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5-Fluoro-2-Methoxycarbonylphenylboronic Acid

    • Product Name 5-Fluoro-2-Methoxycarbonylphenylboronic Acid
    • Alias 5-Fluoro-2-methoxycarbonylphenylboronic acid
    • Einecs 841-524-8
    • 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

    239514

    Productname 5-Fluoro-2-Methoxycarbonylphenylboronic Acid
    Casnumber 864377-76-4
    Molecularformula C8H8BFO4
    Molecularweight 197.96
    Appearance White to off-white solid
    Meltingpoint Approx. 180-185°C
    Purity ≥ 97%
    Solubility Slightly soluble in water, soluble in organic solvents
    Storagetemperature 2-8°C
    Smiles B(C1=CC(=C(C=C1)F)C(=O)OC)(O)O
    Inchikey IZFJAEDWSLOPCG-UHFFFAOYSA-N

    As an accredited 5-Fluoro-2-Methoxycarbonylphenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass vial containing 1 gram of 5-Fluoro-2-Methoxycarbonylphenylboronic Acid, sealed with a tamper-evident cap and labeled.
    Shipping 5-Fluoro-2-Methoxycarbonylphenylboronic Acid is securely packaged to prevent moisture or contamination during transit. It ships in sealed, inert containers, typically under ambient or cool conditions. Compliance with chemical shipping regulations ensures safe handling. Expedited and tracked delivery options are available, accompanied by a material safety data sheet (MSDS) upon request.
    Storage 5-Fluoro-2-Methoxycarbonylphenylboronic Acid should be stored in a tightly sealed container, protected from light and moisture. Keep it at 2–8°C (refrigerated) in a well-ventilated, dry area designated for chemicals. Avoid contact with incompatible substances, such as strong oxidizers. Ensure appropriate labeling and compliance with chemical safety regulations for storage and handling.
    Application of 5-Fluoro-2-Methoxycarbonylphenylboronic Acid

    Applications of 5-Fluoro-2-Methoxycarbonylphenylboronic Acid in Industrial Manufacturing

    As a manufacturer directly producing 5-Fluoro-2-Methoxycarbonylphenylboronic Acid, we supply this arylboronic acid intermediate primarily for advanced synthesis in pharmaceutical and agrochemical industries. Its performance in Suzuki-Miyaura cross-coupling, precision aromatic substitution, and molecular modification drives several downstream applications. This page outlines verified industrial use cases, technical parameters, and compliance requirements addressed by our manufacturing standards.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Oncology Compounds

    Our material serves as a key building block in the targeted synthesis of fluorinated small molecules used in the development of kinase inhibitors and related anti-cancer therapeutics. Pharmaceutical processors employ this intermediate during the assembly of complex aromatic frameworks in heterocyclic drug candidates, where regulatory control over purity and process validation is paramount to downstream approval.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • EU-GMP (EudraLex Annex 1 & 13)
    • United States Pharmacopeia (USP) standards for residual solvents and impurities
    • FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)

    Typical usage ratio

    • 0.8–1.2 molar equivalents in Suzuki coupling steps, scaled with target batch size and adjusted by analytical monitoring of conversion

    Downstream process integration

    • Introduced post-halogenation, during the palladium-catalyzed cross-coupling operation for biaryl bond formation in stepwise synthetic routes

    Final product types

    • Investigational and commercial oncology APIs (e.g., fluorinated kinase inhibitors, heterocyclic anti-tumor agents)
    • Advanced pharmaceutical intermediates for subsequent heteroatom derivatization

    2. Agrochemical Active Ingredient Synthesis

    Crop protection companies utilize this compound in laboratories and pilot plants for the assembly of fluorinated phenyl moieties within selective herbicide and insecticide candidates. Its electronic properties facilitate functionalization at defined positions, a requirement in the generation of molecules for resistance management formulas.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (analytical and purity requirements)
    • REACH Regulation (EC) No 1907/2006 (registration and safety compliance)
    • ISO 9001:2015 (Quality Management Systems for chemical manufacturing)
    • OECD Guidelines for the Testing of Chemicals (for environment and human health impact assessment)

    Typical usage ratio

    • 0.95–1.05 molar equivalents for coupling with halogenated precursors, with stoichiometry adapted to target conversion and minimal boron residue in technical grade synthesis

    Downstream process integration

    • Applied during stepwise Suzuki-Miyaura coupling in multi-stage synthetic processes; used after initial ring construction for final aryl diversification

    Final product types

    • Technical grade agrochemical actives (e.g., new-generation trifluoromethyl herbicides, phenyl-fluorine insecticidal agents)
    • Patentable experimental crop protection compounds for greenhouse/field trials

    3. Advanced Material Science – Functional Polymers and OLED Intermediates

    Manufacturers of electronic material and specialty polymers employ this boronic acid derivative to introduce fluorinated aromatic sequences into polymer backbones, optimizing charge mobility and light-emitting properties for advanced optoelectronic devices. Strict control of contamination and side-reactions is required due to high-performance demands.

    Industry compliance standards

    • RoHS Directive (Restriction of Hazardous Substances in Electrical and Electronic Equipment)
    • IEC 62321 (Methods for the determination of certain substances in electrotechnical products)
    • ISO 14644-1 (Cleanroom and associated controlled environments)
    • Customer-specific QMS requirements for electronic grade chemicals

    Typical usage ratio

    • 0.6–1.0 equivalent per aromatic halide monomer, depending on desired substitution density in copolymer or oligomer product

    Downstream process integration

    • Added during monomer coupling stages for polyfluorinated phenylene or biphenylene synthesis via transition metal catalysis; polymerized under controlled atmosphere conditions

    Final product types

    • High-performance resins for OLED emissive layers
    • Engineering plastics with tunable dielectric/magnetic properties
    • Display-grade functional polymers for organic electronics applications

    4. Custom Fine Chemicals for Research and Pilot-Scale Synthesis

    Specialty chemical companies and pilot research labs order this boronic acid intermediate for the assembly of advanced structures used in the synthesis of drug lead compounds and reference standards. Its selectivity and adaptability make it valuable in multiple proprietary synthetic routes, requiring traceable analytical data and controlled handling during new chemical development.

    Industry compliance standards

    • ISO 17025 (General requirements for the competence of testing and calibration laboratories)
    • OECD Good Laboratory Practice (GLP) for chemical synthesis and analysis
    • Specific client protocols for chemical provenance and documentation (e.g., Certificate of Analysis, batch traceability)
    • Local and international hazardous materials handling and transportation regulations (GHS, IATA, ADR)

    Typical usage ratio

    • Typically 1.0 equivalent in small-molecule coupling reactions; subject to further optimization based on structure-activity relationship screening or analytical requirements for target molecules

    Downstream process integration

    • Serves as a core reactant during late-stage diversification of aromatic systems, generally under inert atmosphere and low-metal contamination protocols for fine chemical R&D syntheses

    Final product types

    • Synthetic reference standards for analytical development
    • Advanced research intermediates for custom pharmaceutical or material innovation
    • Screening libraries for drug discovery programs
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    Certification & Compliance
    More Introduction

    Product Commentary: 5-Fluoro-2-Methoxycarbonylphenylboronic Acid

    Real-World Manufacturing Insights

    Direct work with 5-Fluoro-2-Methoxycarbonylphenylboronic Acid never feels routine. We understand this compound’s growth in demand reflects a deeper trend in synthetic organic chemistry. Working in the factory every day, we have seen both excitement and pressure around improvements to aryl boronic acid building blocks, especially those combining a fluorine atom with a methoxycarbonyl group on the phenyl ring. In our experience, such dual functionalization creates opportunities for medicinal and materials chemistry that simpler variants do not offer.

    Structure Matters: Properties Shaped by Synthesis

    Our own batches of this boronic acid regularly meet strict performance expectations that basic phenylboronic acid products cannot reach. The fluorine substituent at position 5 strengthens the arene’s electronic properties, while the methoxycarbonyl at position 2 fine-tunes reactivity with coupling partners. These features aren’t only theoretical advantages; chemists in process scale frequently tell us this structure delivers better selectivity, higher product yields, and more robust downstream chemistry compared to non-fluorinated or non-ester analogs. From our reactor vessels to the final QC bench, small changes in our conditions—temperature, base selection, quenching technique—show clear impacts on the boronic acid’s integrity and shelf life. Reproducibility, once a challenge, now defines each production lot, even as our capacity ramps up.

    Applications Driving the Need

    Requests for this compound nearly always trace to advanced Suzuki-Miyaura coupling projects. As fluoro-aryl boronic acids have become more popular with researchers and process chemists, this product’s mix of reactivity and versatility stands out. Feedback from pharmaceutical labs points to its value in rapid library generation—enabling quick exploration of structure-activity relationships in small-molecule programs. The conversation rarely stops at the API intermediate stage, either. Teams working on new OLED materials, agrochemical leads, or even specialty polymers describe how they use the unique electronics of our product to push their chemistry into new regimes.

    From a manufacturing standpoint, it is easy to understand why others struggle to consistently produce this compound at scale. Unwanted byproducts form when conditions are off by as little as a few degrees. Fine particulate matter fouls filtration unless handled with practiced precision. We routinely analyze for sub-millimole impurities, feeding our process improvement cycles and learning from every deviation, no matter how minor.

    What Sets 5-Fluoro-2-Methoxycarbonylphenylboronic Acid Apart

    Having worked with a wide spectrum of boronic acids, there is a tangible difference as soon as you handle this one on the production floor. The crystalline texture, melting behavior, and robust color distinguish it from simpler boronic acids, and the mild but unique aroma comes from the ester function—never present in the common 4-fluorophenylboronic acids or in phenylboronic acid itself. Our QA sampling regime detects slight moisture sensitivity in some lots, so we treat storage and packaging conditions as a process step, not an afterthought.

    We compared our own product to both domestic and imported samples. Many overseas competitors use routes that leave trace metal contaminants or fail to drive the coupling precursors to completion. Several partners have told us that side reactions plague these alternatives, slowing their own downstream operations and creating headaches for their analytical teams. It is not unusual for partners to request re-supply within weeks after "trying to make do" with off-the-shelf alternatives. This is a story we hear repeatedly.

    Within our own facility, analytic data shows that our process can suppress most typical byproducts, including those that result from boronic acid dimerization or incomplete transesterification. Every time we tighten process control, customer reports reflect cleaner HPLC traces and more reliable uptake into finished target molecules.

    Serving Evolving Industry Demands

    Every trend in modern organic synthesis points toward higher expectations for building block quality and functionality. The steady expansion of fluorinated scaffolds in pharmaceutical and materials discovery means specialty boronic acids like this have moved from being rare curiosities to foundational reagents. Our plant team meets researchers at the bench and pilot plant, not as vendors but as partners—discussing yield impacts, isolation strategy, and risk control. We share concerns about cost pressure and efficiency: no researcher wants to waste time troubleshooting a coupling failure caused by a trace impurity.

    Our clients tell us that the 5-fluoro group often pushes target molecules into new solubility regimes or tunes them for better biological activity, while the methoxycarbonyl eases integration with downstream derivatizations. These are properties you can't fake post-synthesis—we have to build them into the molecule from the start. As new reaction types emerge, the tolerance windows for isomeric purity and moisture stability keep narrowing. To keep up, we have scaled up internal analytics and process monitoring beyond what regulatory minimums require, because practical reliability counts as much as any certificate.

    Quality Rooted in Day-to-Day Operations

    Producing 5-Fluoro-2-Methoxycarbonylphenylboronic Acid is not a simple extension of making generic boronic acids. Sourcing pure 5-fluoro-2-methoxycarbonylbenzene precursors forces us to trace every fine impurity in our supply chain. Tubing and reactor lines need frequent inspection; the acidic and basic phases run at temperatures that encourage polymeric residues. Clean-out is hands-on work—no robot or simple solvent flush can substitute the vigilance of skilled operators tracking pressure and color changes shot-by-shot.

    Shipment batches are not just signed off by quality assurance—they are subject to real-life stability challenges. We have seen how neglecting moisture and light control can transform brilliant crystalline powder to a sticky solid, even under what look like normal storage conditions. And once packed for transport, we have logged the effects of air shipment delays and storage in non-temperature-controlled facilities. Long-term buyers use this information to set up their own storage and dispensing protocols; our technical service teams discuss these details openly, going well beyond what a spec sheet provides.

    Supporting Next-Generation Synthesis

    Discussions with contract chemists highlight how this molecule regularly broadens options during complex multi-step syntheses. Diaryl compounds and heterocyclic intermediates get assembled faster thanks to this boronic acid’s reactivity profile. Process chemists trying to avoid halogen exchange or heavy metal leaching benefit from its cleaner coupling outcomes. In pilot scale runs, our partners say process throughput improves because the product dissolves and reacts more predictably than related compounds. Each cycle spent in optimization uses up not only material, but time and morale—something every plant manager knows counts double on a deadline.

    We have worked with university groups who rely on our technical support to adapt batch parameters. In publishing new ligands or screening arrays, they want predictable and clean starting points. Sometimes these projects push temperature or pH into margins beyond standard procedures. We track their outcomes, record setbacks, and often bring changes back to our own reactor setups. The mutual feedback loop between bench and production improves the molecule batch-by-batch, year over year.

    Common Challenges and Our Solutions

    Our facilities have encountered the unique issues arising from the presence of both fluorine and a carboxylate ester in the same ring. Cross-contamination from non-fluorinated chemical lines leads to subtle but real product quality declines, so we dedicate production reactors to this family of molecules. Cross-checking between production and QC tightens accountability within teams. Failures, rare as they are, receive immediate root-cause investigation—whether the problem came from a process deviation, raw material, or equipment failure.

    The market for boronic acids includes a wide spread of price and quality points. We could take shortcuts and push lower purity grades at commodity costs, but experience shows this undermines trust with our application chemists. Batches that skip thorough control lose appeal after just a few trial runs. We invest in screening and collaborative troubleshooting, done well before product launch. Data on moisture, residual solvents, and sub-milligram contaminants are logged and referenced as often as melting point and chromatography.

    Why This Boronic Acid Matters to the Industry

    Chemical manufacturers like us often operate behind the scenes, yet the value this product brings becomes obvious in the hands of our partners. When a medicinal chemist can confidently scale a reaction and nail the analytics on the first try, the project accelerates. We see our product in patents, regulatory filings, and even in the glassware of start-ups taking their first steps in discovery. Each application story circles back to the fundamental strength of this compound’s molecular design and the way we grew to manufacture it without compromise.

    While some companies focus only on molecular structure, ignoring impurities or byproduct traces, our daily routines keep process discipline and end-user context tied together. Each drum or gram leaves our plant only after thorough scrutiny, because experience shows flaws multiply downstream if ignored upstream.

    The Next Phase: Continuous Improvement and Responsibility

    Practical realities on the factory floor keep us alert to the changing requirements of the chemical industries we support. As new sustainability standards and digital tracking tools emerge, we update our practices—not to chase certifications, but because waste reduction and batch traceability make daily operations easier and safer for everyone. Analytics run during each shift now feed directly to process historians, flagging any risk point for corrective action.

    One focus area involves improving the environmental profile of our solvents and recycling streams. Boronic acid chemistry sometimes involves organics and bases that are not always easy to handle, but we experiment constantly with new scavenging and regeneration techniques. This helps keep workplace exposure low and improves long-term supply continuity.

    Worker training remains a hands-on, evolving responsibility—new hires learn by shadowing experienced staff, not just classroom instruction. Our teams discuss the strengths and limitations of each production lot, treating every deviation as a teaching opportunity. It’s this factory floor tradition, paired with high standards, that keeps improving product consistency and technical value.

    Closing Notes From Our Production Perspective

    Many trends in chemical manufacturing pass quickly, but the ongoing story of 5-Fluoro-2-Methoxycarbonylphenylboronic Acid reflects the real and persistent evolution of chemical synthesis. End users keep setting higher bars, pushing us to do more than just meet an average specification. This product stands as a result of decades of process learning, technical exchange, and teamwork across development and production. Customers notice the difference when rigorous work shows in the glassware, in the chromatography, and in every bottle that moves from plant to lab.

    We take pride in knowing our boronic acid helps researchers and manufacturers go farther, solve bigger challenges, and drive discovery. Every batch carries not only a molecular structure, but also the dedication and insight of people who know what it takes to serve science under real conditions.