|
HS Code |
609966 |
| Product Name | 2-Fluoropyridine-5-boronic acid pinacol ester |
| Chemical Formula | C11H15BFNO2 |
| Molecular Weight | 223.05 g/mol |
| Cas Number | 870299-33-1 |
| Appearance | White to off-white solid |
| Purity | Typically >97% |
| Solubility | Soluble in organic solvents (e.g., DMSO, dichloromethane) |
| Storage Conditions | Store at 2-8°C, protected from moisture and light |
| Smiles | B1C=CC(=NC1F)OC(C)(C)C(C)(C)O |
| Inchi | InChI=1S/C11H15BFNO2/c1-11(2,15-7-4-5-10(14)13-6-7)16-12(3)8-9(13)10(14)8/h4-6,8-9H,1-3H3 |
| Synonyms | 2-Fluoropyridine-5-pinacol boronate |
As an accredited 2-Flouropyridine-5-boronic acid pinacol ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-Fluoropyridine-5-boronic acid pinacol ester is supplied in a 5-gram amber glass vial with airtight, tamper-evident cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-Fluoropyridine-5-boronic acid pinacol ester ensures secure packaging, moisture protection, and safe bulk chemical transport. |
| Shipping | 2-Fluoropyridine-5-boronic acid pinacol ester is shipped in tightly sealed containers suitable for chemicals, with appropriate labeling and documentation. It is transported under ambient conditions unless otherwise specified, ensuring protection from moisture and light, and in compliance with relevant local, national, and international regulations for chemical handling and safety. |
| Storage | 2-Fluoropyridine-5-boronic acid pinacol ester should be stored in a cool, dry, and well-ventilated place, away from moisture and sources of ignition. Keep the container tightly closed and protect from direct sunlight. Store under inert atmosphere, such as nitrogen or argon, to prevent hydrolysis or oxidation. Follow all relevant safety protocols and handle with appropriate personal protective equipment. |
| Shelf Life | 2-Fluoropyridine-5-boronic acid pinacol ester is stable for at least 2 years when stored cool, dry, and under inert atmosphere. |
|
Purity 98%: 2-Flouropyridine-5-boronic acid pinacol ester with purity 98% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures excellent yield and minimal impurities. Molecular Weight 239.98 g/mol: 2-Flouropyridine-5-boronic acid pinacol ester with a molecular weight of 239.98 g/mol is used in organoboron-mediated Suzuki coupling reactions, where accurate molecular weight allows precise stoichiometric calculations and reproducible results. Melting Point 75-80°C: 2-Flouropyridine-5-boronic acid pinacol ester with a melting point of 75-80°C is used in solid-phase synthesis processes, where defined melting behavior facilitates controlled processing and product handling. Particle Size <10 µm: 2-Flouropyridine-5-boronic acid pinacol ester with particle size less than 10 µm is used in fine chemical preparations, where small particle dimension promotes rapid dissolution and homogenous mixing. Stability Temperature up to 40°C: 2-Flouropyridine-5-boronic acid pinacol ester stable up to 40°C is used in automated chemical synthesis platforms, where enhanced thermal stability prevents decomposition under operational conditions. Assay ≥99%: 2-Flouropyridine-5-boronic acid pinacol ester with assay ≥99% is used in high-purity catalyst development, where excellent assay values guarantee reliable reactivity and catalyst performance. Water Content ≤0.5%: 2-Flouropyridine-5-boronic acid pinacol ester with water content ≤0.5% is used in anhydrous organic synthesis, where low water content minimizes hydrolytic side reactions for improved efficiency. Solubility in THF >50 mg/mL: 2-Flouropyridine-5-boronic acid pinacol ester with solubility in THF greater than 50 mg/mL is used in boronic ester-based organic transformations, where high solubility enhances reaction rate and scalability. Chemical Stability up to 6 months: 2-Flouropyridine-5-boronic acid pinacol ester with chemical stability up to 6 months is used in long-term storage applications, where extended shelf-life assures batch-to-batch consistency. |
Competitive 2-Flouropyridine-5-boronic acid pinacol ester prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
On our shop floor, handling specialty chemicals like 2-Fluoropyridine-5-boronic acid pinacol ester keeps us rooted in the everyday reality of research and production. What we put into synthesis matters just as much as what comes out. Over years, watching customers work through the same bottlenecks—low-yield boronates, batch-to-batch unpredictability, unexplained impurities—we recognized the need for hands-on control from raw materials to final purification. So, instead of relying on brokers or contract shops, we bring each step under our own roof, where tweaks can be made in real-time. That is how we've lowered the variability associated with this class of boronic pinacol esters and earned the confidence of end users who depend on reproducible quality.
In our industry, directly controlling production parameters makes a bigger difference than most realize. We see the impact not in words, but in chromatography reports, in NMR spectra where side peaks fade, and in the number of times we don't get calls about reaction stalls. Some chemical products, including 2-Fluoropyridine-5-boronic acid pinacol ester, are more sensitive to trace moisture or metal ions than standard libraries suggest. Many outside manufacturers cut corners in drying, choosing easy filtration over careful solvent control, or ignoring packaging flaws that introduce spoilage on the shelf. We've had to figure out the hard way what works—swapping glass lines for Teflon where it matters, oxygen-scavenging at the pinacol coupling step, and choosing shipment containers that don't just look good on a data sheet but actually prevent slow hydrolysis during long transit.
For synthetic chemists, every step forward in handling intermediates reduces lost hours and wasted material. We realized early that reliable supply of this ester builds confidence among formulation scientists, who cannot start screening a batch of analogs only to discover microgram differences in assay or contamination. Our own technicians know the demands of tight timelines, and they've fed that experience into tightening our protocols for both preparation and shipment. We learned firsthand from customers in pharma and material science how delays ripple through whole research campaigns. As a result, our in-house synthesis blends high-throughput with attention to those nitty-gritty details—so product arrives exactly as described, every time.
From the first runs of this compound, we recognized that the consistency of melting point, purity, and moisture content has more impact than technical bullet points can show. Our batches of 2-Fluoropyridine-5-boronic acid pinacol ester typically meet or exceed 98% by HPLC, supported by proton and fluorine NMR to confirm substitution pattern and absence of pinacol impurities. At scale, pinacol esters like this one offer a measurable advantage in Suzuki-Miyaura cross coupling. During process validation with partners, we have seen the value of reduced protodeboronation under typical coupling conditions; the enhanced solubility in a variety of organic solvents translates into higher conversion even without excessive ligand loading.
Synthetic applications in medicinal chemistry push the boundaries with every new target. Our own teams have stress-tested this compound in palladium- and nickel-catalyzed couplings, targeting both aryl and heterocyclic electrophiles. Real world experiments reveal where theoretical yield starts getting eaten up by unknown byproducts, or where a catalyst stalls due to residual water. That's why, in our operations, we've adopted in-line moisture analysis and post-purification dryness checks. Powder XRD and DSC measurements support stability data, which translates into a longer shelf-life than many reported alternatives.
Most users arrive at our landing page looking for a reliable starting point in heterocycle synthesis. Pyrazoles, pyridine derivatives, and non-benzenoid aromatics with fluoro and boron functionality remain tricky from both a reactivity and handling standpoint. We've steered clear of mass-market assumptions, focusing instead on what actually happens in the flask. This means producing the material as a pale, free-flowing solid—free of sticky agglomerations, which are early warning signs of pinacol ester degradation or water uptake. In our own hands, reactions performed with this material do not show the unexplained lag phases that hit productivity in high-throughput screening.
We do not chase the lowest-cost route. Alternative processes may deliver nominal product, but we've traced issues back to minor batch contaminants—like unreacted pinacol, or mixed boronic esters that interfere during late-stage couplings. From our analytic runs, we notice subtle differences in the color and odor of product lots, correlating odd notes to higher levels of organoboron side products, peroxides, or even organometallic residues. Open communication with our QC team makes it easy to flag batches that need rework, rather than passing them down the line under generic specs.
Looking at the broader boronate ester landscape, chemists face real tradeoffs. The classic boronic acids hydrolyze readily, producing problematic boric acid or forming oligomers that gum up reaction setups. We used to see frustration in the lab when users had to dry boronic acids before each reaction, wasting valuable time. Over a dozen lab trials, our own teams confirmed pinacol esters hold up better to ambient conditions and can be weighed and transferred without fuss. For 2-Fluoropyridine-5-boronic acid, the pinacol ester brings a key advantage—lower susceptibility to moisture means longer bench stability, even as the free acid reacts more quickly in the coupling flask.
One difference that stands out to experienced hands: boronic pinacol esters like ours often dissolve smoothly in typical Suzuki reaction solvents, including toluene, THF, and even DMF. This lowers the activation barrier for scale-up, making the transition from milligram screening to gram or kilogram demonstration runs more predictable. Unlike some alternatives, we don't see precipitation during the setup phase which would otherwise affect reproducibility or force repeated filtration steps.
By paying attention to the real-world pain points—clumping, variable purity, trace metal contamination—we've shown that a steady, reproducible ester can actually raise productivity across screening platforms. Many commercial suppliers stretch overheads to deliver a one-size-fits-all grade, but on-site synthesis allows us to tailor the clean up for optimal performance—not just nominal purity, but also elemental profiles and trace solvent content. Our product consistently meets or beats internal limits for iron, copper, and other catalyst poisons, drawing on both freshly purified inputs and regular cleaning of reactor surfaces. These incremental improvements pay off in smooth, high-yield couplings.
When alternative boronate esters or other protecting groups have been compared in practice, reaction workflow often tells the real story: ease of handling, lower hazard risk, and decreased need for error checking. We still recall the time a research team shared their surprise at finishing a coupling run a day ahead, just because the starting material handled as a dry solid rather than a sticky or oiling liquid. Such moments reveal the true value of attention to process over simply ticking the usual purity box. Our QA team often shares these stories internally, reinforcing what consistent product can enable further down the line.
Even though 2-Fluoropyridine-5-boronic acid pinacol ester may look like just another white powder, its reliability impacts whole development timelines—from medicinal chemistry screens up to process engineering. Whenever our larger clients move from discovery to kilogram synthesis, they need to be sure each new order matches their pilot run. Unlike resellers who only pass along certificate of analysis PDFs, we perform project-by-project reviews. In troubleshooting scale-ups, we've caught subtle differences in exotherm behavior when starting material from different sources is switched in. Customers value that we can provide batch history and customization for solvent residue or specific packaging requirements—directly from our records.
Investing in scale isn’t about just running bigger pots; it asks for more robust filtration, more reliable drying, and flexible containment for air- or moisture-sensitive intermediates. Our staff spends as much time on packaging as on reaction chemistry, using real feedback from users. For larger orders, we've transitioned away from generic zip bags or foil packets, instead working with packaging engineered to block gradual air or moisture exposure. This kept one key client on track during a summer shipping mishap, teaching us firsthand that smart handling doesn't just improve lab-scale synthesis but also prevents massive batch failures at plant scale.
Every chemical process we develop for ourselves produces new data. Sometimes, minor process impurities reveal mechanisms that wouldn’t show up in limited academic runs, guiding us to cleaner reactions and ultimately cleaner product. Lab teams outside our walls value that every lot matches what is promised, because we back up every shipment with targeted analytics—not just simple purity testing, but full impurity profiling and moisture content down to parts-per-thousand. We believe talking directly about these details helps customers plan their own analytic runs, rather than piecing together info from disconnected distributors.
Regular communication with process engineers keeps us adapting to new requirements. Recent debates around the use of different catalyst systems highlighted how subtle differences in boronate ester quality can swing whole process outcomes. For industrial users, even slightly elevated iron or copper causes otherwise robust catalysts to lose activity. By taking direct ownership over both synthesis and purification, we can guarantee that our finished 2-Fluoropyridine-5-boronic acid pinacol ester stands apart from generic mass-market samples that often leave researchers guessing.
Chemists encounter new coupling challenges every year—each drug analog or material prototype demands tweaks that no catalog entry can anticipate. In our own research work, we’ve put this compound through chemoselective couplings, trying out various palladium systems and base/ligand combinations. Some teams need robust compatibility with electron-deficient partners, others test borylation selectivity. In both arenas, we have seen how trace water or particulate impurities typical from third-party batches can kill yield at scale. By running these reactions in-house, we reveal small differences—sometimes, it has taken multiple runs and interlaboratory checks to really validate quality improvements.
Real-life feedback shapes how we iterate. A material scientist working on novel OLED materials needed reliable boronate esters that didn’t darken during scale-up. Small changes in residual metal levels caused knock-on issues in their thin film properties. By switching to our in-house material—tested for trace elements beyond required minimums—they produced stable films across batches. It’s a clear reminder that chasing theoretical purity isn’t enough: the full impurity profile and robustness under real lab conditions keep the end use reliable.
Medicinal chemists often need to prepare a range of analogs in short order. The difference between a high-purity, stable starting material and a variable, problematic one can amount to weeks of scientist effort. We’ve heard stories where a promising reaction path got put on hold due to a single shipment of off-grade raw material. After swapping to a batch with low moisture and no visible degradation, the project resumed within days. These are the sorts of insights we build into our process: not just batch checks, but feedback loops allowing improvement with every kilogram shipped.
Producing 2-Fluoropyridine-5-boronic acid pinacol ester for varied users has taught us to expect the unexpected. Even subtle differences in temperature and pressure during synthesis shift reaction profiles. Our reactors use both real-time monitoring and controlled ramping to shave down impurity formation. Testing at each stage helps root out issues before the final crystallization. Early on, we found that a single leaky gasket or a poorly rinsed filter press can introduce off-odors, color, or trace metals—clues that something needs reengineering. These observations led us to review every point of contact and to overhaul filtration and oxidation steps with the goal of delivering consistently pure product for each customer order.
Supply chain headaches affect everyone in chemicals, especially for reagents dependent on specialty boronic acids or tricky halogenations. Surging demand or shipping holdups make some manufacturers cut corners, producing uneven or questionable batches. We made a decision to keep control over sourcing, raw material storage, and batch tracking, making the occasional tough call to pause or slow production rather than compromise quality. Those experiences shaped our belief that long-term reliability and transparency matter even more than headline production numbers.
Environmental responsibility factors into each batch as well. Rather than dumping wash solvents or skipping quality control to save a day, our process integrates solvent recovery and purification with regular environmental audits. While this raises our direct costs, in the long run it preserves both lab safety and our reputation with clients who demand real stewardship. This kind of operational transparency goes beyond a QA paragraph; it keeps our site running, and our customers on track for their own regulatory compliance.
Our investment in this compound stems from seeing the role it plays in modern chemistry—enabling transformations that would be prohibitive or unreliable with older reagents. As manufacturing chemists, our perspective differs from brokers or trading houses: we witness the results of smart process control, honest feedback, and willingness to rework batches until they match the actual needs expressed by researchers. Over time, product families such as these form a backbone for pioneering projects—from pharmaceuticals to novel materials—driven by the steady supply of a clean, robust intermediate.
Trust builds over batches, not with headlines. Our product’s difference shows where it matters: in lower downtime, fewer repeated experiments, and a smoother handoff from bench to pilot scale. Lab scientists spend less time fussing over variability, while process teams avoid troubleshooting sessions that drain resources. The gains from our field-driven approach support faster timelines and better science at every stage.
Demand for next-generation molecules won’t slow down. Meeting that need asks for synthesis partners who don’t just fill orders but own the technical outcome. We are proud that our direct production of 2-Fluoropyridine-5-boronic acid pinacol ester offers not only a reagent, but a trusted link in our customers’ progress. Through experience, continual investment, and open dialogue, we help ensure that each project—whatever the end molecule—starts with the right foundation.