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Phenol, 3,5-Difluoro-4-[5-(1-Methylethyl)-1,2,4-Oxadiazol-3-Yl]-

Phenol, 3,5-Difluoro-4-[5-(1-Methylethyl)-1,2,4-Oxadiazol-3-Yl]-


    • Product Name Phenol, 3,5-Difluoro-4-[5-(1-Methylethyl)-1,2,4-Oxadiazol-3-Yl]-
    • Alias 3,5-Difluoro-4-[5-(propan-2-yl)-1,2,4-oxadiazol-3-yl]phenol
    • Einecs 809-457-4
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
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    Specifications

    HS Code

    654084

    Chemical Name Phenol, 3,5-Difluoro-4-[5-(1-Methylethyl)-1,2,4-Oxadiazol-3-Yl]-
    Molecular Formula C11H10F2N2O2
    Molecular Weight 240.21 g/mol
    Cas Number 1368256-73-8
    Appearance Solid (presumed, based on structure)
    Smiles CC(C)c1nc(no1)c2c(c(c(c(c2)F)O)F)
    Synonyms 3,5-Difluoro-4-[5-isopropyl-1,2,4-oxadiazol-3-yl]phenol
    Pubchem Cid 137181222
    Inchi InChI=1S/C11H10F2N2O2/c1-6(2)10-14-11(17-15-10)7-4-8(12)9(16)5-3-7(13)9/h3-6,16H,1-2H3

    As an accredited Phenol, 3,5-Difluoro-4-[5-(1-Methylethyl)-1,2,4-Oxadiazol-3-Yl]- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle with a secure screw cap, clearly labeled: “Phenol, 3,5-Difluoro-4-[5-(1-Methylethyl)-1,2,4-Oxadiazol-3-Yl]-.”
    Shipping **Shipping Description for Phenol, 3,5-Difluoro-4-[5-(1-Methylethyl)-1,2,4-Oxadiazol-3-Yl]-:** Ship in tightly sealed containers, protected from light and moisture. Use secondary containment and appropriate chemical labels. Transport as a hazardous chemical according to relevant regulations. Ensure compatibility with surrounding cargo, and provide Safety Data Sheet (SDS) during shipping. Handle with gloves and proper personal protective equipment (PPE).
    Storage Store **Phenol, 3,5-Difluoro-4-[5-(1-methylethyl)-1,2,4-oxadiazol-3-yl]-** in a tightly sealed container, away from light, heat, and moisture. Keep in a cool, dry, and well-ventilated area, segregated from incompatible substances like strong oxidizers and bases. Use appropriate safety cabinets for corrosives or organics. Label the storage clearly and ensure access is restricted to trained personnel.
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    Certification & Compliance
    More Introduction

    Phenol, 3,5-Difluoro-4-[5-(1-Methylethyl)-1,2,4-Oxadiazol-3-Yl]-: Insight From the Manufacturer’s Floor

    Real-World Chemistry Shaping Industry Outcomes

    There’s a certain energy you feel on the industrial plant floor—part calculation, part experience, and a fair bit of anticipation for each batch’s progress. Phenol, 3,5-Difluoro-4-[5-(1-Methylethyl)-1,2,4-Oxadiazol-3-Yl]- has earned its place in our chemical lineup, not because it fits into a preconceived standard box, but because our years behind the vessels, pumps, and analyzers show us that specialized molecular frameworks focus scientific work in the right direction. This particular aromatic fluoro-phenol, with its oxadiazole ring, does not play by the rules of basic chemistry. Its synthesis demands clean, stepwise control—every intermediate isolated, every pH checked, and every reaction vessel flushed twice for next-batch reliability. Most importantly, the product coming out of the reactor faces far more scrutiny here than the glossy, vendor-supplied spec sheets might suggest.

    Building a Better Intermediate: Our Day-to-Day Experience

    Years of producing halogenated phenols and heterocyclic intermediates made us wary of shortcuts. There’s a lot of discussion in the trade about purity, but the conversation rarely lands on persistent issues: off-notes in the product, scale-up headaches, or unidentified impurities that show on NMR later. For Phenol, 3,5-Difluoro-4-[5-(1-Methylethyl)-1,2,4-Oxadiazol-3-Yl]-, the work begins with dialed-in distillation. Our reactors carry out the installation of those two fluorines without over-halogenation, which took time to master. The integration of the isopropyl-oxadiazole fragment needs real attention to pH, temperature, and residence time. There’s no way around it: reliable output means taking samples every couple of hours, loading them straight into the HPLC, and being ready with solid troubleshooting routines.

    Monthly batch logs keep us honest. If color drifts even slightly, or GC picks up micro-impurities, nobody pretends it’s “close enough.” Our goal is a material that matches the requirements set out by downstream pharmaceutical, agrochemical, and advanced material developers. They aren’t interested in short-term shipments with hidden baggage. Poor repeatability wrecks pilot targets, especially at kilogram scale; we've seen it firsthand, and work closely with our QA technicians to head off recurring culprits.

    Why the Structure Stands Out

    From a synthetic chemist’s eye, every substituent group shifts the molecule’s core behavior. The difluoro substitution makes the phenolic oxygen less nucleophilic, supporting resistance to oxidative decomposition—a requirement we've run into again and again for intermediates exposed to oxygenation or high-temperature downstream steps. Fluorine's electronegativity protects key bonds and raises thermal stability, properties critical for multi-step production campaigns involving heat and pressure. Regular phenols fall short in these departments; we've run direct comparisons, and the difference in thermal gravimetry analysis backs this up every time.

    The oxadiazole system imparts further utility. More than once, developers from R&D have told us about the headaches of instability in simpler benzenes during their transformations. The oxadiazole moiety by itself brings notable electron delocalization, reducing localized degradation in harsh reaction environments, especially useful in active ingredient synthesis. Adding isopropyl on that ring can modulate lipophilicity, a small change with big consequences. We learned this when trialing customer-supplied protocols intended to increase cell penetration in pharmaceutical exploration or enhance substrate compatibility for surface science.

    Quality Consistency: How We Approach Each Batch

    Production-scale chemistry runs up against a hard wall: minuscule changes become major issues at larger volumes. The more complex the molecule, the less tolerance there is for improvisation. We document each part of the crystallization, transfer lines thoroughly checked to ward off memory effects from earlier runs, and we habitually double-filter solids—no apologies for the extra effort or loss in yield, because months of QC investigations have proven that even minor filtration changes can influence solid-state form and solubility. Our technicians work with glassware as well as reactors, keeping a small parallel batch bench-checked before any full run is cleared.

    It’s tempting for some in the industry to accept just-in-time analytics and rely on basic melting point and HPLC. Years spent debugging small off-white spots, slight endothermic dips, and “vague” impurity peaks make us rely more on long-form NMR, FTIR mapping, as well as secondary tests aligning with customer application feedback. Outcomes matter more than quick passes. We scrutinize every result across consecutive lots, ring the changes when our data starts to drift, and we have pulled shipments when out-of-trend lots cannot be explained at the bench.

    Specifications That Matter in Practice

    The key criteria for Phenol, 3,5-Difluoro-4-[5-(1-Methylethyl)-1,2,4-Oxadiazol-3-Yl]- go far beyond nominal assay and appearance. Our material typically achieves a purity above 99.3% by HPLC, but by itself, that number isn't the end-goal. What counts is absence of persistent minor impurities—those low-ppm ghosts that hide in poorly rinsed or aged equipment. Moisture and residual solvents, if undetected, sabotage both reactivity and shelf stability. Every time we cross-analyze for class 1 and 2 solvents, and after a few incidents early in our scale-up history, we started including more rigorous residual moisture checks. A typical melting point lands in the narrow 110–112°C range, and every lot report gets a cross-run against the internal reference spectrum.

    Different industries each have their own pain points—pharma needs predictable reactivity and impurity control; leading electronics groups have zero tolerance for batch-to-batch variation in physical parameters. We know our customer’s reality, not just from phone calls but from years of working with R&D teams to customize purification or drying, and chasing down root causes when yields dip below specification.

    How Usage Issues Surface: The Human Side of Scale-Up

    Most industry commentary skips over the rough spots faced during tech transfer and formulation. On the real production side, introducing a molecule like this into a downstream process doesn’t happen in a vacuum. Variable solubility profiles—and the way solvents or co-solvents interact—change the entire processing logic. This fluoro-oxadiazole structure responds best in select polar aprotic solvents; years of trial have shown risks if agility in solvent strategy is missed, either at pilot or kilo scale. We've had partners relay stories of expensive retooling after preliminary screenings missed unique solvation or unexpected salt formation. Knowledge gained from shared troubleshooting led us to adjust our drying and packaging protocols and stop new solvent blends from slowly contaminating end-user pipelines.

    In real-world labs, this compound’s modest volatility makes strict storage a must, as trace air oxidation can creep in over time and degrade product. We learned, sometimes the hard way, that silica gel packs and nitrogen sealing guard stability better than simple amber glass. Consistent particle sizing also saves headaches for automated handling in higher-volume applications. Whenever possible, we talk directly with the chemists and engineers handling the next step, offering firsthand observations on any tendencies for clumping, electrostatic build-up, or unforeseen reactivity with metal process pipes.

    The Competitive Angle: How This Intermediate Sets Itself Apart

    Comparisons to standard difluorophenols, or even related oxadiazole phenols, turn up key distinctions—differences that matter out on the production floor or in a real analytical suite. The presence of the isopropyl group on the oxadiazole makes for a unique solubility fingerprint and alters the molecule’s reactivity profile, especially important for those pursuing application in medicinal chemistry where final-column purification steps can become bottlenecks. Our direct synthesis route eliminates both the risk of chlorinated byproduct carryover and the rare but persistent “tail” fractions that haunt extended colonnade purifications.

    We’ve run side-by-side batch trials with both basic difluorophenol and this oxadiazole derivative. There’s a stark difference in chemical stability, with this structure holding up under harsher conditions without yellowing or forming side oils. Application feedback from our customers pointed us to new use cases—compounds once written off as too unstable for multi-step drug discovery now stay viable. Agricultural formulation teams reported lower levels of unstable breakdown products and less influence from minor temperature excursions in storage, thanks to a robust oxadiazole backbone handling light and humidity variations.

    How Manufacturing Decisions Protect Quality Downstream

    Every piece of process control, from how we meter the fluorinating agents to fine-tuning drying cycles, helps the final user’s success. It’s easy to overlook the equipment cleaning, but one unscheduled “memory” residue from an earlier batch shows up months later as a failed scale-up or delayed analytical pass. We schedule routine cleaning validation, baseline checks of reactor glassware integrity, and full line purging. Documentation does more than tick regulatory boxes; it’s living proof that errors cost more than time—they damage trust and the reputation built with every reliable delivery.

    One forgotten step—a skipped pH check before coupling the oxadiazole fragment—led to the discovery that even minor deviation can generate a stubborn isomeric impurity. These kinds of learning moments get passed around our shift handoff meetings, posted at the production board, and factored into our updated protocols.

    Environmental Impact and Responsible Production

    Handling halogenated aromatics and oxadiazole rings creates unavoidable environmental risk points. At our site, solvent recovery systems run full-time, and we operate secondary containment around all storage vessels handling fluoro-containing intermediates. Spent reactants undergo multi-step neutralization to avoid trace fluorine pollution. Recycling solvents translates to both a direct cut in input materials and clear reductions in hazardous waste. Our staff reviews these figures not just for reporting, but as a day-to-day measure of process safety. Monitoring actual solvent loss, not just theoretical yield, forms part of our internal review. After a few high-profile regulatory incidents in the industry, the learning was clear—continuous improvement and investment in green chemistry are not just regulatory expectations, but protect long-term viability in global supply chains.

    Our plant tracks every significant waste stream in real time, logging spills or off-spec waste generations. Recovery rates and atmospheric controls deliver both a cleaner working environment and reliable, compliance-backed supply to our partners. We have a direct stake in limiting batch failures—not only for cost control but because persistent environmental issues can close markets overnight.

    Collaborative Problem Solving: Stories From the Plant Floor

    Every seasoned shift supervisor knows the pressure of hitting tight delivery schedules while dealing with chemistry that sometimes fights back. In the story of this compound, both new and experienced team members found themselves troubleshooting a recurring trace impurity. It took re-tracing the synthetic pathway, double-checking upstream reagent sources, and running live side-by-sides on smaller reactors. The breakthrough came when a junior chemist caught the lower purity of a common starting material that passed basic tests but failed more sensitive methods. It’s the sort of team-driven discovery that keeps a manufacturer honest and pushes standards higher. No outsourced consultant, spec sheet, or distant QA department threw the switch; it was a hands-on process culture sharpened by lessons learned batch after batch.

    Over the years, direct collaboration with downstream users taught us that application issues rarely track to a single variable. Researchers reporting sluggish reaction rates in drug candidate synthesis, or instability in advanced coatings, sent us back to our own analytics and, sometimes, to reformulate part of our process—from refining crystallization points to changing reagent suppliers. The compounds arriving at their doorsteps are only as good as the communication that flows in both directions. That feedback loop tightens the chain, leading to superior results whether it’s for a pharma intermediate, an active in next-generation surface science, or a lead compound in agricultural research.

    End-Use Experiences: Why Our Approach Pays Off

    Real-world results speak louder than claims. One pharmaceutical developer saw a consistent 8% yield improvement across several runs by swapping out a competing difluorophenol. They traced the gain to better stability under prolonged reflux. Another advanced material client highlighted the compound’s consistent granule size, which cut losses during a notoriously messy transfer step. Agricultural chemistry partners reported fewer downstream hydrolysis products, easing the regulatory registration process for a new field treatment.

    Each day in production pushes us to ask tough questions: Where are we missing traces? What’s the next impurity that could dull application success? We’ve passed up the chance to cut corners at key points—choosing extra purification, giving up on certain fast but dirty methods, and running longer drying cycles that cost us cycle time but protect final product stability.

    Examining the Marketplace and Future Prospects

    Demand for high-performance intermediates won’t slow. With Phenol, 3,5-Difluoro-4-[5-(1-Methylethyl)-1,2,4-Oxadiazol-3-Yl]-, forward-looking teams are aiming at higher-drug potencies, smarter surface treatments, and more resilient agrochemical actives. The performance and processing benefits showed up repeatedly as key purchase drivers. The value of closely monitored process controls—beyond simple spec adherence—forms the gap separating top-quality outputs from also-rans. Manufacturing the real article, day in and day out, sets a truth standard built by evidence. Each producer’s lived history, technical problem-solving, and ability to scale up without erosion in quality matters more than price in critical industries.

    Where other related products drift off-spec if a minor parameter changes, our strict batch discipline and production traceability become a foundation that customers build on, not a gamble. Future prospects rely on the proven record of many kilograms shipped, dozens of site audits, and ongoing, two-way laboratory trials with our demanding downstream partners. Whether adapting to stricter environmental rules, substituting obsolete reagents, or onboarding new automation for analytics, our plant continues to evolve as chemistry gets smarter and demands climb ever higher.

    Closing Reflections: The Manufacturer’s Commitment

    As both the producer and the problem-solver, our team views each kilogram of this compound not as a line item, but as a project—with history, lessons, and the stakes of hundreds of subsequent syntheses riding on it. Getting the process right once matters less than hitting bullseye each cycle. Customers and their chemists see the impact in their daily work, in fewer unexpected side reactions, higher yields, and reliable documentation when reviewing their processes. Our commitment aligns with theirs, grounded in transparent processes, fast communication, and a willingness to assume responsibility beyond the plant’s gate.

    The manufacturing community achieves results not from hollow claims, but from proven science and the lived testimony of quality over expedience. For those reaching for breakthroughs in chemicals, pharmaceuticals, or advanced materials, Phenol, 3,5-Difluoro-4-[5-(1-Methylethyl)-1,2,4-Oxadiazol-3-Yl]- stands as the result of hard-won efficiency, process mastery, and unwavering attention to the real demands of chemical production and application. We continue to invest in this reality—and work alongside our customers to ensure each challenge is met with both skill and principled care, batch after batch.