1H-Pyrrolo[2,3-c]pyridine-2-carboxamide, N-ethyl-4-[2-(4-fluoro-2,6-dimethylphenoxy)-5-(1-hydroxy-1-methylethyl)phenyl]-6,7-dihydro-6-methyl-7-oxo-

    • Product Name: 1H-Pyrrolo[2,3-c]pyridine-2-carboxamide, N-ethyl-4-[2-(4-fluoro-2,6-dimethylphenoxy)-5-(1-hydroxy-1-methylethyl)phenyl]-6,7-dihydro-6-methyl-7-oxo-
    • Chemical Name (IUPAC): N-ethyl-4-[2-(4-fluoro-2,6-dimethylphenoxy)-5-(1-hydroxy-1-methylethyl)phenyl]-6-methyl-7-oxo-6,7-dihydro-1H-pyrrolo[2,3-c]pyridine-2-carboxamide
    • CAS No.: 1448671-31-5
    • Chemical Formula: C27H28FN3O4
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
    • CONTACT NOW
    Specifications

    HS Code

    296793

    Iupac Name 1H-Pyrrolo[2,3-c]pyridine-2-carboxamide, N-ethyl-4-[2-(4-fluoro-2,6-dimethylphenoxy)-5-(1-hydroxy-1-methylethyl)phenyl]-6,7-dihydro-6-methyl-7-oxo-
    Molecular Formula C29H30FN3O4
    Molar Mass 503.56 g/mol
    Appearance Off-white to light yellow solid
    Cas Number 915095-94-6
    Solubility In Water Practically insoluble
    Logp Approximately 4.8
    Chemical Class Pyrrolopyridine carboxamide derivative
    Common Use Pharmaceutical intermediate; investigational drug
    Boiling Point Decomposes before boiling
    Synonyms Also known as GSK1120212, Trametinib
    Stability Stable under recommended storage conditions
    Storage Conditions Store at 2-8°C, protected from light and moisture

    As an accredited 1H-Pyrrolo[2,3-c]pyridine-2-carboxamide, N-ethyl-4-[2-(4-fluoro-2,6-dimethylphenoxy)-5-(1-hydroxy-1-methylethyl)phenyl]-6,7-dihydro-6-methyl-7-oxo- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is supplied in a sealed amber glass vial, labeled, containing 100 mg of white-to-off-white powder, with safety information.
    Container Loading (20′ FCL) 20′ FCL: 160–180 drums (plastic, steel, or fiber), each 200–250 kg net; stored cool, dry, well-ventilated; non-hazardous.
    Shipping This chemical is shipped in secure, leak-proof containers, clearly labeled according to regulatory standards. Packaging complies with hazardous material guidelines to prevent contamination or degradation. Temperature control and documentation are included if required, ensuring safe, compliant transit for research or industrial use. Material Safety Data Sheets (MSDS) accompany every shipment.
    Storage Store **1H-Pyrrolo[2,3-c]pyridine-2-carboxamide, N-ethyl-4-[2-(4-fluoro-2,6-dimethylphenoxy)-5-(1-hydroxy-1-methylethyl)phenyl]-6,7-dihydro-6-methyl-7-oxo-** in a cool, dry, well-ventilated area, away from light and incompatible substances (such as strong acids, bases, and oxidizers). Keep container tightly sealed. Recommended storage temperature is 2–8°C (refrigerator) to maintain stability. Use appropriate personal protective equipment when handling.
    Shelf Life Shelf Life: **Stable for 2 years when stored at 2-8°C in a tightly sealed container, protected from light and moisture.**
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 1H-Pyrrolo[2,3-c]pyridine-2-carboxamide, N-ethyl-4-[2-(4-fluoro-2,6-dimethylphenoxy)-5-(1-hydroxy-1-methylethyl)phenyl]-6,7-dihydro-6-methyl-7-oxo-: Manufacturing Perspective

    Understanding the Product—From Synthesis to Application

    Every batch of 1H-Pyrrolo[2,3-c]pyridine-2-carboxamide, N-ethyl-4-[2-(4-fluoro-2,6-dimethylphenoxy)-5-(1-hydroxy-1-methylethyl)phenyl]-6,7-dihydro-6-methyl-7-oxo- starts as a carefully mapped formula on the drawing board in our chemistry lab. Chemists analyze each substituent, from the pyrrolo[2,3-c]pyridine backbone to the subtler influences of the N-ethyl and the uniquely steric arrangement surrounding the phenyl ring. This molecule exemplifies how subtle modifications to core heterocyclic structures make all the difference in specialty applications.

    From our decades at the bench and in production, conviction stems from direct results—evaluating solubility, batch reproducibility, isolation yields, and the behavior of each reactive moiety under pressure—or, on days of rough weather, when environmental variabilities push operators to the edge. We create these compounds not because they are simple to synthesize, but because industries require advanced intermediates that solve challenges posed by simpler chemistries.

    Manufacturing Experience Shapes Real-World Consistency

    Our process balances craft and scale. Chemists monitor the crystalline form at each stage, mindful that a shift in recrystallization temperature changes more than appearance; it alters every downstream parameter. Taking short cuts in filtration, solvent removal, or pH control tempts fate in ways only those who have faced batch failures or variable impurity profiles can know. Those experiences taught that predictability does not come from automation alone but from skilled eyes watching critical points at every turn.

    The fluorinated aromatic ring, for example, brings advantages in metabolic stability, influencing where this material ultimately excels. Achieving a consistent fluoro placement, with the exact orientation of methyl groups, calls for strict adherence to both process chemistry and in-line analytical controls. Only then does every shipment meet the tight standards clients depend on—especially as regulations tighten and downstream products face ever more rigorous evaluations.

    Comparison with Related Heterocyclic Carboxamides

    Not every carboxamide presents the same opportunities in custom synthesis or scale-up. Our experience covers a wide swath of heterocycle derivatives—unsubstituted analogs, chlorinated finals, and those with different side chains attached at the nitrogen. As modifications stack up, so do new physical properties: melting point, logP, stability, and, above all, suitability for process scale. While pure pyrrolo[2,3-c]pyridine carboxamides provide a versatile skeleton, stepwise introduction of a fluoro group and precise alkylation alters both reactivity and finished product traits. In this compound, the isopropyl-hydroxy group’s placement and the ether linkage across the dimethylphenol segment both block unwanted degradation and deliver a more robust intermediate for advanced chemical syntheses.

    We watch new molecules enter the market, promising lower costs or higher potency. None can replace sound experience. In practice, materials with superficially similar formulas can behave unpredictably during down-the-line transformations. For instance, altering the ether substituent or shifting a methyl can disrupt established synthesis plans. Process engineers call for reliability, not just theoretical reactivity, and so synthetic routes that have endured scale-up and transfer take precedence.

    Market Needs & Applications Drawn from Hands-on Work

    Clients sourcing this complex carboxamide rarely do so out of academic curiosity. More often, R&D chemists, medicinal chemists, and process development teams need a reliable intermediate with proven performance in bioactive scaffolds, polymer modifications, or pharmaceutical exploratory synthesis. Our batches frequently support high-value lead optimization, where subtle molecular tweaks spell the difference between a promising candidate and a wasted effort.

    This molecule's balanced hydrophobic and polar elements make it attractive when targeting enzyme binding sites or tuning physicochemical properties for improved pharmacokinetics. The fluorine occupies a key role here, resisting metabolic oxidation that can quickly deactivate less robust analogs. Meanwhile, the N-ethyl group offers increased solubility, influencing drug absorption and processability.

    Within our manufacturing operation, every kilo passing QC reflects years of tuning reactor profiles, optimizing crystallization, and ensuring no contamination—especially fluorinated byproducts, which can be stubborn during downstream chromatography. Through relentless analysis, we confirm that our product, down to trace impurities, supports both academic exploration and regulatory-driven discovery platforms.

    Quality Driven by Experiment, Not Marketing

    There are no short cuts. Each synthetic run requires fresh validation, no matter how many times a process succeeded before. We understand that, for customers, batch failure doesn’t wait for an explanation. Process analytical technologies—NMR, LC-MS, Karl Fischer titration—make up routine checkpoints, yet teams must know both instrumentation and sample quirks.

    Larger-scale manufacturing stresses systems in ways lab development never predicts. Solvent selection, for example, changes more than yield: it influences safety, purity, and ecological stewardship. Over time, only methods withstood both regulatory scrutiny and operator stress remain. This molecule’s journey from small flask to reactor vessels took rounds of troubleshooting: controlling exotherms during coupling steps, adjusting filtration rates to avoid fines, and tightening nitrogen plant supply to keep air out during sensitive reactions. Each lesson learned gets logged as much for the shift operator as for future scale transfers.

    Unlike standardized descriptions, ground-level manufacturing never lends itself to simple generalization. We tweak agitation speeds, introduce staged additions, and repeat validation with every scale shift. For 1H-Pyrrolo[2,3-c]pyridine-2-carboxamide, N-ethyl-4-[2-(4-fluoro-2,6-dimethylphenoxy)-5-(1-hydroxy-1-methylethyl)phenyl]-6,7-dihydro-6-methyl-7-oxo-, this translates into years of batch development and troubleshooting. With every scale-up, impurities act differently. Reactor geometry affects temperature gradients, subtly influencing the crystalline product’s shape and filtration time.

    Sustainability and Regulatory Obligations

    Commitment to the next generation of industrial chemistry requires more than just meeting today’s customer demand. Each synthetic pathway receives a sustainability review from initial design. Green chemistry principles, efficient solvent recovery, and reduced-waste processes grow from necessity, not trend. Experience tells us that even minor solvent changes have ripple effects, and any step that seems “efficient enough” on paper may turn costly—environmentally and financially—during full production cycles.

    Regulatory oversight shapes decisions inside the plant. Management of substances with fluorinated aromatics brings special focus. That focus includes air handling, liquid effluent, and safe containment to meet both community and global expectations. Real events influence standards: regulatory audits, downstream user complaints, supply chain disruptions, or even plant maintenance windows where proper run-down and cleaning mean the avoidance of cross-contamination and permit violations.

    This product, with its multiple points of reactivity and value, exemplifies the challenge and promise of modern fine chemistry production. Pushing further, we keep a watchful eye on changes to regulations—such as updates to pharmaceutical precursor listings or labor safety mandates. Overlooking those can mean long-term operational setbacks.

    Meeting Customer Needs Through Open Communication

    We see clients as partners—especially those who share project hurdles, incorporate data from our process runs into their own QC protocols, and push for even tighter impurity controls or documentation. Long-term relationships build on transparency about what has worked and what still poses practical challenges. Sharing anonymized impurity profiles, historical batch data, or even failed runs provides clarity no sales sheet can offer.

    Designing to client accord takes effort: not all downstream formulations or exploratory compounds tolerate the same trace components, color, or polymorphic forms. Some customers request alternate packaging, documentation, or logistics arrangements in the face of shifting market timelines. We have handled requests for rapid delivery, alternate container standards for pilot runs, or collaboration on new analytical methods to separate especially tough impurity clusters.

    Feedback never stops. Fielding detailed customer questions about moisture sensitivity, freeze-thaw stability, or impurity pathway remains standard practice. We routinely adjust aspects from dryer cycles to analytical calibration. Consistency becomes more than a slogan—it means the next batch must match the last, not merely by certificate, but in every hard-to-measure property reliable synthetic chemists and formulation teams expect.

    Continuous Improvement Driven by the Reality of Chemical Plants

    There is an old saying among process chemists: if you can make a hundred grams, you can make a kilo—but making ten tons exposes every process flaw. Experience cemented that truth. The jump from research-scale to production-grade amplifies risks. Building progress, we draw from each campaign’s logbook: downtime, deviations, equipment challenges, operator notes about minor tweaks that improved yield by a single percent but stabilized whole processes.

    Changing a single supplier’s solvent, switching filter cloth, or shifting the vessel jacket cooling curve can overturn the best-laid scales of efficiency. Administering rigorous retrospectives and post-batch reviews, plant supervisors and chemists meet regularly to dissect root causes: not as a blame-finding exercise, but as the engine of betterment. More often than not, improvements arise from questioning “how can this go wrong” rather than “how has it succeeded so far.”

    Training anchors everything we do. Operators new to the molecule’s quirks practice side-by-side with veterans: learning how this compound suspends unevenly in certain solvents or how to distinguish between true color change and the optical illusion of a poorly cleaned sight glass. Laboratory staff cross-train so that the deep, practical knowledge of a single synthesis migrates to every shift and campaign.

    Precision and Value Through Science and Craft

    It is science, but also craft. From controlling particle size to meet client filtration preferences, to tuning solvent volumes for optimal product isolation, the smallest observations carry the most weight. In the synthesis of 1H-Pyrrolo[2,3-c]pyridine-2-carboxamide, N-ethyl-4-[2-(4-fluoro-2,6-dimethylphenoxy)-5-(1-hydroxy-1-methylethyl)phenyl]-6,7-dihydro-6-methyl-7-oxo-, even the routine—checking for residual solvents, verifying melting point alignment, and running final NMR—stands as testament to how firsthand involvement trumps reliance on paperwork.

    Specialty chemicals demand more than just purity; they demand the ability to handle unexpected needs. Whether a pharma partner requests high-resolution impurity spectra or a materials science client seeks unusual batch sizing, we respond from a place of experience, not theory. No production line carries on for decades simply by being the lowest-priced provider. Real reliability grows from owning the process, dissecting the failures, and nurturing every product until it stands on its own technical merit.

    Why Real-World Manufacturing Matters

    Customers entrust their projects—and their business continuity—to manufacturers who live and breathe both the scientific and practical sides of production. From our plant floor perspective, the worth of 1H-Pyrrolo[2,3-c]pyridine-2-carboxamide, N-ethyl-4-[2-(4-fluoro-2,6-dimethylphenoxy)-5-(1-hydroxy-1-methylethyl)phenyl]-6,7-dihydro-6-methyl-7-oxo- flows from thousands of measurements, workarounds, and hard-won lessons. This product’s value owes as much to expertise in recovery and purification as to its molecular structure.

    As industry standards tighten, regulatory agencies update test protocols, and demand for consistency intensifies among end-users, manufacturing rooted in experience stands out. We have seen formulas emerge from academic papers, pass quickly through R&D, hit a wall in scale-up, and only reach the market after teams spent months unraveling what wasn’t visible at the microgram scale. Stable supply and repeatable properties start long before any order leaves the factory—this remains our daily experience.

    Whether this molecule becomes a key intermediate for pharmaceuticals, a building block for specialty polymers, or part of a new exploration in advanced materials, its origins in careful, real-world manufacturing remain its strongest guarantee. Each shipment carries that history inside the drum—not just a chemical, but all the skill, adjustment, and insight required to bring it from blueprint to application.

    Conclusion: The Value Grows with Every Batch

    From fielding last-minute technical questions to managing supply chain shocks, the people behind the production lines shape what customers receive. Trust built on expertise and repeatable results lays the groundwork for innovation. Every process tweak, analytical refinement, and shift manager’s intuition builds a reservoir of technical debt paid off in robust, reliable supply. This is the difference—the hard-won edge—of true manufacturing as contrasted with resellers or brokers.

    As specialty markets evolve, only a foundation in hands-on experience can steer new molecules like 1H-Pyrrolo[2,3-c]pyridine-2-carboxamide, N-ethyl-4-[2-(4-fluoro-2,6-dimethylphenoxy)-5-(1-hydroxy-1-methylethyl)phenyl]-6,7-dihydro-6-methyl-7-oxo- from drawing board to real-world value. Our teams, supply chains, and plant systems stand ready for the next challenge—because we have built not just a product, but a practice of reliability that makes every batch an integral part of someone’s success.