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HS Code |
476081 |
| Product Name | 2-Fluoropyridine-5-boronic acid pinacol ester |
| Cas Number | 112934-03-9 |
| Molecular Formula | C11H15BFNO2 |
| Molecular Weight | 223.05 |
| Appearance | White to off-white solid |
| Purity | Typically >95% |
| Melting Point | 80-84°C |
| Solubility | Soluble in organic solvents (e.g., DMSO, THF) |
| Storage Conditions | Store at 2-8°C, protected from moisture |
| Smiles | B1(OC(C)(C)C(C)(C)O1)c2cnc(F)cc2 |
| Synonyms | Pinacol 2-fluoropyridine-5-boronic ester |
| Cat No | varies by supplier |
| Inchi Key | XWHLCQOYKBSTIQ-UHFFFAOYSA-N |
As an accredited 2-FLUOROPYRIDINE-5-BORONIC ACID PINACOL ESTER factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass vial containing 1 gram of 2-Fluoropyridine-5-boronic acid pinacol ester, sealed with a screw cap and label. |
| Container Loading (20′ FCL) | 20′ FCL loads 2-FLUOROPYRIDINE-5-BORONIC ACID PINACOL ESTER securely in sealed drums, compliant with IMDG regulations, ensuring safe transport. |
| Shipping | 2-Fluoropyridine-5-boronic acid pinacol ester is shipped in tightly sealed, chemically resistant containers under ambient conditions. It should be protected from moisture and direct sunlight during transit. Standard shipping for non-hazardous laboratory chemicals applies, but check local and international regulations for any specific handling or documentation requirements. |
| Storage | Store 2-Fluoropyridine-5-boronic acid pinacol ester in a tightly sealed container under an inert atmosphere, such as nitrogen or argon. Keep it in a cool, dry place, away from moisture, heat, and direct sunlight. Avoid exposure to air and incompatible substances like strong oxidizing agents. Refrigeration (2–8°C) is recommended for optimal stability. Handle under proper laboratory safety protocols. |
| Shelf Life | 2-Fluoropyridine-5-boronic acid pinacol ester is typically stable for two years when stored properly in a cool, dry place. |
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Purity 98%: 2-FLUOROPYRIDINE-5-BORONIC ACID PINACOL ESTER with a purity of 98% is used in Suzuki-Miyaura cross-coupling reactions, where it delivers high yield and selectivity in heteroaryl synthesis. Molecular Weight 249.96 g/mol: 2-FLUOROPYRIDINE-5-BORONIC ACID PINACOL ESTER with a molecular weight of 249.96 g/mol is used in pharmaceutical intermediate production, where it ensures consistent stoichiometry and process reliability. Melting Point 65–68°C: 2-FLUOROPYRIDINE-5-BORONIC ACID PINACOL ESTER with a melting point of 65–68°C is used in automated solid-phase synthesis, where it offers reliable phase transition control and efficient processing. Particle Size < 75 μm: 2-FLUOROPYRIDINE-5-BORONIC ACID PINACOL ESTER with particle size less than 75 μm is used in fine chemical manufacturing, where it promotes rapid dissolution and homogeneous reaction mixtures. Stability Temperature up to 40°C: 2-FLUOROPYRIDINE-5-BORONIC ACID PINACOL ESTER stable up to 40°C is used in material storage and handling, where it preserves chemical integrity and minimizes decomposition risk. NMR Purity ≥ 98%: 2-FLUOROPYRIDINE-5-BORONIC ACID PINACOL ESTER with NMR purity ≥ 98% is used in analytical research applications, where it supports accurate characterization and reliable experimental results. |
Competitive 2-FLUOROPYRIDINE-5-BORONIC ACID PINACOL ESTER prices that fit your budget—flexible terms and customized quotes for every order.
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From our production floor to your research bench, 2-Fluoropyridine-5-boronic acid pinacol ester, catalogued here as Model No: 1635790-17-4, reveals what precise chemistry can achieve. As manufacturers with hands-on responsibility for every batch, we’ve learned that subtle modifications like a fluorine atom and boronic ester functionality turn a relatively simple pyridine ring into a powerful synthon. This compound’s structure offers a gateway to advanced coupling and diversification, especially in the hands of innovative chemists exploring heteroaromatic frameworks.
Our technical teams handle this molecule directly from raw material selection to the last QC step. We see, day after day, the sensitivity that boronic esters can show. Stable pinacol protection prevents rapid hydrolysis, allowing this compound to endure handling on the bench and storage on the shelf. Pinacol’s presence shields the boron center, reducing unwanted side reactions and improving yields during cross-coupling steps. Our experience suggests that, compared to boronic acids, the pinacol ester travels further and survives longer under routine research and pilot plant conditions. This practical value matters in labs scaling from milligrams to kilograms.
The distinct asset of 2-fluoropyridine at position-5 fused to a boronic ester reflects in its reactivity. Not all boronic esters are created equal. Fluorine’s electron-withdrawing nature can tune reactivity in Suzuki-Miyaura couplings, influencing both rate and selectivity. We’ve processed feedback from pharmaceutical and agrochemical clients, confirming that this precise combination opens up pyridyl-fluorinated targets unattainable through simpler boron compounds or non-fluorinated analogs. Change a single atom, lose a world of chemistry: this has been our observation during years of iterative process improvements and partnerships with end-users.
As a manufacturer, reliability never comes from luck. Each production run brings fresh lessons about maintaining consistent purity and minimizing undesirable isomers. The difference between a usable building block and an unpredictable impurity profile often traces back to careful temperature control and solvent management—a daily focus for us, not a talking point. We act on analytical results immediately, not weeks later. Feedback loops between our lab staff and production improvements shape the product on offer: it’s not enough to state a purity; we test for relevant trace byproducts that could derail sensitive catalytic steps. The suppliers’ hands define the success of your synthesis long before the bottle lands in your storeroom.
Chemists reach for 2-fluoropyridine-5-boronic acid pinacol ester when conventional solutions fall short. Demand for pyridine derivatives stretches across pharmaceuticals, crop protection, advanced materials, and ligand design. Each of these fields depends on subtle fine-tuning of molecular structure. We’ve witnessed firsthand how this ester supports efficient C–C bond formation, helping researchers push past simple substitutions and into complex architectures. Cross-coupling, especially under Suzuki conditions, dominates its use. We’ve supported projects that needed to bypass problematic halides and move straight into boronate-couplings to access scaffolds that define today’s medicinal chemistry.
Having run processes for both boronic acids and alternative esters, real differences emerge. Boronic acids, as direct analogs, tend to degrade or polymerize, raising storage and transport headaches. Pinacol esters deliver stability and ease of weighing, making scale-up feasible without specialized equipment. Non-fluorinated pyridines might seem interchangeable, but the distinctive electronic effects of fluorine frequently mean higher selectivity and resistance to metabolic oxidation—features valued by both drug developers and material scientists. We collaborate closely with formulators who require the right balance of stability, reactivity, and functional-group tolerance. Years of direct feedback show that 2-fluoropyridine-5-boronic acid pinacol ester repeatedly meets these challenges.
We tackle obstacles no reseller ever faces. Batch scaling raises questions about exothermicity, phase solubility, and solid-state behavior of intermediates. We track what happens as reaction volumes move by orders of magnitude, and make adjustments at the level of mixing, base addition rates, and drying methodology. By working bottom-up, our team fine-tunes crystallization and filtration so the product maintains quality from gram to tonne. The truth is, overlooked technical details become client problems if the manufacturer isn’t continually optimizing. We’ve invested in analytics tailored to 2-fluoropyridine boronates—NMR routines that catch minute pinacol byproducts and ensure tight specification controls.
A compound that stumbles out of the starting gate burdens the whole supply chain. As manufacturers, our reach stops at the bottle, but our reputation travels on as chemists in the field realize fast whether they’ve received a clean, workable building block. We’ve responded to line stoppages where an unexpected impurity cost weeks of research and strained collaborations. Working directly with project chemists helps us spot trends in what they wish worked better, and we channel these hopes into both process tweaks and education for our own staff. The best products are the result of conversations, real lessons, and hands-on trials.
Every batch holds the possibility of deviation. Color, melting point, and chromatographic purity show the visible side of chemical control. Less obvious are trace metals or pinacolate residues. Downstream applications—especially in API research—demand tight limits. We keep logs on solvent lots, reagent batches, and environmental exposure for each production run. This traceability isn’t about paperwork; it shortens troubleshooting, saves time, and reassures every chemist that more than a label backs that flask. Over years, these logs have helped us track issues, spot patterns, and make proactive improvements.
True manufacturing involves more than molecule-making. Solvent recovery, waste neutralization, and emissions controls form part of our everyday work. Byproducts from boronic ester synthesis sometimes create headaches if left unmanaged. We adapt processes as regulations evolve and stay in front of stricter controls. Our team regularly pilots new waste minimization ideas, from solvent swaps to on-site recovery, reducing impact without sacrificing quality. We share results and lessons on these efforts with industry partners, pushing the whole field forward.
The world of advanced synthesis rarely accepts off-the-shelf answers. Our customers often devise routes that force our product to perform under exacting conditions. Microwave reactors, continuous flow setups, or unconventional solvents can stress-test even the sturdiest boronate. We pay attention to these stress tests, debugging batch quirks that show up only in advanced methods. This feedback cycle keeps our material fit for both classic flask chemistry and emerging technologies.
Lab staff and process chemists have shaped every improvement. A single phone call about filtration problems has prompted changes in drying procedures. Reports about color drift in stored samples led us to adjust antioxidants and packaging techniques. Real-time, field-driven updates guide our approach every quarter. We encourage feedback in any form—short emails, side notes at conferences, or formal reviews—because the chemistry never sits still, and neither can our workflow.
From startup biotechs to multinational pharma, research labs increasingly demand large-scale, reliable supplies of advanced boronic esters. Being at the source, we regularly handle questions about scalability, stress reactions, and process windows. We share solvent compatibility studies and mixing details openly with our partners, not holding knowledge back for competitive advantage. Our focus sits on enabling clients to de-risk their synthetic plans with data and transparent process support. This direct technical exchange sets manufacturing support apart from simple distribution.
Chemistry nerds at heart, our own R&D team experiments with new ligands, catalysts, and catalyst supports for the Suzuki-Miyaura reaction. Each time a new innovation emerges, we stress-test our 2-fluoropyridine-5-boronic acid pinacol ester on these protocols before clients ever ask. We’ve explored options like alternative boronic ester partners, custom fluorine placement, and chiral variants with our synthesis group, always asking if a tweak improves user results. Not every change sticks, but these trials mean we show up prepared when the next research avenue demands a slightly different building block or unexpected selectivity.
In a market crowded by similar-sounding boronic reagents, distinctive characteristics rise to the surface. Handling stability makes our pinacol ester far less fussy during storage than bare boronic acids or lesser-protected analogs. The electron-deficient pyridine ring with a fluorine substituent alters both its reactivity and its performance in couplings. During direct head-to-head tests, we’ve seen our ester outperform both non-fluorinated boronates and less-robust esters for demanding reactions. This matters to medicinal chemists and material scientists designing the next generation of functional molecules—there’s less ambiguity and more reliable synthetic outcome.
Few routine actions escape notice in real production. Controlling water content, checking glassware cleanliness, or even air flow during drying make their mark on final purity. We train new operators not only in procedures but in context, sharing experiences about how a stray spot of moisture or micro-impurity can propagate through a multistep synthesis, damaging yield and trust. Our own investment in maintaining high standards grows from a clear signal: the chemists who buy our product won’t accept excuses. They rely on us to deliver not on paper, but in flask and vial.
Each batch faces risks beyond nonconformance. Unpredictable exotherms or subtle trends in reagent quality might seem small but can compound under industrial scales. By layering on-line analytics and staged risk reviews, we address these challenges swiftly. Staff walk the floor with eyes open for small process drift, and backup protocols allow for rapid containment of off-spec material. These habits reflect cultural lessons passed down through years of production, learning as much from rarely-occurring problems as from daily routines.
Moving beyond internal QA, we value collaborative troubleshooting. Private knowledge stays with a single team, but discussion brings out better solutions, from filtration tweaks to in-process monitoring advances. Our partnerships with end users and peer manufacturers spark new ideas, creating tools for characterization or procedures that tighten selectivity even further. If another manufacturer shares a practical improvement for 2-fluoropyridine derivatives, we adopt, adapt, and report results. The industry’s success rides on shared gains.
We see direct impact when clients transition from intermediate aggregator sources to a manufacturer like us. Problem-solving speed improves, and clarity around quality and logistical support sharpens. Real chemistry knowledge sits on our floors, ready for hands-on troubleshooting or the next wild challenge from the lab. We push ourselves to deliver more than specification sheets, aiming to translate raw material into finished research success with every batch. The origin of your chemicals sets the standard for everything that follows.
Industrial manufacturing keeps shifting as both regulatory standards and research priorities change. Staying ahead requires constant monitoring of new reaction trends, green chemistry innovations, and regulatory developments impacting boronic ester handling. Our own environmental footprint keeps shrinking, and we adjust procedures as new technologies emerge. Processes pioneered in our labs often end up as best practices across client plants, continuing a cycle of innovation that benefits everyone.
The role we play in producing 2-fluoropyridine-5-boronic acid pinacol ester means more than putting powder in bottles. Every gram reflects a chain of decisions, lessons from feedback, and an ongoing conversation with chemistry’s next frontiers. Our pride in manufacturing this compound draws from every successful reaction reported by our customers and every fix delivered before a problem could slow down a research group’s progress. The future looks bright for those who respect both the science and the craft of this fine molecule. Let’s see what we can build, together, from the simplest ring and the most reliable boronic ester.