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4-Methoxy-2-Formylphenylboronic Acid

    • Product Name 4-Methoxy-2-Formylphenylboronic Acid
    • Alias 4-Methoxy-2-formylphenylboronic acid
    • Einecs 841-499-7
    • 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

    950547

    Productname 4-Methoxy-2-Formylphenylboronic Acid
    Casnumber 105358-66-7
    Molecularformula C8H9BO4
    Molecularweight 179.97
    Appearance Off-white to light yellow solid
    Meltingpoint 180-184°C
    Solubility Slightly soluble in water, soluble in DMSO and methanol
    Purity Typically ≥ 98%
    Smiles COC1=CC(=C(B(OH)2)C=C1)C=O
    Inchi InChI=1S/C8H9BO4/c1-13-7-4-6(5-10)3-8(2-7)9(11)12/h3-5,11-12H,2H2,1H3
    Synonyms 2-Formyl-4-methoxyphenylboronic acid
    Storage Store at 2-8°C, protect from moisture

    As an accredited 4-Methoxy-2-Formylphenylboronic 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 5-gram amber glass bottle with a secure screw cap, labeled with product details and hazard information.
    Shipping The shipping of **4-Methoxy-2-Formylphenylboronic Acid** is conducted in compliance with regulations for chemical transport. The compound is securely packaged in sealed containers to prevent moisture and contamination. It is shipped at ambient temperature unless otherwise specified, with appropriate labeling and documentation to ensure safe and traceable delivery.
    Storage 4-Methoxy-2-Formylphenylboronic Acid should be stored in a cool, dry, well-ventilated area, away from direct sunlight and moisture. Keep the container tightly closed and store at 2-8°C (refrigerator) if possible. Avoid contact with strong oxidizing agents, and label the container appropriately. Use personal protective equipment during handling to ensure user safety.
    Application of 4-Methoxy-2-Formylphenylboronic Acid

    Applications of 4-Methoxy-2-Formylphenylboronic Acid in Industrial Manufacturing

    As a direct manufacturer of 4-Methoxy-2-Formylphenylboronic Acid, we supply this specialty boronic acid to a range of advanced industrial sectors. Below, we present distinct application areas with their real-world compliance, compositional practices, process placements, and final product outputs.

    1. Pharmaceutical API Synthesis—Aryl Boronic Acid Coupling Reactions

    API producers in the pharmaceutical industry utilize our product as a key boronic acid coupling partner in palladium-catalyzed Suzuki-Miyaura cross-coupling to construct biaryl and heteroaryl motifs. This step often appears in the late-stage assembly of small-molecule drugs where strict material traceability and impurity control remain critical. The intermediate formation and further elaboration of substituted aromatics depend directly on the high purity and reactivity profile of our raw material, especially when manufacturing kinase inhibitors and neuroactive agents. Quality systems enforce batch traceability, and process routes require documentation according to validated protocols.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF and EP monographs for relevant APIs and intermediates
    • EU GMP Guidelines Part I and II
    • FDA 21 CFR Part 211 – Finished Pharmaceuticals

    Typical usage ratio

    • 0.95–1.15 molar equivalents relative to the aryl halide, adjusted for reaction scale and kinetic profile

    Downstream process integration

    • Added to anhydrous reaction vessel during the coupling phase, immediately before base and catalyst charging
    • Monitored for residual starting material by LC-MS or HPLC throughout the coupling and work-up stages

    Final product types

    • Pharmaceutical active ingredients (e.g., kinase inhibitors, anti-tumor agents)
    • Pharmacologically active intermediates requiring boron functional group removal

    2. Agrochemical Intermediate Production—Herbicide and Fungicide Synthesis

    Top agrochemical manufacturers employ this aromatic boronic acid as a building block in the synthesis of complex heterocyclic intermediates for modern herbicides and seed-treatment fungicides. The stability and selectivity in transition-metal-catalyzed coupling reactions reduce byproduct profiles and waste, meeting process safety and environmental benchmarks required for large-scale crop protection agent manufacture. Automation in continuous reactors improves material flow and exposure management during scaling to multi-kilogram quantities.

    Industry compliance standards

    • FAO/WHO specifications for technical grade active ingredients
    • REACH Regulation (EC) No 1907/2006 for substance registration and safety reporting within the EU
    • ISO 9001:2015 for Quality Management Systems
    • Relevant OECD guidelines for testing of chemicals

    Typical usage ratio

    • 0.90–1.10 equivalents relative to the halogenated substrate; ratio optimized for target yield versus byproduct content

    Downstream process integration

    • Charged to batch or flow system following substrate dissolution and pre-catalyst charge
    • Residual boron monitored by ICP-OES prior to downstream formulation or further synthetic steps

    Final product types

    • Herbicide intermediates with aryl or heteroaryl backbones
    • Seed treatment fungicide precursors with methoxy-substituted aromatic cores

    3. OLED and Organic Electronics Materials Synthesis

    Producers of organic electronic materials integrate this compound as a pivotal C–C coupling agent during the construction of functionalized aromatic monomers and oligomers for high-performance organic light emitting diode (OLED) emissive and transport layers. The boronic acid group facilitates precise placement of aldehyde and methoxy functionalities, which directly influence emission wavelength and charge mobility in final device structures. Purity and trace metal content critically affect downstream device performance and failure rates under thermal or high-voltage load.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (for restricted use of hazardous substances in electronics)
    • IEC 62321 for determination of certain substances in electronic equipment
    • ISO 14001:2015 (Environmental Management Systems) for cleaner production

    Typical usage ratio

    • 0.95–1.05 molar equivalents per coupling position; ratios tied to monomer structure and electronic property targets

    Downstream process integration

    • Dosed at key cross-coupling point for the formation of biaryl linkages in precursor synthesis, under controlled atmosphere systems
    • Purity confirmed by GC-MS or NMR prior to purification and device fabrication

    Final product types

    • OLED emitters and transport layers (e.g., blue/yellow dyes, hole injection materials)
    • Specialty electronic intermediates for organic photovoltaic cells and thin-film transistors

    4. Fine Chemical and Specialty Dye Synthesis

    Producers of high-value specialty dyes and pigments employ our boronic acid in the synthesis of functionalized aromatic cores, where methoxy and formyl substituents influence chromophoric properties. The compound enables regioselective biaryl couplings and further derivatization to introduce solubilizing or electron-donating features, crucial in the development of new colorants for fiber, inkjet, and imaging applications. Batch documentation supports full backward traceability throughout the process.

    Industry compliance standards

    • EN 71-3:2019 (Safety of toys—Migration of certain elements, for pigment applications in children’s products)
    • OEKO-TEX Standard 100 (textile dye safety)
    • ISO 9001:2015 for Quality Management and consistent production traceability

    Typical usage ratio

    • 1.00 equivalent in cross-coupling as a terminal aryl donor; adjusted for chromophore design goals

    Downstream process integration

    • Introduced to reaction system after solvent and base setup, prior to heating and catalyst addition
    • Residual boronic acid checked by TLC or HPLC before work-up and downstream modification

    Final product types

    • Specialty dyes for synthetic fiber and textile coloration
    • Inkjet and photographic imaging colorants with aldehyde-methoxy motifs

    5. Medicinal Chemistry Research and Development

    Research teams in drug discovery, within pharmaceutical and contract research organizations, use this compound to prepare arylated libraries for SAR (structure-activity relationship) screening. Its unique electronic and steric properties influence binding in lead compound optimization, especially when developing CNS, oncology, and anti-inflammatory candidate molecules. Detailed material safety data and batch certificates support its use in validated experimental procedures.

    Industry compliance standards

    • GLP (Good Laboratory Practice, OECD Principles)
    • Internal QA/QC guidelines aligned with ICH Q3A (Impurities in New Drug Substances)

    Typical usage ratio

    • 0.90–1.20 equivalents in research-scale syntheses; ratios tailored per synthetic design and analytical requirements

    Downstream process integration

    • Charged to microscale or preparative-scale palladium coupling reactions during lead expansion synthesis
    • Purity and identity verified by NMR, LC-MS, and HPLC following each transformation step

    Final product types

    • Analytical samples of drug intermediates for SAR libraries
    • Microgram to gram quantities of candidate drug molecules
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    Certification & Compliance
    More Introduction

    Introducing 4-Methoxy-2-Formylphenylboronic Acid: A Reliable Building Block for Modern Synthesis

    Bringing Precision to Organic Synthesis

    In the field of chemical manufacturing, new synthetic challenges appear almost every month. Lab managers and process chemists look for answers that improve both the efficiency and selectivity of their protocols. As a manufacturer, experience shows us that the design and choice of reagents do most of the heavy lifting. It’s why we have committed resources to the precise production of 4-Methoxy-2-Formylphenylboronic Acid (model: MFPA-1022), which supports a range of reliable, high-fidelity transformations expected in pharmaceutical, materials, and specialty chemical synthesis.

    What Sets This Compound Apart

    Over the years, boronic acids have become central to Suzuki-Miyaura coupling and a variety of palladium-mediated cross-coupling reactions. As a manufacturer producing both common and specialized boronic acids, the difference between this compound and standard phenylboronic acid starts with its functional groups: the methoxy at the para position and the formyl group at the ortho position. This structural arrangement drives both reactivity and selectivity in advanced syntheses.

    In practical use, 4-Methoxy-2-Formylphenylboronic Acid distinguishes itself in a few clear ways. At scale, we find it is less prone to uncontrolled oxidation during storage compared to its analogs bearing other electron-donating substituents. The formyl group offers versatile points of derivatization downstream, opening up more intermediate options than simpler boronic acids, which often force a pivot in route selection mid-synthesis. Chemical engineers at our facilities have tested batches of both standard and methoxyformyl-substituted variants and consistently note improved yields in certain targeted coupling reactions.

    Production Philosophy and Quality Management

    There are reasons many R&D teams seek out 4-Methoxy-2-Formylphenylboronic Acid made by manufacturers like us, rather than relying on bulk resellers. From the earliest stages, process reproducibility and traceability matter. Our plant runs dedicated lines to reduce cross-contamination. Each lot gets full analytical support: nuclear magnetic resonance, high-pressure liquid chromatography, as well as impurity profile determination. Shifting through the years from small-batch glassware to automated batch reactors, we’ve put process controls in place to guarantee that even multi-kilogram lots maintain the expected purity and reactivity profile.

    Occasionally, customers recount issues with inconsistent melting points or suspiciously high levels of boronic anhydrides in unknown provenance material. That can mean lost time or digital scale headaches downstream. We’ve tackled these problems by refining the crystallization protocols, adjusting solvent grades, and timing the work-up better. Several contracts required our lot-to-lot reproducibility to outperform earlier suppliers, which led to further investments in on-line monitoring and tighter overhead control. Scientific rigor isn’t just for regulatory checklists—it’s about delivering a reagent that performs, batch after batch, from kilo lab to pilot plant.

    Crucial Applications and Performance in the Lab

    Chemical manufacture is as much about the people making the material as the molecules themselves. In practice, 4-Methoxy-2-Formylphenylboronic Acid shows particular strength for chemists engaged in drug discovery and late-stage functionalization. The aldehyde group offers multiple branches for subsequent transformations, such as reductive amination, Knoevenagel condensations, and even specialized imine chemistry. Many synthetic chemists value the compatibility of the methoxy group, especially when targeting heteroatom-linked frameworks for medicinal chemistry. Its electron-donating character promotes coupling under milder conditions, which can preserve sensitive protecting groups or fragile cores.

    Scale-up is where subtle differences really matter. On a bench scale, a gram of 4-Methoxy-2-Formylphenylboronic Acid looks much like any pale solid. On a 20 kilogram run, the physical stability, low dusting propensity, and the absence of clumping make handling straightforward, even under challenging humidity conditions. In our experience, this material resists hydrolysis better than some related boronic acids, especially those with more electron-rich substituents or sensitive sulfonates. Process chemists often ask about shelf life. Extended stability testing in our warehouse shows no appreciable decomposition over two years in sealed vessels, with no significant boroxine formation, provided ordinary dry storage protocols are followed.

    Among the practical hurdles in pharmaceutical manufacturing, the purification of intermediates often slows progress. Our team prioritizes boronic acids like this one because post-reaction work-ups proceed more cleanly. The methoxy and formyl groups appear to help both by reducing by-product complexity and by tuning hydrophilicity, meaning fewer column fractions and easier salt removal. In our technical service history, we’ve supported multiple clients through targeted troubleshooting when contaminants threatened to derail a project. By adjusting the isolation method, our quality team managed to drive impurity content below critical thresholds without sacrificing yield—a direct benefit of the compound’s unique chemical characteristics.

    Comparison to Other Boronic Acids

    Manufacturing and using chemically similar boronic acids exposes subtle, but often crucial, differences. Phenylboronic acid, while a mainstay, lacks the fine control over reactivity that comes with strategic substituents. For example, the classic 4-methoxyphenylboronic acid, though used widely, cannot offer the same onward transformation chemistry as our methoxyformyl analog. Conversationally, researchers share that jobs needing multiple downstream operations see a clear workflow improvement with this compound. Instead of adding formyl groups through hazardous formylation post-coupling, which can complicate purification or introduce side-products, using our product integrates these steps from the outset.

    Compared to ortho- or meta-methoxyboronic acids, the balance of electronic and steric effects leads to more predictable cross-couplings. Shelf stability stands out for this product as well. Bulk containers leaving our facility display less moisture uptake, which can translate to fewer delays in multi-step syntheses. Early experience with less optimized grades from other sources taught us to refine particle size and packaging—those modest changes cut residual moisture and enhanced reactivity in automated flow reactors. Technical leads reviewing side-by-side trial data commented that their reaction windows widened, giving process chemists more room to operate in scale-up campaigns.

    Meeting Evolving Customer Needs

    Change is a constant throughout the chemical sector. In the last decade, more industry customers have pushed for greener, more atom-economical synthesis routes. Scientists at our plant recognize the downstream implications of every reagent on waste reduction, solvent selection, and overall risk. For 4-Methoxy-2-Formylphenylboronic Acid, use in Suzuki-Miyaura and related couplings means fewer steps, which lowers both waste and variable process hazards. Once, a major pharmaceutical client shared their metrics: moving to this compound shaved a full day off their synthesis timeline, trimmed consumption of costly co-solvents, and tightened their process safety margins.

    In these practical settings, customer successes stem not only from the chemical but also the reliability behind each delivery. Our team tracks market feedback and internal analytic data, always looking for the micro-improvements that make a measurable impact. We reduced residual solvent levels across all boronic acid lines two years ago—a change prompted by customer reports about interference with sensitive active ingredients. That hands-on, iterative approach keeps us aligned with industry’s real-time needs, not just theoretical ideals. You won’t find us resting on the laurels of a single product; every batch of 4-Methoxy-2-Formylphenylboronic Acid leaves our site under the eyes of seasoned production staff, who know both the stakes and the science behind their work.

    Common Questions and Troubleshooting

    After hundreds of thousands of kilos produced, recurring application questions still come up. Some buyers wonder whether the dual reactivity of this compound—methoxy and formyl—raises challenges in particular synthetic steps. In most cross-couplings, the methoxy group stabilizes the aromatic ring, while the formyl can be protected or left open to further transformation. Chemists working on route scouting often reach out about handling and storage. Direct experience shows that contamination and hydrolysis can be minimized by using only freshly charged scoops, tightly re-sealing drums, and avoiding long-term exposure to humid air. Our technical support staff receive reports of variable reactivity in pilot plant trials using generic materials; after switching to our controlled lots, most teams report restoration of yields and smoother downstream processes.

    Every year brings requests for support in non-standard applications. Teams in electronic materials research, for example, have explored our product for incorporating electron-rich motifs in OLED precursor frameworks. Consistent particle properties and batch records mean that even small process deviations can be traced and addressed proactively. In-house analytical data, amassed from thousands of runs, forms the backbone of our troubleshooting protocols. Rather than troubleshooting in the dark, our clients benefit from supplier engagement at every stage.

    Packaging, Storage, and Sustainability Considerations

    The modern chemical industry calls for more than just high-purity chemicals; it demands respect for safe handling, environmental responsibility, and cost control. Our company uses tight-seal, moisture-resistant containers sized for typical batch feeds. Years ago, a shift to this packaging format markedly reduced user complaints about caking or product loss. Warehouse technicians track shelf life with monthly stability pulls. Internal audits check for early evidence of degradation or shifts in melting behavior. We record all these parameters, with traceable links to each production run.

    Sustainability goes beyond green slogans. Our reaction protocols minimize solvent waste and rely on recyclable input streams wherever possible. As more customers conduct life cycle analyses and carbon accounting, the knock-on effects of minimized waste streams, reduced transportation energy, and fewer purification cycles become tangible business advantages. The quiet role of 4-Methoxy-2-Formylphenylboronic Acid in reducing total environmental footprint compared to less selective, higher-waste reagents continues to emerge in client sustainability reports.

    Shaping the Future of Advanced Synthesis

    Every day, teams behind the scenes build the backbone of the chemical supply chain—production planners, plant operators, QC analysts, and technical service experts. Their combined diligence and field feedback give shape to every kilo of 4-Methoxy-2-Formylphenylboronic Acid we produce. We don’t rely on reputation alone. Lab directors tour our facility and see for themselves the protocols that go into every step. Auditors regularly inspect both our process validation records and our deviation logs; corrective action and best-practice sharing loops run continuously.

    With the pace of new molecule development accelerating worldwide, reliable access to well-characterized building blocks becomes more important. In project kickoff meetings, process designers now add more granularity to supply chain risk assessments. Volatile supplies or inconsistent performance of a single reagent can shift schedules by months. That’s why product stewardship means more than just keeping stock on the shelves. Thoughtful manufacturing of intermediates like 4-Methoxy-2-Formylphenylboronic Acid underpins the broader progress of both research and commercial chemistry.

    Collaborative Problem Solving and Continuous Improvement

    The history of our experience with this compound is filled with both learning and practical results. Early in its commercial adoption, scale-up exposed issues with crystallization and filtration that weren’t obvious on lab scale. Learning from pilot failures led our team to change solvent ratios, adjust quench steps, and automate drying. These incremental process improvements, often tested side-by-side against previous methods, contributed to downstream cost savings and more robust handling. We hear from clients that such changes ripple into better overall plant efficiency.

    Process development never stands still. As researchers pursue more complex drug scaffolds and materials, the demands on 4-Methoxy-2-Formylphenylboronic Acid evolve as well. Some projects now require kosher or halogen-free status; others focus on minimizing trace metals below ultra-low detection thresholds. Our QC teams learn and adapt, deploying new test methods and refining procedures with input from both global customers and regulatory partners. It’s the direct feedback loop—report, test, improve, document—that sets our operation apart from mere trading houses or distribution networks.

    Practical Takeaways for Industry and Research

    In the broader view, 4-Methoxy-2-Formylphenylboronic Acid stands as a testament to the impact of small-molecule innovation on big industry challenges. A thoughtfully chosen starting material can simplify routes, cut costs, reduce risk, and advance sustainability—all while raising the quality of downstream products. Its performance, sustainability profile, and adaptability make it a core part of many complex syntheses, especially where quality and reproducibility cannot be compromised.

    Continuous investment—both in plant operations and scientific know-how—ensures that every batch produced meets the bar set by today’s fastest-moving industries. Through rigorous documentation, traceable production, and hands-on technical guidance, we strive to keep our customers equipped for both current and future demands.

    Experience tells us that the best chemistry doesn’t happen by accident. It takes careful design, persistent problem solving, and reliable manufacturing, batch after batch. The continued story of 4-Methoxy-2-Formylphenylboronic Acid in our facility reflects this principle, supporting chemists and engineers as they build the next wave of innovation, one well-made molecule at a time.