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HS Code |
548082 |
| Product Name | 2-Methoxy-5-fluoropyridine-4-boronic acid |
| Cas Number | 1211595-13-9 |
| Molecular Formula | C6H7BFNO3 |
| Molecular Weight | 170.94 |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Solubility | Soluble in DMSO and methanol |
| Smiles | B(C1=CC(=NC=C1F)OC)(O)O |
| Inchi | InChI=1S/C6H7BFNO3/c1-12-6-4(7(10)11)2-3-8-5(6)9/h2-3,10-11H,1H3 |
| Synonyms | 5-Fluoro-2-methoxypyridine-4-boronic acid |
| Storage Conditions | Store at 2-8°C, protected from moisture |
| Application | Organic synthesis, Suzuki coupling |
As an accredited 2-Methoxy-5-fluoropyridine-4-boronic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 5-gram amber glass bottle, screw-capped, labeled "2-Methoxy-5-fluoropyridine-4-boronic acid" with hazard and lot information. |
| Container Loading (20′ FCL) | 20′ FCL for 2-Methoxy-5-fluoropyridine-4-boronic acid: Securely packed in drums, moisture-protected, with clear labeling and documentation, suitable for export. |
| Shipping | **Shipping Description for 2-Methoxy-5-fluoropyridine-4-boronic acid:** This chemical is shipped in a tightly sealed container, protected from moisture and light. Transport follows standard laboratory chemical regulations. Handle with appropriate safety precautions. Temperature-sensitive; avoid extreme temperatures during transit. Accompanied by a safety data sheet (SDS) and compliant with international shipping guidelines. Not classified as hazardous for transport. |
| Storage | 2-Methoxy-5-fluoropyridine-4-boronic acid should be stored in a cool, dry, and well-ventilated area, away from sources of moisture and incompatible substances. Keep the container tightly closed and protected from direct sunlight. Store at 2-8°C if specified by the manufacturer. Handle under inert atmosphere if sensitive to air. Proper labeling and secure storage are recommended to prevent accidental exposure. |
| Shelf Life | Shelf life of 2-Methoxy-5-fluoropyridine-4-boronic acid: Stable for 1–2 years when stored dry, cool, and protected from light. |
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Purity 98%: 2-Methoxy-5-fluoropyridine-4-boronic acid with purity 98% is used in Suzuki-Miyaura cross-coupling reactions, where it enhances coupling efficiency and yields high-purity biaryl products. Stability Temperature 25°C: 2-Methoxy-5-fluoropyridine-4-boronic acid with stability temperature up to 25°C is used in storage and handling for pharmaceutical synthesis, where it maintains structural integrity and consistent reactivity. Particle Size <50 µm: 2-Methoxy-5-fluoropyridine-4-boronic acid with particle size less than 50 µm is used in catalysis research, where it provides rapid dissolution and uniform reaction kinetics. Melting Point 180-185°C: 2-Methoxy-5-fluoropyridine-4-boronic acid with melting point 180-185°C is used in solid-state formulation studies, where it ensures reliable thermal processing and product stability. Molecular Weight 200.99 g/mol: 2-Methoxy-5-fluoropyridine-4-boronic acid with molecular weight 200.99 g/mol is used in heterocyclic compound synthesis, where it offers precise molecular incorporation and reproducible results. Water Solubility <1 mg/mL: 2-Methoxy-5-fluoropyridine-4-boronic acid with water solubility less than 1 mg/mL is used in organic phase coupling, where it prevents premature hydrolysis and increases selectivity. |
Competitive 2-Methoxy-5-fluoropyridine-4-boronic acid prices that fit your budget—flexible terms and customized quotes for every order.
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On production lines where precision and consistency matter, each compound earns its place through a blend of chemical integrity and practical utility. As producers of 2-Methoxy-5-fluoropyridine-4-boronic acid, our experience has taught us not every boronic acid stands up to the real-world demands of pharmaceutical or fine chemical applications. This isn’t just another intermediate—its profile is the result of careful process design and persistent quality tuning.
The model consistently delivered from our reactors has a molecular structure (C6H7BFNO3) defined by its 2-methoxy and 5-fluoro substituents on a pyridine ring, coupled with a boronic acid group at the 4-position. Years of scale-up, repeated purification, and stress-testing have confirmed batch-to-batch reproducibility in both purity and physical characteristics.
Producing this compound might sound like just another routine for a boronic acid, but we know what our customers will face. Whether researchers set out to build complex small molecules or pharmaceutical leads, the difference between success and troubleshooting often traces back to the reliability of upstream intermediates. If the starting material brings unpredictable impurities or inconsistent melting points, yields drop, separation headaches follow, and costs climb—fast. We've seen how a higher-purity product pays back the investment in less wasted effort and shorter downstream purification.
Years ago, our R&D chemists noticed bottlenecks when scaling up heteroaryl boronic acid couplings. Not all substituted pyridine boronic acids handle Suzuki-Miyaura reactions equally—the presence of a 5-fluoro group, paired with 2-methoxy protection, can influence both reactivity and side-product formation. By refining our process, we’ve minimized common contamination by regioisomers or over-fluorinated analogs, both of which trouble subsequent steps.
From our perspective, any inconsistency—missed endpoint during crystallization, traces of starting pyridine, residual fluoride—means fielding complaints from colleagues downstream who rely on milligram-scale tests before committing to kilogram runs. Rigorous controls on temperature, stoichiometry, and solvent removal have been built into every batch, supported by daily hands-on monitoring rather than just paperwork sign-offs.
The demand for this compound comes largely from biopharma R&D, where aromatic boronates make trusted building blocks for constructing complex scaffolds, especially using palladium-catalyzed cross-couplings. What sets 2-Methoxy-5-fluoropyridine-4-boronic acid apart is the unique electronic interplay that the methoxy and fluoro groups impart, tweaking the reactivity compared to simple pyridine boronic acids or other fluorinated variants.
We learned early that not all laboratories want the same particle size. For scale-up, teams often request a coarser product that pours smoothly and resists clumping, making it easier to weigh and handle. Research groups working on rapid screenings in microwell plates often tell us they prefer more finely powdered material for fast dissolution and repeatable pipetting. Our reactors and milling lines accommodate both, so the specifications we deliver reflect how real-world users actually work, not just theoretical purity on paper.
A casual comparison of boronic acids sometimes misses what regular users notice after hundreds of runs. Some products tend to hydrolyze faster on the shelf; some generate haze in reaction mixtures, signaling byproducts or trace contamination. Through material stability studies and real-world feedback loops with chemists, we have adapted our process to prolong shelf life and minimize oxidative degradation—a real concern with organoboron reagents, especially for long-term inventory needs.
Fluorinated arenes in particular bring unique challenges. Conventional synthetic routes can leave behind subtle levels of unreacted fluoride or alternate positional isomers, which disrupt both coupling efficiency and analytical characterization of finished products. Our purification trains include stepwise crystallization, controlled temperature drying, and routine NMR, HPLC, and GC-MS analyses. This attention to detail limits “dark horse” impurities that can reappear after months in storage or under the stress of metal-catalyzed coupling.
Every kilogram shipped builds on the lessons of pilot batches. For example, pyridine-based boronic acids have a tendency to form hydrates, especially in the presence of atmospheric moisture. Early versions suffered from unpredictable weight loss on drying, frustrating chemists seeking to reproduce exact stoichiometries. We tightened controls on packaging and storage humidity, shifting to inert atmospheres and vapor-barrier containers after feedback from our pilot plant.
Solubility also stands out as a real-world concern. In high-throughput settings or multi-step synthetic routes, unpredictable solubility can slow batch processing or cause unexpected precipitation. This compound, with its methoxy and fluoro modifications, outperforms some analogues by dissolving faster in standard polar aprotic solvents—something our process engineers have validated repeatedly with customer teams developing clinical candidates.
While Suzuki-Miyaura couplings form the backbone of applications for this molecule, years of supply have shown us unexpected uses. Late-stage fluorination or methoxylation of complex molecules can be tricky; by integrating this building block early, chemists often simplify their downstream transformations. Additionally, the rigidification introduced by the pyridine ring, combined with programmable substituent effects, enables fine-tuning of the electronic environment in drug candidate molecules.
Our collaboration with medicinal chemists has revealed uses in materials science, especially for specialty ligands and heteroarene functionalization strategies. Each new direction leads to fresh demands on reproducibility—the best feedback comes not from one-off requests but from ongoing projects optimizing by the dozen.
Starter materials act as linchpins in any synthesis. Over time, analysts in our lab have learned which checkpoints matter most: melting range, color, moisture content, residual solvents, and boron/fluorine assay. We regularly analyze decay samples from archived batches stored for over a year, ensuring that what left our warehouse last season performs on par with today’s production.
We avoid short-cutting process validation, because every batch gone awry means not only lost hours but broken customer trust. Full documentation—spectra, lot records, process deviation logs—back what we ship. When a new request comes in for gram-to-kilogram lots, our documentation and past records confirm that standards haven't slipped. That discipline pays off downstream for clients who already navigate tight project timelines.
Emerging pharmaceutical targets often call for fluorinated heterocycles as core motifs, driving continued demand for intermediates that combine both electron-rich and electron-deficient substituents. The dual functionality in this compound—methoxy for electron donation and fluoro for electron withdrawal—sets up possibilities for selective activation in cross-coupling reactions.
From both strategic planning and daily lab reality, we see investment in further optimization as a must. Automation in solid-state characterization, inline NMR for faster release testing, and next-generation packaging for greater stability across climates all remain under review. Input from users working in green chemistry and low-waste methodologies drive our push for more efficient solvent recovery and minimized byproduct generation—factors that may not show up in a bottle of white powder, but play out in every cost calculation and project milestone downstream.
After years manufacturing specialty boronic acids, we’ve noticed the qualitative differences when chemists have direct access to our technical teams—and the data underlying each batch. Reps from distribution chains often aren’t equipped to explain performance deviations or suggest alternate packaging in response to process quirks. In contrast, direct conversations with chemists on our production floor, who have watched this material evolve from a bench curiosity to a trusted intermediate, surface logistical insights and troubleshooting help that real-world users value.
Custom variations often arise out of these discussions: tailored packaging suited to automated dispensing systems, alternate purification steps for lower residual solvents, bulk lot reservations to guarantee continuity of supply across lengthy projects. Our role isn’t just as producers but as partners, using the feedback loop between process engineers, QC labs, and end users to raise the bar for both performance and reliability.
High-quality boronic acids require active intervention, not just monitoring. After observing subtle shifts in melting ranges during several seasons, we traced the issue to minor changes in upstream solvent sourcing. Only by consistent batchwise cross-checks and quick process tweaks did we keep product quality from drifting—a clear reminder that even mature products demand ongoing vigilance, not set-it-and-forget-it mentality.
Internal stress-tests, benchmarking archival samples, and open lines of communication between synthesis and analytical teams keep us honest. This investment in transparency and improvement enables users to focus on their synthetic targets, not the reliability of their starting materials.
Clients have direct access to full COA and analytical spectra—NMR (1H, 13C, 19F, 11B), HPLC chromatograms, and GC-MS scans—which demonstrate identity and purity. Analytical chromatograms from real batches, not just “representative” ones, accompany every order. We recognize that informed clients spot inconsistencies early and provide key feedback for continual process improvement. Open sharing of spectral and analytical details—sensitive enough to expose even minor byproducts—encourages accountability and collaboration, not just transaction.
The continuous improvement loop includes upgrading reactor controls, refining dry room protocols, and regularly benchmarking against best-in-class analytical standards. Supply chain transparency adds value by setting clear expectations for both shipment timing and post-shipment support. Direct feedback on shipment quality, coordinated troubleshooting, and tailored handling instructions transform chemical supply from a commodity transaction into a productive partnership.
We noticed that successful projects tend to correlate with open, two-way communication on timelines, lot validity, and sample requests—a lesson that prompted us to invest in better digital tracking and reporting. This helps guarantee supply when researchers need it most and reduces bottlenecks when projects scale from grams to kilograms.
Customization requests test production agility: alternate particle sizes, custom blending, or specific solvent residues. In practice, extensive requests must be evaluated for potential trade-offs in batch size, homogeneity, or regulatory compliance. We weigh these decisions carefully, ensuring that every custom batch achieves the same analytical robustness as standard production runs. Choices are driven by concrete user requirements and direct feedback, not guesswork or market speculation.
Real-time adjustment depends on direct dialogue with application scientists. Informed by their priorities, our process engineers can recommend the right packaging, optimize drying methods, and plan coordinated shipping around project milestones. The back-and-forth guides how improvements roll out, ensuring process flexibility serves real laboratory needs, not simply theoretical possibilities.
Like any specialty manufacturer, we’ve weathered hits and misses, learning from every failed pilot batch or shipment rejected for minor specification drift. Each setback led to tangible process improvements—faster in-process analytics, tighter supplier vetting, clear batch records, or expanded input from end users across research and manufacturing. These lessons shape our operational philosophy: proactive troubleshooting, meticulous process control, and full data transparency.
The reality in modern chemical manufacturing is that no route or process stays static for long. Methodologies evolve, analytical tools advance, and application scientists constantly raise expectations. Instead of guessing at demand, we keep our development loop tight, so every change improves reliability and reproducibility.
Ultimately, the success of research and manufacturing projects using 2-Methoxy-5-fluoropyridine-4-boronic acid hinges on the quiet reliability of the input chemicals. We know from years supplying pharma and materials science teams that every extra purification step, every unplanned analytical intervention, steals time and budget from the true challenge—making new breakthroughs in molecular science.
By anchoring our process in hands-on experience, continuous analytical verification, proactive process improvements, and real-world user feedback, we deliver more than a molecular name. Our product serves as a foundation for successful synthetic projects, validated by those who depend on it for daily research and production. Reliability starts on our shop floor, but it pays off in breakthroughs achieved by the research groups and manufacturers—who count on us for more than a catalog entry.