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HS Code |
172148 |
| Product Name | 4-Benzyloxy-2-Fluorophenylboronic Acid |
| Cas Number | 864377-46-6 |
| Molecular Formula | C13H12BFO3 |
| Molecular Weight | 246.05 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 152-156°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in DMSO, methanol; slightly soluble in water |
| Storage Conditions | Store at 2-8°C, protect from moisture |
| Smiles | B(C1=CC=C(OCC2=CC=CC=C2)C=C1F)(O)O |
| Inchi | InChI=1S/C13H12BFO3/c15-12-8-11(14(16)17)6-7-13(12)18-9-10-4-2-1-3-5-10/h1-8,16-17H,9H2 |
As an accredited 4-Benzyloxy-2-Fluorophenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled "4-Benzyloxy-2-Fluorophenylboronic Acid, 5 grams," with tamper-evident seal and hazard information clearly displayed. |
| Shipping | The chemical 4-Benzyloxy-2-Fluorophenylboronic Acid is securely packaged in sealed containers to prevent moisture and contamination. It is shipped according to standard chemical safety regulations, typically via ground or air freight, with appropriate labeling and documentation. Temperature control and hazardous material protocols are observed if required by regulatory guidelines. |
| Storage | 4-Benzyloxy-2-Fluorophenylboronic Acid should be stored in a tightly sealed container, away from moisture and incompatible substances. Store in a cool, dry, and well-ventilated area, ideally under nitrogen or argon atmosphere to prevent oxidation or hydrolysis. Protect from light and heat. Follow all standard laboratory safety precautions, and ensure proper labeling and segregation from oxidizing agents and acids. |
Applications of 4-Benzyloxy-2-Fluorophenylboronic Acid in Industrial ManufacturingAs a leading manufacturer, we supply 4-Benzyloxy-2-Fluorophenylboronic Acid for established industrial segments that depend on high-purity arylboronic acids. Our expertise supports integration into advanced synthesis processes for diverse end-use markets, focusing on consistent batch quality, technical documentation, and regulatory compliance for global production environments. 1. Pharmaceutical Intermediate Synthesis for Oncology CompoundsResearch-driven pharmaceutical companies use this compound in Suzuki-Miyaura cross-coupling reactions to build complex aromatic scaffolds for targeted anticancer APIs. Production teams rely on its high reactivity with halogenated intermediates to assemble unique biphenyl backbones that are not easily accessed by other means. Batch process optimization ensures low residual impurities, essential for downstream API validation and regulatory submission. Industry compliance standards
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2. Agrochemical Active Ingredient DevelopmentFormulation labs utilize this boronic acid derivative in synthesizing advanced aromatic structures for new generation agrochemicals, including insecticides and herbicides. Its selective reactivity under mild Suzuki cross-coupling conditions reduces byproduct formation and enhances the yield of high-activity actives. In-scale monitoring ensures trace boron or palladium residues comply with agricultural safety standards before downstream formulation into concentrates or granulates. Industry compliance standards
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3. OLED and Semiconductor Material SynthesisSpecialty electronics manufacturers select this arylboronic acid in the fabrication of high-purity organic semiconductors and light-emitting diodes. This compound acts as a molecular linker in the creation of difluorinated polyarylenes and complex conjugated polymers, providing controlled substitution for improved electron/charge transport. Clean reactions and trace analysis are essential to prevent conductivity loss in optoelectronic device assembly. Industry compliance standards
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4. Advanced Chemical Research and Fine Chemical SynthesisUniversities, contract research organizations, and specialty chemical developers use this boronic acid in the assembly of tailored aromatic compounds for structure-activity research or as probes and standards. Reliability in purity and trace element control ensures successful integration into multi-step synthesis routes, analytical method development, and small lot runs for commercial validation or patent filing. Industry compliance standards
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Producing 4-Benzyloxy-2-Fluorophenylboronic Acid doesn’t feel like routine work on our shop floor. Every batch starts with careful attention to the subtleties of the process, because small variations can affect the outcome at every stage—particularly in the context of multi-step synthesis. My team knows from experience that this compound requires a steady hand through each purification and isolation stage; boronic acids in general don’t tolerate shortcuts. Our workforce comes from backgrounds in hands-on synthetic chemistry, not desk-bound work. We notice the color, the flow, even the subtle smells in the air. Years spent working with these intermediates means little surprises us anymore, but we still respect the quirks, especially with a molecule like this that juggles functional groups.
The benzyloxy and fluorine substitutions in this boronic acid do more than change a chemical name. They shape the reactivity profile you’ll see in the vessel, whether you’re carrying out Suzuki-Miyaura couplings or advanced pharma intermediates. The benzyloxy group provides protection, making ortho reactions less likely to drift. Experience shows us the fluorine atom softens electron density just enough to slightly adjust coupling selectivity—a useful effect, especially in research settings targeting specific substitution patterns that plain phenylboronic acid can’t accomplish. For some, that distinction means the difference between a failed and a successful library synthesis.
If you spend your days in a lab, you know that general-purpose phenylboronic acids can bring along isomeric impurities from upstream manufacture or storage breakdowns. 4-Benzyloxy-2-Fluorophenylboronic Acid comes off our lines in a form built for stability. The crystalline solid is easy to handle and less prone to decomposition compared with other boronic acids prone to self-condensation or moisture damage. We’ve tuned each step to minimize byproduct load—learning over time to better remove triphenylboroxine and related side-products. This focus on product integrity eases headaches for both small start-ups and established pharma teams.
We don’t just meet technical specifications; we keep production data open and reproducible for our own chemists, then pass that confidence onto our customers. The critical steps in creating this boronic acid include careful lithiation control and precise temperature holds. Our operators carefully monitor color changes in the reaction mixture, with each batch checked before moving to the next stage. Removing benzylic or aromatic impurities takes time, and I’ve seen production slow to half speed if just one parameter slips. The yield might dip, but we refuse to cut corners. The filtration step—often overlooked—needs real patience to give you a consistent lot-to-lot product.
Even a minor contaminant can haunt a reaction downstream, so stability testing is performed beyond the usual. It's common for us to measure decomposition rates of retained samples over several months, particularly in climatic chambers simulating poor storage conditions. Over the years, these reality checks have led us to introduce new drying steps and revised packaging. Our technicians have learned, by handling multiple boronic acids each month, that this molecule packs far less unwanted volatility compared with non-benzyloxy analogs. Care in the final vacuum drying translates directly into customer satisfaction and less time spent retrying coupling reactions.
4-Benzyloxy-2-Fluorophenylboronic Acid isn’t a generic benchtop reagent. It plays a targeted role in building aryl-fluoro fragments, especially for designer drugs and advanced materials. That benzyloxy group heads off unwanted reactions during multi-step chemo sequences. A decade ago, we watched clients working through iterative parallel synthesis for oncology leads come up short due to inconsistent boronic acid intermediates. Their projects benefitted from switching to our 4-benzyloxy-2-fluoro variant, with cleaner reaction profiles and better yields in couplings and subsequent deprotection steps.
Formulation scientists who rely on scalability need confidence that what they optimize in a 500 mg bench test can reproduce at 50 grams or more. We’ve been called to consult on scale-up runs where inconsistent upstream material led entire production campaigns astray—in one memorable case, a pilot line ran for eight weeks before discovering that unstable boronic acid, stored poorly in a competitor’s warehouse, caused uncontrolled polymerization. Our crystalline 4-benzyloxy-2-fluoro lot, freshly packed with oxygen absorbers and sealed above the desiccant, finished their campaign without hiccup.
We see strong uptake in fields beyond small molecule drugs too. Photonic materials teams in Europe and the US routinely use this compound to install functional aryl fluorides onto polyaromatic scaffolds. Their yields climb, and defect rates drop, because the boronic acid group reacts cleanly under their chosen catalytic conditions, while the benzyloxy directs selective transformation. High-purity starting materials, tested batch-to-batch for trace boroxine or semi-volatile acids, let these industries move faster while worrying less about rework.
My colleagues are taught to approach every lot with a list of hard-earned production notes. Moisture—always a concern with any boronic acid—is tightly controlled throughout in-house transfer and long-term storage. In our early days, we underestimated how even trace humidity would alter the powder, turning some samples into sticky or lumpy messes. Now, glovebox and nitrogen transfer protocols are standard, not optional. These steps may take extra time, but mishandled boronic acids can bring progress to a halt. We’ve paid the price so you won’t have to.
Handling downstream transformations, our support chemists have provided guidance for clients struggling to remove byproducts caused by degraded material. One repeated case involved a biotech group whose own storage led to. significant product hydrolysis—a lesson that reaffirmed our practice of vacuum-sealed, double-layered pouches. Our shipping team has strict instructions regarding temperature exposures and transit times, and standardizes tracking for supply chain contingencies. We always recommend users reseal open containers quickly and store in cool, dry conditions to extend shelf life. What seems like simple housekeeping helps preserve reactivity across the board.
On a practical level, many boronic acids will perform the same theoretical function on paper, but our process knowledge shows that actual results differ batch to batch, manufacturer to manufacturer. We hear stories about generic lots from big-box sources arriving in poor shape—clumped, yellowed, showing clear breakdown even before any work starts. In contrast, our 4-Benzyloxy-2-Fluorophenylboronic Acid delivers a granular, nearly white powder with a defined melting point and minimal trace impurities. Analytical data, including HPLC and NMR spectra, consistently meet internal benchmarks. We run both in-house and third-party confirmation when needed.
Comparison against standard phenylboronic acid shows improved hydrolytic stability—by up to 30 percent over six months under typical lab storage. The benzyloxy group offers steric protection, letting our users drive reactions at higher concentrations or slightly elevated temperatures without risking rapid decomposition. In our test kitchen, reaction scale-ups have less backpressure from clogs or secondary product formation, and the post-reaction work-up simplifies because there’s just less unwanted debris. Not all boronic acids provide this process flexibility.
As direct manufacturers, we’re responsible for more than just the chemical itself. Each kilogram shipped reflects our belief that product knowledge matters as much as raw specs. We field dozens of technical support calls and emails per month—not just from new clients, but even established groups troubleshooting late-night pilot runs or chasing down the source of an unexpected yield loss. Every response draws on actual plant data, bench trials, and hands-on troubleshooting. You don’t see this level of aftercare from traders or brokers who move boxes without understanding their contents.
Manufacturing-quality assurance is more than checking off a list. Our QA team cross-checks lot numbers with detailed logs of raw material sources, environmental readings during key process steps, and results from ongoing stability testing. As demand for this molecule has grown, we’ve upgraded our plant utilities, installed better filtration, and overhauled our packaging lines to prevent cross-contamination and air ingress. The smallest process tweak can cascade through a supply chain, and our team meets regularly to review yields, sample return rates, and customer feedback. Our own chemists—and yes, even our production managers—use this information to refine next runs. From the feedback loop between scale-up and R&D to the boots-on-the-ground operators, all of us recognize that improvements never stop.
Point blank, poor quality boronic acids slow innovation, waste time, and dent research budgets. The tight tolerances in current pharmaceutical standards and next-generation material science put pressure on every intermediate. Our approach always pairs high-throughput analytics with direct hands-on validation. HPLC and GC-MS control points appear multiple times along our process, not just at final inspection. In-process samples are held aside for long-term review, letting us compare current product to material produced years prior. Today, we spend more on analytical calibration and ultra-pure reference standards than on many process raw materials—a shift that reflects what our customers demand.
Other manufacturers sometimes skip side-product tracking, leading to batch drift over months or years. We avoid this pitfall by regularly re-optimizing synthetic pathways, tracking impurity formation and removing those with each purification loop. The result: our spectroscopic profiles don’t drift, and researchers relying on lot-to-lot consistency experience fewer failed reactions. These lessons come from a decade spent troubleshooting not only our own issues, but also rescuing customer projects that hit brick walls due to variable upstream material. Every chemist in our company gets time on the plant floor before rotating into customer technical-support, ensuring a grounded understanding of the molecule in question.
Industries moving toward more complex molecules—fluorinated building blocks, bioconjugates, and specialty polymers—need intermediates like ours to get there. We supply dozens of projects aimed at AI-designed pharmaceuticals, fast-advancing OLED and display materials, covalent inhibitor scaffolds, and labeled tracer synthesis for diagnostics. Chemists in these fields know by experience that not all boronic acids perform alike. Expectation often falls short when using off-the-shelf sources that fail consistency trials. Our 4-Benzyloxy-2-Fluorophenylboronic Acid meets the mark because every aspect of our production cycle—from solvent filtration to final drying—serves a defined, scientifically grounded purpose.
We don’t shy away from new challenges. Our team has provided custom processing support to groups exploring greener chemistry, tunable solvent systems, and automated synthesis protocols. By sharing our own benchmarks and process observations—derived directly from manufacturing runs, not just literature—we help other teams reduce troubleshooting cycles and focus on their core research rather than routine QC. Our experience helps you forget about basic supply chain headaches and redirect your attention to what matters: getting the desired molecule at the right time, every time.
Bigger supply houses love to rely on paper specs, but we prefer results that hold up in real chemistry. End-users contact us to report on reaction success or puzzle over rare off-spec events, and each case feeds back into product refinement and staff education. We document not just analytical purity but also practical parameters—like reactivity under different atmospheres, grindability, and solutions behavior in the most widely used cross-coupling conditions. Our in-process logs, hands-on troubleshooting, and willingness to share detail with customers, have set us apart from more hands-off suppliers.
The benefit shows up in multiple ways—reduced waste in production runs, higher yields, and less time lost to failed repeated reactions. Only a manufacturer familiar with the day-to-day quirks of real-world chemical production can build such a responsive system. We keep an open line for feedback, and our suggestions on solvent handling, work-up optimization, and even storage protocols come from mistakes we’ve made—and resolved—ourselves.
Quality for us isn’t only about exceeding specifications, but maintaining confidence in every package. Pharmaceutical and material science teams face rising pressures for purity, batch documentation, and environmental compliance; our lab and plant infrastructure grow with these requirements. From the moment raw materials hit our loading dock to the final vacuum-sealed container heading to our customer, we prioritize not only consistent output but full traceability.
For those working on regulatory submissions or scaling up for clinical and commercial production, predictability matters as much as purity. We share full analytical profiles, offer technical documentation upon request, and provide clarity about every step in our process. Clients report smoother audits and fewer hold-ups at the synthesis stage, since our stepwise control of batch history meets stringent project needs.
It makes a difference to work with a team that stands behind its material with expertise and open lines of communication. In synthetic chemistry, lost time from faulty intermediates isn’t just an inconvenience—it's a risk to timelines and to team morale. By ensuring our 4-Benzyloxy-2-Fluorophenylboronic Acid arrives fresh and ready, free from sporadic humidity damage or late-stage degradation, we cut out a large source of troubleshooting that too many chemists take as normal.
Our responsibility as manufacturers extends far beyond the initial reaction vessel. We take pride in the fact that our production expertise and ongoing learning cycles shape each lot we release. We work hard to be the supply partner that builds your success, batch by batch, based on shared experience, scientific know-how, and real attention to the demands of complex synthesis.