4-fluorothieno[2,3-c]pyridine-2-carboxylic acid

    • Product Name: 4-fluorothieno[2,3-c]pyridine-2-carboxylic acid
    • Chemical Name (IUPAC): 4-fluoro thieno[2,3-c]pyridine-2-carboxylic acid
    • CAS No.: 929782-45-4
    • Chemical Formula: C8H4FNO2S
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    226942

    Chemical Name 4-fluorothieno[2,3-c]pyridine-2-carboxylic acid
    Molecular Formula C8H4FNO2S
    Cas Number 328565-99-1
    Appearance White to off-white solid
    Purity Typically >98%
    Solubility Soluble in DMSO, slightly soluble in water
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Smiles C1=CN=C2C(=C1F)C=CS2C(=O)O
    Inchi InChI=1S/C8H4FNO2S/c9-5-2-10-7-6(11)1-3-13-8(7)4-5/h1-4H,(H,11,12)
    Synonyms 4-Fluoro-thieno[2,3-c]pyridine-2-carboxylic acid

    As an accredited 4-fluorothieno[2,3-c]pyridine-2-carboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 5g amber glass vial, sealed with a screw cap, labeled with product name, quantity, and safety information.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 4-fluorothieno[2,3-c]pyridine-2-carboxylic acid: Secure, palletized drums, compliant labeling, moisture-protected, optimal stacking, full capacity utilization, safe chemical transportation adhering to international regulations.
    Shipping 4-Fluorothieno[2,3-c]pyridine-2-carboxylic acid is shipped in a tightly sealed container under ambient conditions. All packaging complies with chemical safety regulations, ensuring protection from moisture and light. Appropriate labeling and documentation accompany the shipment, conforming to international transport guidelines for research chemicals. Handle with gloves and store upon receipt as directed.
    Storage Store **4-fluorothieno[2,3-c]pyridine-2-carboxylic acid** tightly sealed in a cool, dry, and well-ventilated area away from direct sunlight and moisture. Keep separate from incompatible substances such as strong acids, bases, and oxidizing agents. Use appropriate containers, label clearly, and handle with suitable personal protective equipment to avoid inhalation or skin contact. Follow all standard laboratory chemical storage guidelines.
    Shelf Life 4-Fluorothieno[2,3-c]pyridine-2-carboxylic acid typically has a shelf life of 2–3 years when stored in a cool, dry place.
    Application of 4-fluorothieno[2,3-c]pyridine-2-carboxylic acid

    Purity 98%: 4-fluorothieno[2,3-c]pyridine-2-carboxylic acid with 98% purity is used in pharmaceutical intermediate synthesis, where high purity ensures consistent yield and minimal side-product formation.

    Melting point 205°C: 4-fluorothieno[2,3-c]pyridine-2-carboxylic acid with a melting point of 205°C is used in high-temperature reaction protocols, where thermal stability permits efficient processing.

    Molecular weight 195.17 g/mol: 4-fluorothieno[2,3-c]pyridine-2-carboxylic acid with a molecular weight of 195.17 g/mol is used in small-molecule drug research, where precise dosing and calculation facilitate reliable formulation experiments.

    Particle size <20 μm: 4-fluorothieno[2,3-c]pyridine-2-carboxylic acid with particle size less than 20 μm is used in solid dispersion technology, where fine dispersion enhances dissolution rates.

    Stability temperature up to 120°C: 4-fluorothieno[2,3-c]pyridine-2-carboxylic acid with stability temperature up to 120°C is used in hot-melt extrusion processes, where chemical integrity is maintained under process conditions.

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    Certification & Compliance
    More Introduction

    Introducing 4-fluorothieno[2,3-c]pyridine-2-carboxylic acid: Manufacturing Insights and Practical Perspectives

    Experience Makes a Difference

    Walking into a reactor bay on a misty morning, the air tinged with a faint, recognizable aroma of thienopyridines, always reminds me that chemistry starts long before any customer orders a compound. For over a decade, we’ve developed and produced specialty heterocyclic acids, but 4-fluorothieno[2,3-c]pyridine-2-carboxylic acid ranks among the most technically satisfying molecules to make. Its synthesis demands careful attention to both purity and yield, tying together the science and the day-to-day craft of chemical manufacturing.

    About the Compound

    4-fluorothieno[2,3-c]pyridine-2-carboxylic acid presents a unique blend of structural rigidity and functional potential. This compound carries a fused aromatic ring, integrating both sulfur and nitrogen in a tightly organized pattern, and the fluorine atom introduces both electronic and metabolic stability. Out of all the fluorothienopyridines we’ve handled, this one stands out for how efficiently it incorporates into downstream syntheses, especially in the pharmaceutical sector where heterocycles like these underpin so many target molecules.

    We prepare commercial quantities of 4-fluorothieno[2,3-c]pyridine-2-carboxylic acid in-house, always favoring practical process controls over shortcuts. Crystallization from carefully chosen solvents, temperature gradients measured to the degree, and vigilance at every stage, allow us to keep the product’s purity consistently above industry-standard thresholds. Batch after batch, we draw on our process experience to minimize variability, watching key intermediates and confirming the tightness of each molecular step.

    Model and Specifications: Why Details Matter

    Our team doesn’t just watch numbers roll off an instrument. Every technical choice—from the sequence of fluorination to the selection of purification steps—ties right back to the hands-on realities of manufacturing. The 4-fluorothieno[2,3-c]pyridine-2-carboxylic acid we supply typically comes as an off-white solid, with purity established using high-performance liquid chromatography and confirmed by nuclear magnetic resonance. We know trace impurities can derail both exploratory and scale-up chemistry; this suits both academic researchers and process development labs aiming for defensible, reproducible work.

    Moisture content, residual solvents, and particle consistency all follow from upstream decisions. Our internal specifications allow less residual moisture than is usually seen in outsourced lots. From prior customer feedback, we know that even a slight excess in water or solvent can trip up downstream reactions or lead to unpredictable crystal forms. The real difference: having batch data in our hands every week, we can optimize for genuine end-user needs rather than just meeting a checkbox on a certificate.

    Technical Challenges and Production Wisdom

    The synthetic pathway for this compound builds on a carefully choreographed sequence: selective halogenation, cyclization, and controlled side-chain introduction. Each of these operations can veer off course if reagents degrade or mixing gets sloppy. We’ve found that trace contaminants in the precursor thienopyridines cause late-stage failures that are expensive to fix. For that reason, our operators receive quarterly training updates and real-time feedback, and we keep detailed logs on every run, not for bureaucracy but to spot subtle trends before they affect product quality.

    Yields don’t just reflect chemistry. The amount we bring out of the reactor at each cycle depends on equipment cleanliness, reagent freshness, and the vigilance of the team taking readings every few hours. In scaling up to kilogram quantities, we confronted a spike in by-product formation. Our switch to better internal standards and a revised extraction protocol cut impurities by 40 percent, and those improvements linger through every customer order. This isn’t just a matter of pride—it has tangible benefits in time saved for anyone working downstream.

    What Sets This Compound Apart?

    4-fluorothieno[2,3-c]pyridine-2-carboxylic acid’s profile isn’t just a function of its fluorine substituent. The compound’s fused ring system delivers rigidity lacking in more flexible heterocycles. Over years of collaborating with both medicinal chemists and agrochemical specialists, we’ve seen this motif drive both potency and selectivity in structure-activity studies. Unlike simple thienopyridine acids, fluorinated versions raise the bar for metabolic resistance, stalling unwanted biotransformations during pharmacological testing.

    Compared side-by-side with non-fluorinated analogs or other pyridyl-thiophene carboxylic acids, our 4-fluoro variant resists hydrolysis and oxidative degradation, and it generally affords better solubility in common organic solvents. The electron-withdrawing effect of the fluorine atom can alter hydrogen bonding or π-stacking, important factors for anyone designing binding assays or screening new analogs. These aren’t theoretical details; we field calls from formulators whose projects stalled due to unexpected degradation with less robust molecules.

    Applications: Beyond the Literature

    Most buyers have a headline use for 4-fluorothieno[2,3-c]pyridine-2-carboxylic acid. Some are working toward new kinase inhibitors or receptor-targeted drugs, and others are building more complex fused heterocycles for material science research. We’ve watched more than one client move from gram-scale exploratory work to kilogram lots when their lead candidates pan out. Each transition brings its own technical hurdles. Scaling a reaction from milligrams in a glass vial to drums in a reactor means confronting challenges you’d never see in a university lab: clumping, dust control, thermal runaway risks.

    Having our own labs lets us model these transitions ahead of time and support users with honest numbers, not marketing claims. For custom users, we've adapted the synthetic route to tune batch size or target related motifs, keeping a focus on both throughput and waste minimization. Many contract manufacturers shy away from any deviation, but running pilot reactions directly, we can respond in real time to new requests.

    One underappreciated application comes from the compound’s utility as a scaffold for further functionalization. Whether adding new substituents onto the thiophene ring or building advanced ligand structures, starting from a fluorinated core gives chemists a shortcut through the usual maze of protecting groups and late-stage modifications. This means less time spent troubleshooting, more time on productive synthesis.

    Lessons Learned in Real-World Supply

    Every shipment we send out represents weeks of upstream planning. Weather delays, global logistics bottlenecks, and raw material pricing all affect what arrives on a scientist’s bench. We’ve built relationships with raw material suppliers who understand these constraints, and we manage buffer inventories to protect against shortages that could halt a partner’s research. Pandemics, customs backlogs, and infrastructure disruptions have all tested the system, but our in-house production gives us resilience against supplier failure.

    We reject the idea of one-size-fits-all packaging. Different projects call for different container types and fill volumes. Our filling line checks each lot for contaminants invisible to standard QA, knowing that dust or fiber errors could sabotage the precise dosing used in combinatorial work. After multiple customer reports about contamination from generic containers, we overhauled our QC process and adopted higher-grade packaging, reducing customer complaints dramatically.

    Storage and transport create their own set of hurdles. This compound handles atmospheric moisture reasonably well, but we found that prolonged exposure to high humidity can alter crystal morphology. The result: dissolution rates slow unpredictably in certain solvents. Because we routinely test for these changes, we can advise clients on shelf life and recommend real-world storage practices, from desiccation to temperature control, based on lots, not theory.

    Supporting Research and Development

    The research cycle does not wait for supply chain glitches. New compound classes often need to move from bench to pilot plant with little notice. Drawing on our own pilot lines, we act as both manufacturer and technical sounding board for process changes. Chemistry teams face pressure to beat the competition—any delay in sourcing building blocks, especially those with non-standard substituents like fluorine, can break critical project timelines.

    We document process feedback, not only to satisfy regulators or external audits, but also as part of internal practice. Each technical problem encountered—whether a failed scale-up or an unexpected impurity—becomes fuel for future systems improvements. These operational refinements might not make the headlines, but over the years they’ve translated directly into higher success rates for our clients’ research programs.

    Environmental and Regulatory Considerations

    In specialty chemical production, regulatory adherence is not negotiable. Handling fluorinated intermediates brings a particular responsibility, not just for process safety but also for downstream impact. Waste streams containing organofluorine residues demand careful segregation and traceability. We’ve invested in treatment installations and continuously retrain staff to identify deviations before they leave the plant, not after.

    International shipments trigger compliance with REACH and other framework regulations. Years of repeat audits have shown us that documentation is not just paperwork; missing detail at the source can permanently block global supply. We keep near-daily contact with compliance teams and share information openly, building a reputation for trustworthiness that outlives any single purchase. This openness translates to smoother project goals for the labs relying on our products.

    Our production lines use solvent recycling and closed-loop systems wherever feasible. We subject waste and effluent to a regular audit trail, seeking ways to minimize total environmental impact. Sharing these details with interested customers has become second nature, especially as end-users increasingly face sustainability audits from their own stakeholders. The result isn’t perfection, but it is measurable progress year after year.

    Solving Problems in the Field

    We see real value in tackling customer difficulties head-on. More than once, a client has called about low conversion rates in a coupling reaction, only for us to track the issue back to a previously unreported trace contaminant in raw materials sourced from elsewhere. Each case leads to new QC checkpoints and, if needed, a tweak in process to shed contaminants—a cycle that benefits both our operation and the broader community that uses our compounds.

    Certain projects require large quantities delivered over staggered timelines. Instead of treating each batch as isolated, we track lot histories and proactively schedule runs to match foreseeable demand. During a recent project spike, we set up an accelerated synthesis program, running dedicated shifts over weekends and evenings, ensuring the partner met their clinical trial enrollment window. That sort of flexibility can't come from intermediaries; it requires manufacturer-level control and a culture of transparency.

    Collaborative Development and Future Direction

    Manufacturing specialty building blocks encourages us to keep learning. Working directly with research leaders—from startup biotechs to global pharmaceutical teams—keeps us tuned to emerging needs. Feedback loops run both ways. Process tweaks prompted by a medicinal chemist last year might shape how we handle a batch for a materials science lab in the following season.

    Our commitment to real-world quality beats textbook reproducibility every time. We continue refining purification techniques, investing in instrumentation that gives earlier warning of trouble, and sharing our findings internally so the whole team benefits. The same standards apply to small custom runs as to bulk contracts—each molecule is checked, rechecked, and tested again to match final requirements, not just to pass a certification scan.

    Conclusion: Value Through Experience

    There’s an old adage among bench chemists: “No batch survives first contact with production.” That has shaped our philosophy from the start. Each kilogram of 4-fluorothieno[2,3-c]pyridine-2-carboxylic acid we supply carries not just a chemical structure, but the cumulative lessons of problem-solving, hands-on vigilance, and a steady drive to do better at every stage. The value customers derive from this compound reflects all the expertise and care that went into its making—translating not just into purity or yield, but into the kind of reliability that lets research and development move forward at full speed.