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3-Fluoro-4-(4,4,5,5-Tetramethyl-[1,3,2]Dioxaborolan-2-Yl)Pyridine

    • Product Name 3-Fluoro-4-(4,4,5,5-Tetramethyl-[1,3,2]Dioxaborolan-2-Yl)Pyridine
    • Alias 3-Fluoro-4-pyridylboronic acid pinacol ester
    • Einecs 816-126-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    168285

    Productname 3-Fluoro-4-(4,4,5,5-Tetramethyl-[1,3,2]Dioxaborolan-2-Yl)Pyridine
    Casnumber 864661-50-3
    Molecularformula C11H15B FNO2
    Molecularweight 221.05
    Appearance White to off-white solid
    Purity Typically >97%
    Boilingpoint Decomposes before boiling
    Solubility Soluble in organic solvents such as DMSO, dichloromethane
    Storagecondition Store at 2-8°C, protected from moisture
    Smiles CC1(C)OB(B2=NC=CC(F)=C2)OC1(C)
    Inchi InChI=1S/C11H15BFNO2/c1-10(2)15-12(16-11(10,3)4)9-6-5-8(13)7-14-9/h5-7H,1-4H3
    Reactivity Reacts with electrophiles in Suzuki–Miyaura cross-coupling

    As an accredited 3-Fluoro-4-(4,4,5,5-Tetramethyl-[1,3,2]Dioxaborolan-2-Yl)Pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 5 grams of 3-Fluoro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)pyridine, with tamper-evident seal and detailed labeling.
    Shipping This chemical, 3-Fluoro-4-(4,4,5,5-Tetramethyl-[1,3,2]Dioxaborolan-2-Yl)Pyridine, is shipped in secure, airtight packaging under ambient conditions. Shipping complies with all relevant safety and regulatory standards. Proper labeling and documentation accompany each shipment to ensure safe handling and transport, typically dispatched via ground or air freight depending on the destination.
    Storage 3-Fluoro-4-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)pyridine should be stored in a tightly closed container, under an inert atmosphere (such as nitrogen or argon), away from moisture. Store it in a cool, dry, and well-ventilated area, protected from light and heat sources. Avoid contact with oxidizing agents. Always follow chemical safety protocols when handling and storing this compound.
    Application of 3-Fluoro-4-(4,4,5,5-Tetramethyl-[1,3,2]Dioxaborolan-2-Yl)Pyridine

    Applications of 3-Fluoro-4-(4,4,5,5-Tetramethyl-[1,3,2]Dioxaborolan-2-Yl)Pyridine in Industrial Manufacturing

    3-Fluoro-4-(4,4,5,5-Tetramethyl-[1,3,2]Dioxaborolan-2-Yl)Pyridine serves as a specialized intermediate across demanding pharmaceutical and agrochemical syntheses, enabled by its boronic ester group and fluoropyridine structure. Below we outline the primary industrial segments utilizing this compound, focusing on real-world manufacturing practices and regulatory guidelines.

    1. Small Molecule API Synthesis: Antineoplastic Agents

    Pharmaceutical manufacturers employ this boronic ester as a critical coupling partner in Suzuki-Miyaura cross-coupling reactions, especially within the multistep synthesis of heterocyclic scaffolds found in innovative anticancer APIs. The controlled introduction of the fluoropyridine motif enables targeted activity against specific kinase pathways, frequently used in novel oncology pipeline drugs. Batch process control focuses on impurity management and reproducibility of the coupling reaction, essential to achieve regulatory compliance.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP, EP, JP monographs for oncology APIs
    • FDA 21 CFR Part 211 (CGMP for finished pharmaceuticals)
    • EMA Guideline on Development and Manufacture of Drug Substances

    Typical usage ratio

    • Coupling reactions typically use 1.05–1.2 molar equivalents relative to halogenated intermediates; adjustment based on reagent reactivity and impurity profile in scale-up trials.

    Downstream process integration

    • Introduced during interim stages for C–C bond formation; strictly handled in inert atmosphere reactors to avoid hydrolysis; product isolated by crystallization or preparative chromatography before downstream modifications.

    Final product types

    • Targeted kinase inhibitors (oral/IV anticancer medication)
    • Preclinical research candidates for molecularly targeted therapies
    • Reference standards for analytical laboratories

    2. Agrochemical Active Ingredient Development

    Crop protection manufacturers incorporate this compound as a building block for novel fluorinated pyridine herbicides and fungicides, where the functional groups confer increased metabolic stability and improved spectrum of activity. Coupling steps require careful process optimization to control yield and residual solvent levels, especially to meet downstream environmental and product registration requirements.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP) for test substances
    • FAO/WHO specifications on pesticide formulation
    • EPA 40 CFR Part 158 (Pesticide Registration)
    • REACH Regulation (EC) No 1907/2006

    Typical usage ratio

    • Reaction feed: 0.9–1.1 molar equivalent, fine-tuned based on target pyridine formation and process cost-efficiency during pilot and commercial scale.

    Downstream process integration

    • Added directly to cross-coupling reactors; boronic ester is consumed in the arylation stage, after which hydrolysis and formulation occur to yield the technical concentrate.

    Final product types

    • Technical herbicide actives (bulk ingredient for formulation)
    • Fungicidal intermediates for resistance management products
    • Analytical reference standards for active content verification

    3. Pharmaceutical Research: Fragment-Based Drug Discovery

    Biotech research divisions and CROs use the compound in fragment libraries for hit identification and structure-activity relationship (SAR) studies, leveraging its boronic ester functionality and fluorine for improved binding affinity in target screening assays. Throughout the synthesis, chemists monitor purity and residual solvents to conform with early-stage safety assessments and sample traceability requirements when transferring hits to lead optimization programs.

    Industry compliance standards

    • ISO 9001:2015 for research chemical quality systems
    • OECD GLP for early pharmacological testing
    • Regulatory guidelines on sample chain of custody (FDA/EMA)
    • WADA (World Anti-Doping Agency) restrictions for research chemicals

    Typical usage ratio

    • Fragment-based syntheses: typically 1.0 equivalent, with surplus based on scale and parallel syntheses to generate combinatorial libraries for screening campaigns.

    Downstream process integration

    • Integrated early in library build-up; coupled to halogenated fragments via transition metal catalysis, followed by purification for solubility testing and biological assay sample preparation.

    Final product types

    • Fragment screening panels for high-throughput screening
    • Lead-like compound sets for SAR exploration
    • Tool compounds for structural biology

    4. Custom Synthesis: Fine Chemical Building Blocks for Advanced Material Science

    Producers of organic electronic materials utilize the molecule in the modular synthesis of functionalized heterocyclic compounds designed for application in OLEDs and other electronic devices. The boronic ester facilitates palladium-catalyzed cross-coupling steps, crucial for tailoring photophysical and electronic properties. Strict QC ensures the trace metal and residual boron content comply with performance specifications for device fabrication.

    Industry compliance standards

    • ISO 9001 for chemical manufacturing
    • Internal QC specifications on trace metals (ICP-MS analysis)
    • ROHS Directive (2011/65/EU) for restricted substances in electronics
    • Material supplier qualification standards per IEC 61249

    Typical usage ratio

    • Palladium-catalyzed coupling: 1.0–1.3 molar equivalents, modified per the electronic performance criteria and purification efficiency in pilot plant optimization.

    Downstream process integration

    • Feeds into arylation stages for the generation of high-purity ligands and functionalized moieties; followed by chromatographic separation and solvent exchange for downstream thin-film deposition.

    Final product types

    • OLED emitter precursors
    • Functionalized pyridinyl intermediates for organic semiconductors
    • Reference standards for analytical device fabrication studies
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    Certification & Compliance
    More Introduction

    3-Fluoro-4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridine: Field Insights from the Production Floor

    Precision in Chemical Manufacturing: A Daily Craft

    Every morning in the plant starts with a careful check of reactor conditions, confirming temperature controls and solvent inventories before we move onto more technical batches. Among the many building blocks we produce, few demand the precision and know-how like 3-Fluoro-4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridine, known around our facility as a reliable intermediate for pharmaceutical and agrochemical labs. Crafting this molecule means more than blending the right starting materials. Each phase of this compound’s journey—sourcing, transformation, final purification—calls for thoughtful engineering decisions and years of hands-on troubleshooting. We know from first-hand experience how a slight inconsistency in boronic ester reagents or an overlooked trace of moisture during coupling can complicate the whole batch.

    In-House Knowledge Fuels Stronger Product Quality

    We have seen research teams depend on material consistency when scaling up new active candidates or discovering unusual bioactive moieties. Pyridine boronic esters get their reputation the hard way: by putting up with complex organometallic syntheses, repeated handling, and, sometimes, demanding purification steps under tight deadlines. Our choice to manufacture this pyridine boronic ester ourselves, right down to managing our own sourcing of starting fluoropyridines and pinacol, gives better control over the outcome. We track the lot’s GC-MS fingerprints, moisture content, melting point, and purity at every stage—not one batch leaves the plant before it hits our standards.

    Model Details and Batch Behavior

    Our batches of 3-Fluoro-4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridine conform to the proven molecular structure: a fluorine substituent at position 3 of pyridine and a dioxaborolane moiety at position 4. The dioxaborolane ring, held together by pinacol-derived methyl groups, delivers useful solubility and air-stability compared to unstable boronic acids or cheaper pyridine analogs. During workup, we focus on maintaining this protection, with practical measures like nitrogen blanketing and rapid filtration. Seasonal shifts in ambient humidity are a real headache for moisture-sensitive intermediates, so our staff adjusts protocols for drying glassware, vacuum-sealing, and storage in real time. These are the details that can tip a batch into high performance—or trouble.

    Traceless Functionality for Medicinal Chemistry

    Medicinal chemistry teams run Suzuki-Miyaura couplings almost daily, searching for new heterocyclic frameworks and functionalized pyridines that promise metabolic stability or improved potency. The fluorinated pyridine core in our product meets a sweet spot for selectivity in many cross-coupling protocols, favoring high yields and minimal side products. Our material, produced under reproducible conditions, meets strict HPLC and NMR characterization. Impurities, like residual pinacol or halogenated side products, can poison catalysts or gum up downstream steps. Several times, collaborating labs have traced stubborn Suzuki failures to off-spec boronic esters from generic suppliers. When the structure contains electron-donating alkyl groups in the pinacol ring, the resulting stability pays off during tedious catalyst optimization studies. Since our process keeps extraneous acid or water content in check, each flask builds trust among scale-up chemists and pilot plant staff.

    What Sets Our Process Apart

    A factory’s reputation grows from decades of technical decisions: We choose meticulously cleaned reactors, easy-to-monitor process controls, and routine recalibration of analytical tools. Years back, we struggled alongside customers who received uneven lots from mass-market distributors—some with dark coloration, others prone to rapid hydrolysis or forming sticky residues during solvent exchanges. We responded by targeting a finely controlled crystallization and handling window, avoiding thermal degradation or polymer formation. In our experience, the performance gap between materials made in-house and those packed by traders appears most stark during preclinical synthesis runs: colorimetric impurities, inconsistent melting points, or persistent solvent aromas haunt less careful supply chains. Our team takes personal pride when researchers share feedback about efficient catalyst turnover and cleaner work-ups, attributing it to reliable upstream intermediate quality.

    Application Insights: From Bench to Kilo-Scale

    In our workshops, project chemists share stories about the bottlenecks caused by simple batch variation—extra hours wasted on repeated filtrations, solvent-driven hydrolyses, or unexplained TLC artifacts. Our pyridine boronic ester, built with strict moisture exclusion and robust filtration, frees these teams from crude product reprocessing. One team reported a breakthrough in a library campaign targeting kinase inhibitors after switching to our material, which reliably dissolved in both DMF and toluene, bypassing old issues with precipitation and resin fouling. Several agricultural chemical clients have flagged the fluoropyridine motif as a durable handle for cross-coupling, introducing elemental diversity and electronic modulation into crop protection actives. These practical wins drive our drive for performance over specification-sheet showmanship.

    Making High-Value Synthesis Predictable

    Experience on the plant floor is full of minor emergencies: pump failures, heater glitches, unpredicted lot variability in precursor materials. What has made the difference in our production of fluoropyridine boronic esters is redundancy at every critical control point. We double-check the purity of solvents, adjust inerting routines daily, and run regular micro-analyses for trace halide or heavy metal contamination. Failing to keep ppm levels of these impurities low can derail gram-scale cross-couplings, forcing medicinal chemistry teams to rerun overnight reactions or troubleshoot product isolation. More than one partner organization has returned to us, months after a successful scale-up, looking for continuity in their campaigns because the output simply delivers as promised, week after week.

    Lessons from Material Failures

    Several years ago, we received analytical complaints from a contract research organization struggling to achieve full conversion in a pilot-scale Suzuki-Miyaura optimization. Their first fill had come from a generic distributor, and GC-MS analysis later showed significant oxidized byproducts, together with elevated pinacol. Burdened by repeated washes, they reached out asking for a more consistent source. Our on-staff chemists walked through the failed experiment step by step, inspected NMR traces for impurity fingerprints, and pinpointed an uncharacteristic hydrolysis event that could’ve originated during shipment from overseas. Since then, we routinely test each lot for shelf-stability, temperature sensitivity, and water uptake, publishing actual trace analyses with each drum. It’s not rare for us to pick up the phone to discuss unexpected project shifts or modification needs with our partners, ensuring a tailored fit, not just a generic fill.

    Why This Boronic Ester, Not Others?

    Competitors sometimes market cheaper, less rigorous analogs of pyridine boronic esters, with little fanfare paid to impurity profiles or authentic process knowledge. Our 3-fluoro-4-boronated pyridine stands out in areas where micro-scale side reactions transform to macro-level performance failures. The dioxaborolane ring grants stability in open air and resistance to base-catalyzed breakdown, which helps during storage in humid climates or when transferring aliquots between labs. Unlike phenyl or simple alkyl boronic esters, the electronic features of this compound—its fluorine atom and heterocyclic backbone—allow precise tuning of cross-coupling reactivity and selectivity. Our in-plant protocols, tuned to suppress trace water and minimize exposure to light or heat, mean chemists can lean on each delivery for long-haul syntheses or multi-step routes spanning several months.

    User Feedback: A Two-Way Street

    Each time our team packs up a shipment for a new or returning partner, feedback cycles come full circle. Several regular users flag differences against competitors’ materials—our product re-dissolves cleanly after refrigeration, retains color and clarity across seasonal swings, and sharply reduces background product noise in NMR runs. Process support teams face fewer troubleshooting calls regarding unexpected by-products or loss of yield. Direct communication with end-users keeps our approach practical and responsive, with regular improvements in packaging, delivery timing, and real-time data sharing. Rather than chasing quarterly volume targets, we value long-standing relationships built on daily, boots-on-the-ground engagement.

    Continuous Improvement, Not Just Compliance

    Day-in, day-out, watching reactors fill, filter beds tighten, and rotavaps hum, our staff keeps notes on variables that textbooks don’t cover: shifts in dust levels at raw material unloading bays, unexpected corking during filter cake breaks, and even slight color shifts in solvent drums after abrupt weather changes. These small observations, logged and shared in morning meetings, find their way into process tweaks that keep each batch of 3-Fluoro-4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridine consistent and robust. No checklist replaces the kind of judgment earned from seeing edge-cases in pilot runs and scale-ups. We view regulatory audits not as the finish line, but as a springboard for deeper investigation and process hardening. Trust grows from repeated demonstrations of control, not from paperwork alone.

    Security of Supply and Documentation: Building Confidence

    Global events—from severe weather to unforeseen shipping delays—regularly test just-in-time supply chains. Our on-site stock of key fluorinated pyridine and pinacol intermediates acts as a buffer against long lead times, ongoing logistics volatility, and vendor reliability gaps. Proactive planning around critical path material ensures continuity even during regional disruptions. Reliable batch-to-batch traceability extends to every drum of boronic ester shipped, supported by full COA data, NMR, and GC-MS prints. Partner labs and manufacturers check these data sets before starting costly syntheses, and, if needed, reach our technical support for direct troubleshooting. That kind of transparency, combined with practical access to technical staff, cements the foundation for productive, repeatable collaboration between producer and user.

    Adaptation: Supporting Evolving Chemistries

    Over the years, our production line has evolved as synthesis trends shift in the pharmaceutical and crop science industries. Some years, the call for low-halogen intermediates or specific fluorination patterns picks up; other times, regulatory changes around hazard labeling prompt reformulation of packaging and shipment. Our labs stay tuned to these shifts, sometimes rerouting product directly to early-stage research partners deploying new reaction conditions or support formats. Flexibility is our strength: We have carried out custom lot fractionation, supported alternative drying regimens, even tested inert liners or light-proof packaging for especially sensitive programs. The feedback gained from these adaptations serves as a practical knowledge base for the next application or custom request, reinforcing the value of manufacturing depth over trading desk solutions.

    Comparing Real-World Differences

    Talk travels quickly among research groups about which suppliers' materials work without fuss and which require workarounds. The balance of electronic effects in our 3-fluoro-4-boronated pyridine means cross-couplings run at milder temperatures and with lower catalyst loads, freeing up budget and time. One medicinal chemistry group commented that by switching to our in-house batches, they not only improved reproducibility but also avoided buying larger volumes to compensate for unpredictable yields. Other users find downstream purification simpler, with fewer colored impurities or sticky residues, thanks to the stricter headspace and filtration steps we follow in the plant. Most notable is the reduction in “invisible downtime”—time not captured on project trackers—spent debugging reactions or re-running faulty syntheses. These real-world benefits don’t always show up in technical bulletins but resonate in everyday lab conversations.

    Shared Success: Building More Than Molecules

    Inside the manufacturing plant, every operator, process chemist, and technician shares responsibility for keeping the product line robust and reliable. The pride in a clean chromatography trace, a shelf-stable drum, or an endorsement from a trusted project partner forms the heart of our work ethic. We see the daily realities of chemical synthesis as a partnership built on real experience, stretching from raw material bins to final QC sign-off. This collaborative approach carries through every batch of 3-Fluoro-4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridine we produce, supporting the collective progress of innovation in labs and industries around the world.