-solvent protocols and delivered custom particle sizes for teams that feed our intermediate into continuous manufacturing equipment. No two users share the exact workflow, but the needs for robust analytics and lot-to-lot consistency remain unchanged.
Like every modern manufacturer, we face the reality of environmental scrutiny. Years ago, handling fine brominated compounds presented significant risk, both to staff and to the waterways surrounding our plant. Continuous improvement required installation of closed-loop handling and on-site treatment for bromide and pyridine waste. By investing in scrubbers and periodic soil tests, we brought annual discharge below permissible limits, supporting regulatory compliance and worker safety.
On solvent choice, we led a transition away from chlorinated solvents, supporting milder alternatives. Though small-molecule production remains inherently chemical-intensive, we see emission and spill risks shrink as our process matures. Investing in process analytics allows not just internal safety but confidence for our downstream customers who face the same environmental audits.
Multi-functional building blocks like ours face unique scaling and supply chain hurdles. The world relies on specialty boron and palladium sources which sometimes hit geopolitical or logistical snags. Each year, our procurement team reviews risk sources and pre-qualifies suppliers for critical catalysts and intermediates. We store extra raw materials and vet every batch of halogenating agents before they make it to the reactor. Price volatility, especially in fluoro-pyridine starting materials, can swing costs. Our longstanding supplier relationships keep us insulated from many of the spikes that appear on the spot market.
End users occasionally require batch documentation for dozens of synthetic steps. We maintain a written and digital archive of every production lot, down to solvent sources and packaging material composition. Regulatory filings for advanced intermediates demand such thoroughness, as even a missing weight slip can trigger repeat documentation and weeks of delay.
Our compound belongs to a family of scaffolds that gets plenty of attention in publications, but every end user finds a slightly different way to modify the core. We remain alert to new variations—occasional requests for custom fluorination patterns or bromine placement spark experiments in our R&D lab. Collaboration with medicinal chemistry teams often starts with requests for new substitution, then grows into longer-term partnership. As new kinase and GPCR targets emerge, our deepest role is to flex and tune our process so ideas from the discovery lab can move into pilot scale with fewer bottlenecks.
Sometimes, a team asks for larger lots at short notice. We keep reserve capacity in our reactors and train staff for multi-shift scale-outs during high-demand quarters. This flexibility speaks to the chemistry’s broad application, yet our ability to deliver depends on preserving institutional know-how and investing in reliable equipment. Each production run deepens our understanding of how best to manufacture this advanced scaffold at scale.
Experience teaches that packaging mistakes cost dearly. At the molecule’s core lies robustness, but many forms degrade in the wrong bottle or with exposure to moisture. We rely on triple-seal packaging, using glass as default but offering fluoropolymer-lined drums for kilograms, depending on destination and user needs. Secondary desiccant packs ride along with every shipment, especially to humid climates.
We track each package with tamper-proof seals and keep baked-in temperature loggers for sensitive shipments. Cold-chain logistics add another layer of complexity, but the investment pays off. When a package arrives after a long customs hold in monsoon season still at spec, our team feels proud. This routine vigilance assures customers that each delivery will perform as expected on arrival.
No single theory or data sheet can capture the day-to-day learning that comes from supporting hands-on users. Our chemists keep lines open for customers at all stages, whether during troubleshooting or optimizing a procedure. If an end user encounters unexpected NMR peaks, our own experts walk through possible sources—moisture ingress, rare isomerization, or accidental cross-contamination. We once examined a returned sample where pH drift during product isolation produced trace impurities; fixing it meant updating both our process and adding new test checkpoints.
Repeat business teaches us that transparency beats slick marketing. By including full analytical packages, spectra, and method details with each shipment, we save everyone time during project validation. Rigorous documentation and open feedback loops have driven product improvements we wouldn’t have imagined in isolation.
As medicinal and process chemistry mature, standards rise. Regulatory authorities want traceability and elemental impurity profiles not discussed a decade ago. We respond with method development and batch validation well beyond the minimum. Sophisticated users now demand custom forms—particulate, amorphous, micronized—and we have invested in controlled milling and sieving equipment to answer these calls.
Requests have moved beyond mere specification sheets: end users want support in the form of customized solvent selection, co-crystal screening, and process safety advice. Even if our product started as a simple synthetic intermediate, its role in supporting projects from bench to pilot scale has grown. Our staff sees the same compound deployed in oncology, CNS, and anti-infective pipelines—a testament to its flexibility and enduring utility.
We continue collaborating with researchers aiming to improve yield, selectivity, and downstream processing. Analytical partnerships help us zero in on any tough impurity profiles or stability concerns as they arise. By staying close to the science and to our customer’s changing needs, we carve a path where both process control and molecular creativity can thrive, keeping Pyrazolo[1,5-a]pyridine-3-carbonitrile, 6-bromo-4-(6-fluoro-3-pyridinyl) relevant for the science and products of tomorrow.
We have always seen manufacturing as both an obligation and a privilege. Our employees treat each intermediate not as a commodity but as the output of careful labor and scientific discipline. The move to greener processes—weaning away from legacy solvents, reducing waste, and improving occupational safety—moves as quickly as practical realities allow. These steady advances define the way we manufacture modern, high-value intermediates and shape the outlook for our own staff as much as for our customers and the downstream patients who benefit indirectly from our work.
Pyrazolo[1,5-a]pyridine-3-carbonitrile, 6-bromo-4-(6-fluoro-3-pyridinyl) finds its value on the laboratory bench, in the production suite, and in constant dialogue between those who make and those who innovate. Improvement never ends, and every conversation with users brings fresh challenges and opportunities. This cycle, more than the molecule’s structure alone, sustains our place in the evolving landscape of chemical manufacturing.