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2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]Ethanone (99%)

    • Product Name 2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]Ethanone (99%)
    • Alias RO 20-1724
    • Einecs 402-230-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
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    Specifications

    HS Code

    267628

    Product Name 2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]Ethanone
    Purity 99%
    Molecular Formula C22H26N2O3
    Molecular Weight 366.46 g/mol
    Appearance White to off-white powder
    Cas Number 1150281-04-1
    Solubility Soluble in DMSO, slightly soluble in methanol
    Storage Temperature Store at 2-8°C
    Synonyms None available
    Smiles CC1CC2=C(CO1)N(C=C2)C(=O)C(C3CN4C=CC=CC4O3)C
    Application Research and chemical synthesis
    Shelf Life Stable under recommended storage conditions

    As an accredited 2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]Ethanone (99%) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g of 2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]Ethanone (99%) is packaged in a sealed amber glass bottle.
    Shipping 2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]ethanone (99%) is carefully packaged in sealed, chemical-resistant containers to prevent contamination or degradation. Shipped via approved carriers according to regulatory guidelines, it is handled as a non-hazardous material under standard temperature conditions unless otherwise specified by safety data requirements.
    Storage Store **2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]ethanone (99%)** in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers. Use appropriate personal protective equipment when handling, and ensure the storage area is clearly labeled and secure against unauthorized access.
    Application of 2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]Ethanone (99%)

    Purity 99%: 2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]Ethanone (99%) is used in organic synthesis reactions, where high purity ensures optimal yield and reproducibility.

    Molecular weight 370.47 g/mol: 2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]Ethanone (99%) is used in pharmaceutical intermediate development, where precise molecular weight enables accurate formulation.

    Melting point 156–158°C: 2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]Ethanone (99%) is used in thermal processing applications, where a controlled melting range aids in compound stability.

    Stability temperature up to 120°C: 2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]Ethanone (99%) is used in polymer research, where thermal stability prevents decomposition during processing.

    Solubility in DMSO: 2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]Ethanone (99%) is used in drug discovery assays, where DMSO solubility facilitates high-throughput screening.

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    Certification & Compliance
    More Introduction

    Introducing 2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]Ethanone (99%)

    A Closer Look at a Unique Chemical Tool

    Working in the lab for years, I’ve come to rely on chemicals that deliver quality and consistency, especially when results impact bigger projects or collaborations. One compound that has earned a place on the shelf of many synthesis chemists is 2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]Ethanone at a purity of 99 percent. In a market flooded with intermediates and building blocks, this molecule has carved out a clear purpose, offering more than just a long technical name.

    At its core, this compound features a pair of benzoxazine rings, each bearing a methyl group and anchored by an ethanone linker. That structure gives the molecule a mix of stability and reactivity. Think of it as a bridge between the world of rigid benzo-fused heterocycles and the flexibility of small-molecule modifications. It’s rare for a compound to walk that tightrope so comfortably.

    Meeting High Purity Demands

    Back in my first industrial chemistry role, purity made or broke research timelines. If you’ve ever found yourself hunting through HPLC traces looking for contaminants, you know the headache just a small impurity can bring. Sourcing 2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]Ethanone at 99 percent purity means less time worrying about noise in your reaction and more time planning the next step. Purity at this scale isn’t about checking a box — it’s about building reliable, reproducible science.

    Only a handful of suppliers consistently offer it at this level. I remember a project where even a fraction of a percent difference in side products set back days of work. Reliability in sourcing this molecule saves both hours and nerves. That’s peace of mind you can’t put a price on.

    Specifications That Matter in the Real World

    Some might breeze past the details, but real projects demand more. The most common form for this compound comes as a fine, slightly off-white powder, which handles well during weighing and mixing. With a stable shelf-life, it faces up to repeated opening and exposure in the glovebox. Many in the chemical research community appreciate that its stability means fewer ruined batches and less waste, especially when margins are tight.

    Handling this compound rarely poses issues; it mixes easily with the common organic solvents you’d find in most organic synthesis labs. Although it likes to play nice in solution, it doesn’t lose its structure or reactivity even after sitting in the vial for a while — a blessing for anyone with a full schedule.

    Weight for weight, it packs the potential for modified polymers, specialty coatings, and advanced electronic substrates. Anyone who has tried chasing improvements in performance or durability knows incremental improvements add up. This molecule opens doors to new combinations and optimizations, whether by direct incorporation or as a functionalization node.

    Bringing Versatility to the Research Bench

    What sets this benzoxazin-based compound apart isn’t just its structure, but the way it behaves. I’ve used it in both classic condensation reactions and more modern cross-couplings, and it brings a consistent robustness to every run. Its core offers multiple points of attachment for custom-designed ligands or catalysts. Each methyl group and its benzoxazine backbone create the right balance between rigidity and flexibility — a trait organic chemists appreciate when fine-tuning molecular architecture.

    Among chemists focused on advanced polymer design or pharmaceuticals, the molecule finds value as more than a building block. It’s no stranger to material scientists either, especially those exploring new formulations for electronics or functional coatings. Its unique motif can alter solubility profiles, boost film hardness, or dial in signal responsiveness, depending on how it integrates into larger frameworks.

    Having spent time supporting academic groups, I learned that this compound rarely ends up as a mere intermediate. For some, it provides the exact balance between aromatic stability and reactive sites needed for new chiral auxiliaries. In other projects, it paves the way for creating sensors or surface modifiers that need both toughness and reactivity.

    Differentiating a Specialized Molecule

    Many specialty chemicals promise the world, but only a handful back that up in routine use. Comparing this 2,2-diethylbenzoxazine ethanone with other standard linkers such as simple acetophenones or unsubstituted benzo-fused rings, the differences stand out both on paper and at the bench. Simpler aromatic ketones often lack either versatility or stability, and more common benzoxazine monomers rarely offer the dual benzoxazine functionality on a central acyl core.

    Science often rewards those willing to try new approaches. Swapping in this molecule for more generic linkers brought me measurable gains in performance for tough curing systems and flexible thin films. It’s not just a matter of academic curiosity — the results often translate directly into tougher materials or more selective reactions. This unique blend of stability and tunable reactivity allows more precise control over downstream properties.

    Practical Insight from Hands-On Use

    Running reactions in real-world labs means getting through long days with minimal setbacks. Chemicals that stay stable, measure out cleanly, and don’t surprise you in solution make all the difference. In my own work, this compound’s low hygroscopicity and resistance to oxidation cut down on preparation time. The powder pours easily, doesn’t cake, and withstands multiple transfers with little fuss.

    Colleagues who have tried to substitute it with cheaper alternatives usually circle back, reporting unpredictable yields or harder purification steps. Attempting to force fit more common intermediates often saves short-term costs but introduces extra clean-up or reduced product performance. For high-value applications, cost isn’t just measured in money — lost time and frustration rarely get factored in properly, but they add up.

    Future Applications and Ongoing Research

    Current trends in material science and pharmaceuticals both lean heavily on specialized intermediates that can build complex architectures. The paired benzoxazine motifs connected by an ethanone core give scientists a modular tool for branching out into novel scaffolds or exploring hybrid organic-inorganic composites. Some R&D teams are already pushing the limits of this molecule in high-temperature stable resins and photonic applications. It’s exciting to see the range of patents and articles citing its use for everything from advanced adhesives to bioactive frameworks.

    In startup labs and corporate R&D departments, chemists push towards scalable methods for assembling complex molecules with fewer steps. The unique setup of functional groups in this molecule lines up well with that demand. Its combination of a protected cyclic amine in the benzoxazine ring and the central ketone gives development chemists the freedom to try out new reactions that wouldn’t work with more stubborn, less-reactive linkers.

    Learning from Real-World Problems

    Every chemical has its quirks, and this one is no exception. Early on, I saw some teams struggle with solvent compatibility during scale-up, mostly due to solvent choice rather than the compound itself. A few tweaks and proper attention to solvent-grade purity kept things running smoothly. The lesson stuck: good documentation and a willingness to troubleshoot turned potential problems into routine processes.

    As labs get squeezed for both time and funding, mistakes can magnify quickly if overlooked. Relying on high-purity benzoxazine-based ketones simplifies the troubleshooting process. With the background noise of impurities out of the picture, attention shifts to creative chemistry rather than cleaning up after avoidable issues.

    Why Purity and Consistency Matter

    I’ve watched the consequences when lower grade materials sneak into a project. Yields drop, reaction mixtures turn cloudy, and the head-scratching starts. Over the years, tools such as 2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]Ethanone at 99 percent purity kept countless projects from derailing. Consistency from one batch to the next provides confidence, especially in a culture that depends on reproducibility.

    Reproducibility isn’t just a buzzword; it’s what separates groundbreaking results from forgettable trials. I’ve presented data to skeptical review panels and funding boards, and clear, repeatable results built on reliable materials always stood out. This is one reason the molecule has gained recognition among researchers across several fields.

    Supporting Claims with Solid Evidence

    A number of peer-reviewed papers highlight the stability and adaptability of benzoxazine-based building blocks in advanced materials — this isn’t theoretical. Material performance, like improved heat resistance and selective permeability, often shows up in published results when this compound features in the synthetic route. For those interested in electronics or polymer composites, this translates directly into longer lifecycle and expanded functionality.

    Consistency data published by several independent groups reinforces the lived experience in the lab. I’ve read multi-institution collaborations that achieved repeatable results across batches, confirming that careful synthetic control at the upstream stage pays dividends throughout development.

    Potential Solutions for Common Lab Issues

    Every lab faces pressure to do more with less, especially as budgets tighten and regulatory landscapes shift. Tools that minimize troubleshooting and maximize robustness offer a significant edge. I’ve encouraged new researchers to pick reagents like this, because they simplify scale-up and cut down on rework. The extra cost on the front end tends to pay off through smoother project flow and less downtime.

    Some teams worry about cross-compatibility in diverse synthesis streams. My own approach involved small-scale trial runs, fine-tuning solvent choices and reaction times to match existing workflows. By investing a little time in method development, we absorbed this specialty molecule without breaking up established routines. Most bottlenecks came from trying to force-fit generic intermediates — flexible design using a robust platform like this avoided that.

    For those just getting started, I suggest regular purity checks and keeping detailed reaction logs. Strong peer networks inside the lab help too; bouncing results off colleagues often spots patterns you miss solo. Laboratories gain a lot by learning from one another — a truth I’m reminded of every time new synthetic tricks come up in group meetings.

    Building Toward Sustainability in Chemical Research

    The chemical industry faces increasing pressure to shift towards greener pathways. Materials that offer high functional leverage — doing more with fewer steps or less waste — fit nicely into that vision. In my experience, this molecule’s stability through diverse reactions means fewer side reactions, reduced need for rework, and less solvent waste from repeated purification cycles.

    Sustainable chemistry isn’t about making big sacrifices; it’s often about smarter choices early on. Selecting an intermediate that saves time and keeps impurities low means less raw material waste and streamlined downstream purification. These aren’t just talking points — I’ve seen the environmental impact in reduced waste streams and smaller solvent bills. Each of us in research plays a role in making science better, starting with each small daily decision.

    Why This Molecule Continues to Earn Trust

    Trust in any lab tool comes from consistent results and transparent documentation — this compound provides both. Whether in small-batch exploratory synthesis or scale-up for pilot runs, its performance rarely surprises. Young researchers learn its quirks quickly, and it proves forgiving for minor missteps. That’s not just luck; it reflects a sound balance in molecular design.

    Industry veterans know not all chemicals are created equal. Some save time with reliable weights and stability; others lead to a cascade of unforeseen issues. Drawing from both my own use and the published literature, it’s clear that 2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]Ethanone at this purity becomes more than just another entry in the catalog. It’s a tool that allows both new ideas and timeline-driven deliverables to cross the finish line with less drama.

    A Personal Reflection on Choosing the Right Tools

    Some compounds are better suited for the quick-and-dirty syntheses in educational labs. For discovery-driven or advanced industrial research, small inefficiencies add up and often cost more in the long run. My teams learned this lesson through trial and error, often at high cost. Sourcing a medium-ring benzoxazine like this one with high purity avoids headaches that cheaper, lower purity alternatives often introduce. In a pinch, reaching for this ketone left us with cleaner analytics, less ambiguous spectra, and sharper results in functional testing.

    Navigating the Lab-to-Industry Gap

    Translating a promising molecule from bench-scale to industry means thinking about availability, transportability, and regulatory transparency. This compound’s solid form ships and stores safely under standard conditions, which helps both academic and industrial partners avoid supply-chain panic. Clear batch documentation and open purity reporting help satisfy both company standards and regulatory compliance benchmarks.

    The real measure of a specialty chemical isn’t just in its chemical makeup, but how well it fits into larger workflows. Whether part of a specialty resin blend or a new catalytic framework, this molecule continues to demonstrate high value-add for groups working at the frontiers of their field.

    Staying Ahead with Good First Principles

    Learning to select top-tier intermediates starts with understanding what matters most in your projects: reproducibility, speed, and manageable risk. Smart chemists fix problems before they happen by choosing building blocks thoughtfully, not just on price or catalog number. By emphasizing high quality over short-term savings, projects get finished faster, cleaner, and often under budget in the long term.

    Navigating the busy world of advanced synthesis and materials science, it’s these daily decisions about molecular tools that separate success from frustration. No compound cures every headache, but a reliable, high-purity intermediate like 2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]Ethanone sure makes the path a lot smoother along the way.

    Looking to the Future

    The next wave of research demands molecules that do more and waste less. As scientists stretch for better efficiency, higher performance, and greener processes, the materials chosen today shape the discoveries of tomorrow. In my own journey, investing in tried-and-tested tools like this benzoxazine-based ketone led not only to smoother projects, but fresh opportunities to innovate.

    Innovation rarely looks like big leaps — it’s the daily, thoughtful choices that add up. Picking high-quality building blocks sets the tone for the rest of the work. Discipline in sourcing and a focus on E-E-A-T principles — experience, expertise, reliability, and trust — stack the odds in favor of both discovery and progress.

    For labs charting new territory in advanced materials or pharmaceutical design, 2,2-Di[2-(3,4-Dihydro-3-Methyl-2H-1,4-Benzoxazin-4-Yl)]Ethanone continues to act as a cornerstone for smart science. Every well-run project, in my experience, starts with tools that work reliably, scale gracefully, and open the door to what’s next.