|
HS Code |
953122 |
| Iupac Name | 2,6-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine |
| Cas Number | 1267791-91-4 |
| Molecular Formula | C11H14BF2NO2 |
| Molecular Weight | 241.04 |
| Appearance | White to off-white solid |
| Smiles | B1OC(C)(C)C(C)(C)O1c2cc(F)nc(F)c2 |
| Synonyms | Pinacol 2,6-difluoropyridin-4-ylboronate |
| Solubility | Soluble in organic solvents (e.g., DMSO, THF) |
| Purity | Typically ≥ 97% |
| Storage Temperature | 2-8°C |
As an accredited 2,6-Difluoropyridine-4-boronic acid, pinacol ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 5-gram amber glass vial with a screw cap, clearly labeled for laboratory use and safety. |
| Container Loading (20′ FCL) | 20′ FCL container loaded with securely packaged 2,6-Difluoropyridine-4-boronic acid, pinacol ester; moisture- and contamination-protected. |
| Shipping | 2,6-Difluoropyridine-4-boronic acid, pinacol ester is shipped in tightly sealed containers under ambient conditions. The packaging ensures protection from moisture and light. It is classified as a non-hazardous chemical for transport, but standard laboratory chemical handling and shipping protocols are followed to ensure safe delivery and compliance with regulatory guidelines. |
| Storage | 2,6-Difluoropyridine-4-boronic acid, pinacol ester should be stored 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. Store at temperatures between 2–8°C (refrigerator). Keep away from oxidizing agents and acids. Properly label and handle according to standard laboratory safety protocols. |
| Shelf Life | 2,6-Difluoropyridine-4-boronic acid, pinacol ester typically has a shelf life of 1–2 years under cool, dry, and inert conditions. |
|
Purity 98%: 2,6-Difluoropyridine-4-boronic acid, pinacol ester with 98% purity is used in Suzuki-Miyaura cross-coupling reactions, where it ensures high catalytic efficiency and product yield. Melting Point 84-87°C: 2,6-Difluoropyridine-4-boronic acid, pinacol ester with a melting point of 84-87°C is used in automated solid-phase synthesis, where it provides reliable thermal processing and handling. Molecular Weight 269.06 g/mol: 2,6-Difluoropyridine-4-boronic acid, pinacol ester of 269.06 g/mol is used in medicinal chemistry library construction, where it offers precise molecular incorporation and reproducible results. Stability Temperature up to 40°C: 2,6-Difluoropyridine-4-boronic acid, pinacol ester stable up to 40°C is used in process development, where it allows for safe storage and uninterrupted synthetic workflows. Particle Size <50 μm: 2,6-Difluoropyridine-4-boronic acid, pinacol ester with particle size under 50 μm is used in high-throughput screening, where the fine granularity enhances reaction homogeneity and compound distribution. Solubility in DMSO: 2,6-Difluoropyridine-4-boronic acid, pinacol ester with high solubility in DMSO is used in parallel synthesis applications, where it enables uniform reagent dissolution and efficient reaction kinetics. |
Competitive 2,6-Difluoropyridine-4-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!
Every batch of 2,6-difluoropyridine-4-boronic acid, pinacol ester represents more than a chemical product on the shelf. Years spent perfecting synthesis and purification let us offer material that meets the expectations of advanced pharmaceutical, agrochemical, and specialty research teams. By manufacturing it ourselves, control stays with the process from raw material selection straight through to final QC release. We stand behind the actions and choices of our technical staff. The benefit, in plain words, is reliability. At no point in production do we hand off control. Our fluorination and boronation lines are set up for safe, clean, repeatable output, using closed systems and continuous feedback monitoring.
This ester is a frequent request among customers developing new medicinal compounds or exploring functionalized heteroaromatic architectures. The two fluorine atoms at 2 and 6 on the pyridine ring boost electron-withdrawing character, which shifts both reactivity and final compound properties. Attaching pinacol boronic acid moieties enables Suzuki-Miyaura coupling—a mainstay for carbon-carbon bond construction in drug and materials discovery. We see chemists reach for this intermediate for more than simple building block reasons. Fluorinated pyridines often yield enhanced metabolic stability and stronger receptor binding in bioactive targets, so this compound finds its way into the early hit-to-lead work that can eventually underpin market launches.
We keep current with the needs of our partners in pharma and chemical R&D. Material leaves our factory typically as a white to off-white solid. Analytical controls include HPLC purity above 98 percent and NMR confirmation for substitution patterns both in the ring and at the boronic pinacol position. Moisture control is no afterthought; batches undergo both Karl Fischer and loss on drying at regular intervals, ensuring no residual water compromises downstream coupling. Standard packaging is multiple-layer sealed bags or amber glass, since exposure to air or light could degrade sensitive inventory. Sample quantities range from grams for early studies to multi-kilo lots for scale-up, without dilution of quality standards.
This molecule shows up in labs working on kinase inhibitors, fluorinated agrochemicals, and advanced materials. Our internal team—often called on to troubleshoot coupling or isolation challenges—has handled enough scale-up runs of Suzuki chemistry to know real-world pain points. Common learning: minor differences in purity or residual solvents can disrupt coupling yields or cause downstream crystallization to crash. Having consistently high-purity batches means that methods dialed in at gram scale still translate to multigram or larger, without a string of failed pilot lots. In project work, using unreliable sources leads to guessing games in root-cause investigations; producing our own compound cuts down wasted cycles in problem solving.
Not all boronic esters act the same. For developers who typically source unsubstituted or mono-fluorinated pyridine boronic esters, the 2,6-difluoro derivative brings unique value. The electron-withdrawing influence alters both the site and velocity of coupling; selectivity can improve, and by-products reduce. In our direct experience, Suzuki reactions that stall with lower-substituted analogs show clear improvement here—not just on paper, but in flask and reactor. By comparison, pinacol-protected boronic acids offer better shelf stability than plain boronic acids, side-stepping the common dehydration or self-condensation pitfalls that sometimes shut down a reaction mid-run.
Making a boronic ester of this type brings its own set of production quirks. We learned early that vigorous exclusions of water and oxygen don’t just pad purity numbers—they support consistently robust yields and longer storage life. Scalable fluorination requires careful control of both temperature and reagent dosing. When temperatures run too hot, unwanted side products form. We invested in process development that includes real-time monitoring, not simply end-point checks, so data supports every run. The pinacol protection step undergoes careful pH monitoring; variance here causes impurity drift noticeable even by color. We resolved packaging and shipping logistics by using heavy-wall vessels and inert-atmosphere liners. Small adjustments like these add up to fewer customer complaints and better downstream results.
Years collaborating with pharmaceutical R&D taught us how crucial early-stage reliability is. Missed coupling steps or columns clogged with impurities add wasted weeks. Our production staff tailors each lot for immediate use in cross-coupling screens, fragment elaboration, and combinatorial libraries. Feedback from medchem teams led us to optimize for consistently low residual metals, addressing regulatory and technical concerns in final APIs. Agrochemical researchers exploring crop protection molecules value the consistent electron-withdrawing profile, as minute variations impact biological screening. In advanced materials sectors, those pushing new fluorinated organic electronic scaffolds also highlight stable purity and batch homogeneity.
Researchers have reached out about sluggish reactivity or unexpected by-products in their coupling work. We dove back into our own experiments and found elevated moisture at the user site drove most of the issues—pinacol boronic esters scavenge water, harming downstream reactions. Packing in atmosphere-controlled environments and rapid shipping cut out many of these complaints. Another common snag: compatibility with other polar functional groups. Paying attention to three-point purity—boronic ester, fluoropyridine, and pinacol content—means most customers see predictable LC-MS profiles in their coupled products. Early transparency about solvent and trace metal profiles prevents later scale-up headaches. An open line from our technical support team—engineers and chemists, not just customer service—helps troubleshoot user-specific quirks rapidly by comparing on-lab findings with our own pilot data.
Boronic esters and fluorinated intermediates require robust safety protocols. We take environmental discharge and staff exposure seriously. Factory lines operate closed, with HEPA filtration catching fine solids and solvent recovery units recycling up to 80 percent of process materials. The obligatory PPE is more than just a sign on the wall; regular safety audits and ongoing staff training underpin our process. Shipping to customers follows both hazmat and environmental regulations—product containers lock down in secondary containment, with full traceability from docking to end-user lab.
2,6-Difluoropyridine-4-boronic acid, pinacol ester enables labs to focus on their chemistry rather than re-source, re-test, or trouble-shoot intermediates. As the original manufacturer, we bypass common pitfalls such as inconsistent supply, suspect re-packaging, or the mystery of off-brand origins. By keeping manufacturing in-house, adapting continuously based on user feedback, and policing each lot, every batch we ship reflects the lessons of previous runs and the expectations of future projects. Customers return for scale-up fit and project continuity, not just price. Direct lines to our synthesis team let development chemists get nuanced details—ranging from safe solvent choices in scale-up to tips on avoiding hydrolytic degradation—without waiting for a chain of third parties to pass questions along.
We source our raw materials from proven suppliers known for transparency in their own sub-contracting. Regulatory and compliance needs drive us to trace every container back to its point of origin, with documentation ready for audits and regulatory review. By remaining in direct touch with regulatory updates for GMP and REACH-related guidance, our team responds quickly to cross-border shipments or ON-site audits from major pharma partners. Full batch records, including analytical, process, and safety components, are maintained not just for compliance, but to help users scale from discovery to commercial production with confidence.
New sectors emerge each year looking for this type of fluorinated aromatic boronic ester. We track patent filings and market developments in custom electronics, smart materials, and more complex agrochemical targets. Our development chemists regularly benchmark against both regional and international competitors; any drift in key metrics—impurity levels, coupling efficiency, or user-reported side-product formation—drives process improvement or foucses future R&D cycles. By staying close to both upstream and downstream partners, we align future capacity and logistics with new demand without delay or resource overstretch.
Getting 2,6-difluoropyridine-4-boronic acid, pinacol ester straight from the actual manufacturer, rather than traders or brokers, cuts out risk. We have nothing to hide about our process or ingredient chain. If post-shipping storage needs change, or if a user wants to switch from glass to polymer vessel, we answer fast and adjust, sometimes on-the-fly. Our senior technical teams review each customer complaint, troubleshoot issues in tandem, and pass those lessons straight back into the next set of runs. Loyalty from high-growth biotech and Fortune 500 clients builds not just on price or paperwork, but on solving problems together and supporting their launches downstream.
Process improvement has no finish line. Even years after standardizing this boronic ester, we revisit purification, solvent recapture, and shipping timelines. The goal: shave off small sources of impurity or waste, feed R&D with fresh data, and align with shifting regulatory and safety demands. Our process engineers attend technical forums and contribute to chemical manufacturing roundtables, benchmarking internal data against field-wide best practices. Direct feedback from users in pharma, agro, and advanced materials motivates continuous upgrades—both to the production facility and the analytical suite.
Trust forms the core of any supply relationship, especially in custom or technically demanding intermediates. We handle each batch as if it would be used in our own discovery process, with chemical engineers and quality managers sharing responsibility every step of the way. Clients always have full batch-level traceability at hand. By fostering close partnerships and transparent communication, our customers know exactly what goes into their projects—and how to keep them moving.
Chemists who use 2,6-difluoropyridine-4-boronic acid, pinacol ester sometimes reach a point where a unique issue or application needs new approaches. By connecting directly with our formulation and manufacturing personnel, constructive dialogue bypasses layers of generic advice. Real accounts from our staff about scale-up pitfalls, storage tips, or unusual coupling bottlenecks shape a better outcome for everyone. Technical mastery comes from ongoing exposure to both the molecule and the process, and our team recognizes that each customer's challenge sharpens our methods further.
Long experience making this compound in house supports repeat supply and ongoing project builds. Repeat collaborations with leading research labs and industrial users create a feedback loop that sharpens every step of our process. Users handling kilo-lot or just-in-time shipments benefit from streamlined logistics—direct from plant to bench, without repack or unnecessary redistribution stops. Shared experience also means user feedback informs how we refine particle size for easier handling, or scale up runs without introducing new impurities. It’s more than just supply—it’s a partnership geared towards advancing your science, supported by a solid foundation in practical chemical manufacture.
As a chemical manufacturer, our history, hands-on knowledge, and direct accountability give every user of 2,6-difluoropyridine-4-boronic acid, pinacol ester a clear advantage. Consistency, transparency, readiness to adapt, and continuous learning form the DNA of our team. With every new lot and every solved challenge, we reinforce the partnership between producer and research community, confident that success in your downstream projects starts with the right chemistry—produced, tested, and delivered by people who understand both its potential and its practical realities.