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HS Code |
889329 |
| Productname | 3-Fluoro-4-Methoxycarbonylphenylboronic Acid |
| Casnumber | 864070-97-9 |
| Molecularformula | C8H8BFO4 |
| Molecularweight | 197.96 |
| Appearance | White to off-white solid |
| Meltingpoint | 148-152°C |
| Purity | ≥98% |
| Solubility | Soluble in DMSO, methanol |
| Synonyms | 3-Fluoro-4-(methoxycarbonyl)phenylboronic acid |
| Smiles | B(C1=CC(=C(C=C1)F)C(=O)OC)(O)O |
| Inchi | InChI=1S/C8H8BFO4/c1-14-8(11)5-2-3-7(10)6(4-5)9(12)13/h2-4,12-13H,1H3 |
| Storagetemperature | 2-8°C |
As an accredited 3-Fluoro-4-Methoxycarbonylphenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass vial containing 5 grams of 3-Fluoro-4-Methoxycarbonylphenylboronic Acid, securely sealed and labeled with product details. |
| Shipping | The chemical `3-Fluoro-4-Methoxycarbonylphenylboronic Acid` is shipped in tightly sealed containers, protected from moisture and light. Packaging complies with safety regulations for sensitive organic compounds. Shipping typically utilizes temperature-controlled environments to maintain stability and prevent degradation during transit, ensuring safe arrival for research or industrial use. |
| Storage | 3-Fluoro-4-Methoxycarbonylphenylboronic Acid should be stored in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers. Refrigeration (2–8°C) is recommended to maintain stability. Avoid prolonged exposure to air and humidity, as the compound is sensitive to hydrolysis. Use appropriate personal protective equipment when handling. |
Applications of 3-Fluoro-4-Methoxycarbonylphenylboronic Acid in Industrial Manufacturing3-Fluoro-4-Methoxycarbonylphenylboronic Acid is a critical intermediate in multiple fine chemical and pharmaceutical processes. Our production process maintains precise control of purity and traceability to meet demanding application specifications in regulated downstream industries. Below, we present the principal industrial uses, technical details, and relevant regulatory frameworks for this material. 1. Pharmaceutical API Synthesis – Small Molecule DrugsMajor pharmaceutical manufacturers rely on this compound as a boronic acid building block for Suzuki–Miyaura couplings during small molecule API development. It is used in the synthesis of targeted kinase inhibitors, oncology candidates, and CNS drug scaffolds. Downstream customers integrate the material during multi-step processes, combining it with halogenated heterocycles under palladium catalysis to access advanced intermediates with fluorinated, methoxycarbonylated aryl motifs. Stringent control over impurity profiles, residual metals, and particle size supports batch traceability for regulated drug filings. Our facility works with GMP-aligned documentation to assist customers’ DMF and ANDA submissions in multiple regions. Industry compliance standards
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2. Agrochemical Intermediate Production – Modern HerbicidesIn the agrochemical sector, this boronic acid finds frequent application as a coupling partner in the synthesis of modern herbicidal actives containing arylfluorinated motifs. Customers scale-up our product in multi-ton volumes, incorporating it via cross-coupling into ring systems for new-generation, selective herbicides. Each batch is monitored for trace contaminants, as residual boronic esters and solvents may impact downstream environmental registration. Our material provides consistency for multinational agrochemical producers preparing EU REACH dossiers, as well as for final formulation exported globally. Industry compliance standards
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3. OLED and Organic Electronics Material ManufacturingProducers of advanced organic electronic materials choose this building block to construct aryl-boronic frameworks required for high-performance OLED emitters and charge-transport layers. The product enables precise incorporation of both fluorine and methoxycarbonyl groups essential for fine-tuning film morphology and electron mobility within display panels and lighting devices. All lots comply with tight trace metal content and residual solvent specifications to avoid impact on electronic properties and product stability during vacuum deposition or spin-coating processes. Industry compliance standards
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4. Specialty Fine Chemical Synthesis – Fluorinated Building BlocksProducers of specialty fine chemicals employ this boronic acid for introducing unique fluorinated, carboxylated aryl groups into advanced chemical entities. Synthetic chemists integrate it in controlled environments with precisely timed addition to ensure high para-selectivity and consistent product distribution across complex molecular libraries. Each production lot is certified to customer-specific analytical parameters for impurities, water content, and organic residue, supporting critical research as well as commercial launch scale. Industry compliance standards
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5. Active Ingredient Synthesis – Veterinary PharmaceuticalsVeterinary pharmaceutical manufacturers utilize this compound as a key fragment in the synthesis of active ingredients for animal health products, particularly where functionalized aromatic units enhance target binding or metabolic stability. The process typically involves palladium-catalyzed coupling, requiring high-purity raw material to avoid introducing residual boronic acids, which can affect animal safety profiles. Our production maintains full batch traceability, and the supply chain supports VICH-compliant manufacturing and export documentation for state registration dossiers. Industry compliance standards
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Working in chemical manufacturing day in and day out, few molecules catch attention like 3-Fluoro-4-Methoxycarbonylphenylboronic Acid. Every batch we produce reflects not just the culmination of raw ingredients and controlled reactions, but also a commitment to reliability. This compound, commonly referenced by its model number or CAS (for specialists tracking purity and documentation), serves a distinct range of pharmaceutical and material science uses. Because of its molecular design, it offers something unique that routine boronic acids and substituted phenyl derivatives cannot.
Chemists talk about “building blocks,” but on the factory floor, these aren’t abstract ideas—they’re bags of carefully weighed powder, storage drums, glass reactors, and dry rooms smelling of solvent and ozone. 3-Fluoro-4-Methoxycarbonylphenylboronic Acid arrived on the scene as research teams needed boronic acids that could do more in Suzuki-Miyaura cross-coupling, agrochemical synthesis, and medicinal chemistry discovery. The combination of a boronic acid group with fluorine at the 3-position and a methoxycarbonyl group at the 4-position dramatically changes the way the molecule performs in downstream chemistry.
Fluorine atoms matter a great deal. In the rings of hydrocarbons we work with, fluorine stabilizes certain intermediates and bumps up metabolic stability in pharmaceutical candidates. Stirring in a methoxycarbonyl group brings another set of reactivity changes and functional handles. Compared with everyday phenylboronic acid, this compound walks a tightrope between reactivity and selectivity. What ends up in the flask is more than a subtle tweak, it shifts the balance in palladium-catalyzed reactions—something proven time and again both in our pilot batches and in literature examples.
Hand on heart, we focus on traceability directly back to our raw ingredient suppliers. Using consistent, high-purity fluorinated aromatics and alkylating agents brings tighter control to each batch. When drawing samples for NMR and HPLC, the aim stays simple: ensure the product matches stringent pharmaceutical standards, keeping carbon, proton, and boron chemical shifts within target ranges. That’s not just for the paperwork; it means researchers and manufacturers downstream run into fewer surprises during method development or scale-up.
Over the years, our quality assurance teams learned how subtle impurities affect coupling yields. Having produced thousands of kilograms over several campaigns, each consisting of tightly monitored synthesis, isolation, and chromatography, we long ago stopped outsourcing analytics for standard boronic acids. Our team recognized early that reproducibility wins trust with global partners, and that starts at the reactor, not the shipping dock.
Safety draws just as much attention. Every part of the process, from solid transfer to drying, is designed to minimize exposure and contain fine dust, given the reactivity of boronic species. Cleanroom protocols, lab coats, eye protection, and air monitoring stay in place no matter the time pressure. Many in our area forget the risks of poorly ventilated transfer rooms until an incident demands retraining—years of near-misses turned our manufacturing workflow into a blueprint for other sites. Quality and safety meet in how we ground our operations.
Bouncing between requests from academic groups, pharmaceutical companies, and material scientists, we have direct feedback on why this compound stands out. Teams running Suzuki coupling reactions crave boronic acids that hold up during multi-step syntheses. Where phenylboronic acids lose out to competing hydrolysis or protodeboronation, the addition of fluorine can help stabilize intermediates. The methoxycarbonyl group expands reaction possibilities—allowing for further transformations, amidation, or use as a protected acid for later deprotection.
In real-world synthesis, those who’ve tried to build fluorinated biaryl scaffolds for kinase inhibitors recognize the headache that poorly designed boronic acids cause. Some customers need large lots with minimal residual solvent, while others prioritize fine powders for high solubility in polar solvents. We’ve watched as this molecule’s solubility profile opened doors for improved reaction kinetics—saving hours in laboratory development and smoothing the route from microgram bench trials to multi-kilogram production runs.
For companies exploring the interface of medicinal chemistry and process development, a compound like 3-Fluoro-4-Methoxycarbonylphenylboronic Acid can drive projects forward with remarkable reliability. Internal studies among process chemists reveal that reactions using this molecule often enjoy higher isolated yields and cleaner product profiles. Many report less decomposition under standard Suzuki conditions, which means they can reduce waste, save on catalyst, and avoid laborious chromatographic separations.
On the practical side, the question always comes back to: Why not just use a straightforward phenylboronic acid? The answer comes through experience. Standard phenylboronic acids display wide open doors for functionalization but stumble in scenarios where electron-withdrawing or electron-donating effects are needed to target particular rings or coupling partners. Mono-fluorinated boronic acids bring new electrophilic or nucleophilic balances but frequently miss the mark on solubility or reactivity for some applications.
Switching to dual functionalization—here, with both fluorine and methoxycarbonyl groups—transforms the reactivity profile entirely. In our hands, and in the hands of partner chemists, this combination sidesteps several bottlenecks. There’s more selectivity for para-coupling partners. There’s more resistance to side-product formation. As a building block, it opens new possibilities in structure-activity relationship (SAR) explorations—a feature highlighted by numerous lead optimization projects over the past decade.
It pays to talk about scale-up, too. In the realm of kilogram or tonne production, many boronic acid derivatives falter. Low-melting solids, hygroscopic powders, or unstable intermediates make for long hours in the plant. Through numerous campaigns, this compound’s crystalline nature and shelf stability shine through. Our team has loaded pallets for shipment across continents without a single batch recall. Chemical production isn’t glamorous, but reliability keeps production lines moving and meets regulatory scrutiny with ease.
Behind every high-purity drum leaving the loading dock stands a team experienced in scaling tricky fluorinated compounds. We’ve seen what happens when lots come back nonconforming. Reactive impurities—not always visible on first pass analytics—have cost customers valuable time. For 3-Fluoro-4-Methoxycarbonylphenylboronic Acid, we commit to tighter controls over solvent content, water pick-up, and residual byproducts. Real people count on that consistency—not just in pharma, but in materials and specialty applications where impurities can cripple product launch cycles.
Time on the floor has taught us that communication with downstream users tightens up supply chains. Users want certainty, not just a lot number on a barrel. This is why we regularly run sample lots through in-house application trials—testing Suzuki and other cross-coupling conditions, benchmarking against competing materials, and sharing real data with partners looking to qualify new suppliers. No one here wants a customer to be first to discover a hard-to-separate side product or a shipping issue with a heat-sensitive batch. We prefer to catch it at source.
Every industry has its own buzzwords, but for those working in pharmaceutical research, agrochemical design, and advanced materials, the impactful story comes down to what these molecules let you build. For pharma, the 3-fluoro and methoxycarbonyl motifs end up in advanced intermediates for kinase inhibitors and CNS drugs. Structure-activity relationships depend on minute tweaks—inserting fluorine not only tunes binding affinities but also controls metabolic fate in animal models. The methoxycarbonyl group brings strategic flexibility, acting as a protected carboxylic acid, only uncovered when downstream chemistry demands.
Agrochemical developers, especially those chasing patent space for new crop protection products, value unique substitution patterns. The fatty, bulky structure of this boronic acid derivative creates scaffolds resistant to rapid biological degradation. Our own studies in catalysis and field trials have shown improved yield of coupling products, supporting teams racing against the clock during growing seasons.
Material scientists ask about electronic properties—the addition of fluorine tunes electron density, while the methoxycarbonyl group opens the door for future polymerization. Several companies have confirmed improved durability in test coatings and films produced via advanced Suzuki coupling routes. We get occasional requests to further functionalize this structure, a testament to its versatility once it arrives in a well-sealed container from our plant.
Manufacturing compounds with boronic acid groups demands vigilance around hydrolysis and oxidation. Early runs taught us that boronic acids—especially those bearing sensitive functional groups—can foul up product purity if handled carelessly. Labware cleanliness, precise pH control, and gentle drying protocols aren’t just checklist items—they have big impacts on the final material. Years of audits and partner feedback revealed that skipping corners on these steps comes back to bite, sometimes weeks after shipping.
Our site constantly reviews workflow data, capturing deviations and process tweaks. We stumbled, at times, over issues like batch-to-batch color variation or caking in storage drums, each one a reminder of the small margins separating laboratory theory from industrial reality. Revising procedures and collaborating with end users helped build real improvements. Switching from chlorinated solvents to greener alternatives cut down on toxic waste streams, a change supported by both our operations team and downstream partners searching for more sustainable supply chains.
Protecting product quality during shipment became another critical lesson. This compound doesn’t always travel well in humid climates. Modified packaging with multilayer barriers and desiccant packs now ship as the standard after a few early complaints about caked solids. Every change—proposed after feedback, tested through multiple weather cycles, then implemented site-wide—reflects the pragmatism that keeps us in the running as a long-term supplier.
Mistakes in chemical manufacturing have human costs. A poorly filtered batch one year resulted in costly rework, mishandled stock, and a lost customer. Not long after, our team established double-filtration as part of standard operations. Periodic panic over missed deadlines, coupled with the real risk of regulatory review, underpins our insistence on batch sampling and independent cross-checking among shift workers.
Over time, real improvements develop as more than just SOP updates or team retraining. We devote energy to employee up-skilling, cross-department communication, and rapid response. Site safety for handling boronic acids improved after study groups weighed in on solvent vapor control. Partnering with solvent recovery services cut overall operating costs, passing direct and indirect savings to our buyers who demand both sustainability and affordability.
Receiving site visit requests is taken as a responsibility, not a formality. We tour customers through every step—from loading dock to lab bench—to show where their material originates. Years of manufacturing operations have solidified our belief in transparency, which shines brightest on plant tours. Our plant has nothing to hide. Open communication about yield fluctuations or raw material challenges builds long-term deals, not spot buys.
This boronic acid isn’t just another stock item buried in a catalog. For many on our staff, seeing it serve as a backbone for drug candidates or new electronic materials brings pride. Each successful shipment marks months of hard work, from the initial purchase order to the QA sign-off. The value comes through not just in measured purity or paperwork, but also in the positive impact for customers who trust their projects to us.
We are a chemical manufacturer operating amid a network of engineers, operators, QC analysts, and regulatory experts. Our collective experience shapes every batch. Customers—including both high-profile pharmaceutical firms and smaller research upstarts—demand more than just technical specs. They expect insights, frankness about supply risks, and practical partnership in moving their products from idea to market.
3-Fluoro-4-Methoxycarbonylphenylboronic Acid represents the blend of experience and adaptability that fuels our business. Every feedback loop—good or bad—funnels into manufacturing improvements. Partnership grows both when things go right and when we correct our course. Our identity as chemical makers reflects this in every kilo packed and shipped.
No one knows exactly what the next generation of pharmaceuticals or new-tech materials will demand. What stays clear is that increasingly complex molecules drive innovation across every sector. Building blocks equipped with unique reactivity, like this compound, empower researchers to accelerate timelines and explore entirely new chemical space. Our plant invests regularly in scale-up capacity and greener, more robust processes so we can match ambitions on the cutting edge.
We’re invested—personally and professionally—in the success of everyone who uses our products. Each filled drum restates a promise: to meet needs, deliver on time, and provide honesty about what works and what needs improvement. Success, in this line of work, lies in attention to detail and a culture of learning. This molecule, 3-Fluoro-4-Methoxycarbonylphenylboronic Acid, is as much a story about craftsmanship as it is about chemistry. Through each challenge, it proves the value of collaboration between manufacturer and innovator, from process design to final application.