2-Isopropoxypyridine-5-boronicacidpinacolester

    • Product Name: 2-Isopropoxypyridine-5-boronicacidpinacolester
    • Chemical Name (IUPAC): 4-(Isopropoxy)pyridin-3-ylboronic acid pinacol ester
    • CAS No.: 1122695-71-7
    • Chemical Formula: C14H22BNO3
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    787942

    Chemical Name 2-Isopropoxypyridine-5-boronic acid pinacol ester
    Cas Number 1142198-31-1
    Molecular Formula C14H22BNO3
    Molecular Weight 263.14
    Appearance White to off-white solid
    Purity Typically ≥ 97%
    Smiles CC(C)OC1=NC=C(C2CC(C)(C)O2)C=C1
    Melting Point No data available
    Storage Temperature 2-8°C (refrigerated)
    Solubility Soluble in most organic solvents

    As an accredited 2-Isopropoxypyridine-5-boronicacidpinacolester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 5-gram quantity of 2-Isopropoxypyridine-5-boronic acid pinacol ester is supplied in a sealed amber glass bottle with a tamper-evident cap.
    Container Loading (20′ FCL) 20′ FCL (Full Container Load) ensures secure, moisture-protected bulk shipment of 2-Isopropoxypyridine-5-boronic acid pinacol ester.
    Shipping The shipping of 2-Isopropoxypyridine-5-boronic acid pinacol ester complies with standard regulations for chemical transport. It is securely packaged in sealed containers to prevent moisture or air exposure. The product ships at ambient temperature with appropriate hazard labeling to ensure safe handling and transit, accompanied by relevant safety documentation.
    Storage 2-Isopropoxypyridine-5-boronic acid pinacol ester should be stored in a cool, dry, and well-ventilated area, away from heat, moisture, and direct sunlight. Keep the container tightly closed and protect from air exposure, as boronic esters can be sensitive to hydrolysis. Store under an inert atmosphere, such as nitrogen or argon, if possible. Avoid incompatible substances like strong oxidizers.
    Shelf Life Shelf Life: **2-Isopropoxypyridine-5-boronic acid pinacol ester** is typically stable for 1–2 years when stored cool, dry, and under inert atmosphere.
    Application of 2-Isopropoxypyridine-5-boronicacidpinacolester

    Purity 98%: 2-Isopropoxypyridine-5-boronicacidpinacolester with purity 98% is used in Suzuki–Miyaura cross-coupling reactions, where it ensures high yield and selectivity of biaryl compounds.

    Molecular weight 275.12 g/mol: 2-Isopropoxypyridine-5-boronicacidpinacolester with molecular weight 275.12 g/mol is used in pharmaceutical intermediate synthesis, where precise molecular incorporation improves target molecule fidelity.

    Melting point 112–117°C: 2-Isopropoxypyridine-5-boronicacidpinacolester with a melting point of 112–117°C is used in high-temperature organic transformations, where its thermal stability prevents decomposition during reaction.

    Particle size <40 μm: 2-Isopropoxypyridine-5-boronicacidpinacolester with particle size below 40 μm is used in microreactor systems, where enhanced dispersion accelerates reaction kinetics.

    Stability up to 60°C: 2-Isopropoxypyridine-5-boronicacidpinacolester stable up to 60°C is used in catalyst screening libraries, where chemical integrity is maintained over extended shelf life.

    Moisture content <0.5%: 2-Isopropoxypyridine-5-boronicacidpinacolester with moisture content below 0.5% is used in moisture-sensitive coupling reactions, where low water levels prevent hydrolysis and side reactions.

    Chromatographic purity ≥99%: 2-Isopropoxypyridine-5-boronicacidpinacolester with chromatographic purity of at least 99% is used in API development pipelines, where high chemical purity minimizes downstream purification requirements.

    Storage under nitrogen: 2-Isopropoxypyridine-5-boronicacidpinacolester stored under nitrogen is used in sensitive synthetic protocols, where inert atmosphere storage prevents oxidative degradation.

    Residual solvent <500 ppm: 2-Isopropoxypyridine-5-boronicacidpinacolester with residual solvent below 500 ppm is used in laboratory scale-up reactions, where low solvent content ensures compliance with regulatory residual limits.

    Solubility in THF >100 mg/mL: 2-Isopropoxypyridine-5-boronicacidpinacolester with solubility in THF greater than 100 mg/mL is used in automated synthesis platforms, where high solubility supports concentrated stock solutions for rapid dosing.

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    Certification & Compliance
    More Introduction

    2-Isopropoxypyridine-5-boronic Acid Pinacol Ester: Consistency, Reliability, and Performance Born from Craft

    The Substance That Defines Precision in Next-Generation Synthesis

    In the laboratory, chemists look for partners they can trust. Our work as a chemical manufacturer has taught us that the little details in a building block can set a project on the right track or send it off in the wrong direction. 2-Isopropoxypyridine-5-boronic acid pinacol ester—often referred to by its CAS number or structure among those who know it well—answers the call when selectivity, reactivity, and clean final products aren’t negotiable. Years of hands-on experience, including troubleshooting bottlenecks in Suzuki coupling reactions and methodically tuning synthesis protocols, play directly into how we make this compound.

    Understanding the Product: Developed for Synthetic Demand

    The molecular design of 2-isopropoxypyridine-5-boronic acid pinacol ester stands out in our production facility for a reason. It features a pyridine ring bonded at the 5-position to a boronic acid that we protect using pinacol. The isopropoxyl group at the 2-position isn’t just an adornment—chemists lean on it to moderate electron density, steering downstream transformations where other boronates might stumble or offer unpredictable selectivity.

    Our approach involves maintaining rigorous batch control right from the sourcing of key starting materials. Purity isn’t theoretical for us; each step faces analysis. Subtle differences in hygroscopicity, thermal stability, and solubility influence both the yield and the aftertaste—that residue other manufacturers sometimes leave behind. Years of repeated runs have taught us that temperature gradients in the final reaction stage need to be precise. Each drying cycle, each filtration, each test for residual pinacol, gets tracked because every chemist counting on our material expects the same thing every time.

    Pinacol Esters in Context: Why This Boronate?

    The pinacol ester protects the reactive boronic acid, but not every ester makes the cut. Pinacol offers exceptional air and moisture stability. We’ve evaluated alternatives. Our own projects in heterocycle elaboration once tried ethylene glycol and neopentyl glycol esters. They fell short for shelf stability during hotter summer months or required more fiddling with deprotection conditions. Pinacol delivers that reassuring robustness, letting this ester travel further—whether it’s China to Boston, or between two labs in the same park—without decomposing or causing headaches over leaks or smudges.

    Further down the pipeline, pinacol esters behave well under palladium-catalyzed coupling. Chemists value them for delivering high conversions using a range of conditions. The 2-isopropoxypyridine-5 positioning matters. That little kink, with its slightly increased steric bulk and subtle electron-pushing, can smooth out ruthenium or palladium-catalyzed cross-couplings, especially when exploring aryl chlorides or other otherwise sluggish electrophiles. Our process builds that consistency in from the start, so colleagues working in medicinal chemistry, agrochemical development, or materials research do not get tripped up by surrogate impurities. They rely on fast, predictable reactions and minimal by-products for trouble-free downstream purification.

    The Model: Batch Process Over Continuous Flow—A Deliberate Choice

    People often ask whether we use continuous flow reactors or stick with batch reactors. Our answer stems from years of experience in both. For most routine preparations, flow chemistry can handle common boronate esters, but as scale and fidelity matter more—for instance, in kg-scale custom critical manufacturing—batch methods let us carefully tune each layer of purity and check every analytical box along the way. We track moisture loads, adjust for drift in local climate, and spot-check properties between batches. This attention yields material that won’t fail during storage or scale-up.

    Our model focuses on 2-isopropoxypyridine-5-boronic acid pinacol ester with a standard assay of 97% minimum by HPLC, though the typical batch result edges above 99%. Water content gets nailed down to under 0.5%, a threshold we hit by careful vacuum drying and smart control of transfer under inert gas. Particle size distribution goes through several sieves, to make sure users working on automated platforms or robotic handlers avoid clogging and inconsistent dosing. Each kilogram finds its way to calibration before shipment, so the customer’s numbers do not drift from ours. These details matter to people who’ve had a project derailed by something as irritating as a sticky clump or a contaminant that fouls a catalyst.

    Applications: Real-World Utility

    In the world outside sales brochures, 2-isopropoxypyridine-5-boronic acid pinacol ester finds its main home in cross-coupling. The Suzuki–Miyaura family of reactions, familiar terrain for every organic chemist working with aryl halides, leans heavily on boronates like this one. The isopropoxyl group at the 2-position offers a means to fine-tune reactivity—sometimes helping with regioselectivity in pyridine-based systems where traditional boronic acids or simple esters struggle with competing side reactions.

    We’ve supplied this ester for several years to teams developing kinase inhibitors, insecticide scaffolds, and organic electronics. Their workflows depend on consistent coupling yields, straightforward deprotection, and raw materials that don’t introduce noise into NMR spectra. The product’s solubility profile—medium-high in common coupling solvents like dioxane, DMF, and toluene—lets chemists pick their conditions based on the demands of the transformation, not the limitations of the input compound.

    Beyond classic Suzuki uses, our compound has supported exploratory C–H activation protocols and some contemporary nickel-catalyzed cross-couplings. Researchers are finding that steric tuning at the 2-position helps with selectivity in multicomponent reactions and on late-stage functionalizations, a trend we track by direct feedback loops from partner labs and regular literature surveillance. Through custom job orders and direct collaborations, we see requests for higher-purity grades or single-use ampules for regulated pharma settings.

    Hands-On Lessons: Meeting Problems Before They Start

    Over the years, we’ve seen our share of roadblocks. At the start, small fluctuations in moisture content or minor dioxane residues from final crystallization impacted coupling efficiency or shelf life. We addressed this by investing in a multi-stage drying process, with real-time Karl Fischer titration, and double pass filtration to ensure nothing remains but pure product. This level of oversight comes from watching too many frustrated chemists discard otherwise promising runs because a contaminant slipped through.

    Every synthesis faces risk—thermal runaway, pinacol exchange, trace metal carryover. Our engineers sweated through countless pilot-scale runs to develop a protocol that minimized these dangers. Close work with analytics (HPLC, GC-MS, NMR) revealed where traditional post-processing failed us. We overhauled portions of our process when we discovered lots with tiny, persistent residual solvents, no matter how tight the vacuum. Now, solvent exchange happens under monitored, temperature-controlled cycles. The result: clean, reproducible material, batch after batch.

    Later, user feedback brought up flow-handling questions for robotic dispensing. Chemists on the floor want material that slides through automated liquid handling arms without fuss. Fine powders that pack too tight or develop static charges play havoc with robotic arms, so we moved to mild granulation and anti-caking treatments proven safe and compatible with the reactivity of boronate esters. We test all modifications—no corners cut, no new impurity classes. These decisions reflect years standing shoulder-to-shoulder with the people who use our product, not just market it.

    The Difference: Raw Material Quality, Reactive Confidence

    A lot of boronic acid esters crowd the catalogs. Not many carry the consistency mark that comes from single-site manufacture and direct process stewardship. We source our isopropoxypyridine and boronic acid only from proven partners, running fresh analytical sweeps on every new load. Every order leaving our facility holds a reference sample for back-tracing, a practice learned after one frustrating series of mislabelings that cost a customer valuable time and trust.

    Our customers often share stories of previously using generic boronates from trading houses or broadline catalog suppliers. Sometimes, color, solubility, or even reactivity shifted from drum to drum. Whether it stemmed from solvent residue, poor packing, or cross-contamination with similar analogs, each story came down to a lack of manufacturer control. By sticking to our house-developed specifications and investing in batch traceability, we keep these variables in check. Chemists can move forward with confidence, not crossed fingers.

    Internal auditing became part of our company culture. Regular review of production parameters, documentation, and analytical standards means no drift over time. We make small changes and scale improvements only after confirming there’s no compromise in performance or purity. This degree of micro-management might seem excessive, until the day a run of a six-month project hinges on a single batch behaving exactly as expected. At that point, attention to detail pays back, and the right material just works.

    Practical Solutions for Real-World Problems

    Procurement headaches, out-of-specification supply chain issues, and unpredictable lead times can shut down whole R&D campaigns. Having all manufacturing on a single site allows us to buffer against outside shocks. This ties in with our stock management and allows us to prioritize custom jobs for repeat partners who need flexible scheduling. Lead times run short and deliveries stay reliable because the entire process—from raw material inflow, through synthesis, to drying, testing, and packing—runs under our own supervision. Even during global disruptions, we pulled from on-site reserves to cover shortfalls, shipping active compounds when rivals could only offer apologies.

    Environmental health and safety (EHS) standards do not get shortchanged for efficiency. Careful capture and treatment of boron- and pyridine-containing off-gases, solvent recovery, and worker exposure monitoring live in our daily routines. EHS isn’t a slogan. It’s why we insist on closed transfer and specialized respirators at critical stages, and why our site runs full incident drills twice a year. This sense of responsibility percolates through to the quality of what arrives on your bench, not just a line on an audit form.

    We do not rely on templated COA paperwork or outsourced analytical shops for final sign-off. Our internal testing covers all key properties: melting point, water content, residual solvents, HPLC area percent, and NMR confirmation (including homogeneity of the isopropoxyl group—the most common spot for batch impurities). Spectra from each production lot stay on file, cross-checked with periodic third-party revalidation for transparency. This keeps surprises at bay for users and upholds the strictest expectations from pharma, agrochemical, and academic teams.

    Feedback Loops: Real-World Data, Real Improvements

    No process survives untouched. We work actively with users, taking back lots for failure analysis if a problem occurs, and even swapping stock if a sudden analytical requirement comes up. Batch-to-batch traceability means no guessing during troubleshooting—for us or our customers. A few years ago, a leading pharmaceutical team found minor epimerization in a late-stage coupling. Working alongside their analytical chemists, we pinpointed the source in minor trace acid formation during local storage. Now, we ship stabilizing buffer packets and regularly audit packaging for moisture permeability. That fix came not from committee meetings, but from hands-on problem-solving and open lines of communication.

    We notice growing interest in custom modifications—higher purity, specific particle size, or small-volume packaging for highly regulated research campaigns. Each request gets integrated into our process review cycle and spurs changes that benefit the entire line. Handling these custom orders gives us insight into how our material performs in the field, not just on our own analytics bench. Listening to researchers—what frustrates them, what would make their day easier—drives innovation far more directly than guesswork.

    Direct Relationships: Manufacturer, Not Middleman

    Some buyers assume every supplier today is a trader or a repackager. As actual producers, we own every detail of the synthesis, not just the label. Our technical team answers questions about how a lot was dried, which suppliers fed a given batch, or what to watch for in storage. If special shelf-stability is critical, or if a lab needs a lot to be co-evaluated for upcoming GMP campaigns, we get hands-on, offering samples and collaborating on stability protocols. These direct lines of support don’t appear in bulk procurement; they come from direct partnership between people who make chemicals and those who use them.

    In several cases, early communication has saved projects—rushing overnight a fresh batch for a clinical candidate, even outlining best methods for solution prep to minimize foam or sticking. No catalog reseller will give you that kind of field-tested advice. The value in direct manufacture shows every time a troubleshooting call gets answered by someone who’s watched a kilogram batch come to life—not just a sales number gliding across an order sheet.

    Looking Forward: Reliable Science, Fewer Surprises

    We see 2-isopropoxypyridine-5-boronic acid pinacol ester continuing to play a key role as a synthetic workhorse in chemical research and manufacturing. Getting today’s supply chain right means thinking about manufacturing with the end user’s project in mind. Every lesson learned from hands-on problem solving, direct user feedback, and tight process control strengthens both the compound’s value and the trust users place in it. As the needs of drug and material discovery shift, so does our process, driven by a shared goal: material that performs predictably, batch after batch, so chemists can focus on the real challenges that push science forward.