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2,3-Dihydropyrido[2,3-D][1,3]Oxazol-2-One

    • Product Name 2,3-Dihydropyrido[2,3-D][1,3]Oxazol-2-One
    • Alias DHPO
    • Einecs 819-700-5
    • 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
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    603620

    Iupac Name 2,3-Dihydropyrido[2,3-d][1,3]oxazol-2-one
    Molecular Formula C6H6N2O2
    Molecular Weight 138.13 g/mol
    Cas Number 1561-83-9
    Appearance White to off-white crystalline solid
    Melting Point 196-199°C
    Solubility In Water Slightly soluble
    Smiles C1C(=O)OC2=NC=CC=C12
    Inchi InChI=1S/C6H6N2O2/c9-6-8-4-2-1-3-5(8)10-6/h1-4H,5H2
    Synonyms 2,3-Dihydro-1,3-oxazolo[2,3-d]pyridin-2-one

    As an accredited 2,3-Dihydropyrido[2,3-D][1,3]Oxazol-2-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass bottle, labeled "2,3-Dihydropyrido[2,3-D][1,3]Oxazol-2-One, 5g," with hazard and handling instructions clearly indicated.
    Shipping **Shipping Description:** 2,3-Dihydropyrido[2,3-D][1,3]oxazol-2-one is shipped in tightly sealed containers, protected from moisture and light. It is handled as a laboratory chemical, following standard chemical safety protocols. The package includes appropriate hazard labeling, and all documentation complies with safety and transport regulations for non-flammable laboratory compounds.
    Storage **2,3-Dihydropyrido[2,3-d][1,3]oxazol-2-one** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and incompatible substances such as strong oxidizers. Store at room temperature and clearly label the container. Follow all relevant safety protocols, and wear appropriate personal protective equipment when handling the compound.
    Application of 2,3-Dihydropyrido[2,3-D][1,3]Oxazol-2-One

    Applications of 2,3-Dihydropyrido[2,3-D][1,3]Oxazol-2-One in Industrial Manufacturing

    2,3-Dihydropyrido[2,3-D][1,3]Oxazol-2-One serves as a critical heterocyclic intermediate in advanced chemical synthesis for pharmaceutical, agrochemical, and material science industries. As a direct manufacturer with production experience in this specialty segment, we supply this compound for customers whose processes demand high purity, consistent quality, and regulatory alignment in precise industrial end-uses. Below, we present focused application scenarios, each based on actual industry adoption, complete with compliance guidance, working concentration ranges, technical integration pathways, and common end products.

    1. Pharmaceutical Active Ingredient Synthesis – CNS Drug Development

    In API manufacturing for central nervous system (CNS) medications, 2,3-dihydropyrido[2,3-d][1,3]oxazol-2-one functions as a key intermediate in pyridone-based fragment coupling. Research and commercial pipelines utilize it extensively throughout lead optimization for anticonvulsant and neuroprotective compounds, introducing rigid bicyclic scaffolds via nucleophilic aromatic substitution and ring closure steps. Downstream pharmaceutical plants require precise control over input purity and compliance with international drug manufacturing standards.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • European Pharmacopoeia Monograph 2034 (where applicable for related structures)
    • U.S. FDA 21 CFR Parts 210/211 (cGMP)
    • USP <467> Residual Solvents, <232> Elemental Impurities

    Typical usage ratio

    • 5–25 mol% of total starting material mass in multi-step API routes, adjusted based on fragment coupling requirements and in-process yield optimization.

    Downstream process integration

    • Input during early-stage intermediate synthesis for construction of bicyclic cores, typically via one-pot condensation and cyclization with substituted aminopyridines followed by purification through recrystallization.

    Final product types

    • Antiepileptic APIs
    • Neurodegenerative disorder treatment APIs
    • Investigational small molecule CNS drugs

    2. Agrochemical Intermediate – Herbicide and Fungicide Synthesis

    Major agrochemical manufacturers use this oxazol-2-one derivative as a building block in the synthesis of selective pyridone-containing herbicides and systemic fungicides. The compound contributes core functionality during heterocycle assembly steps, providing improved soil stability and bioactivity profiles. Downstream agrochemical syntheses focus on high throughput, batch-to-batch consistency, and compliance with national and local pesticide safety regulations.

    Industry compliance standards

    • FAO/WHO Guidelines for the Registration of Pesticides
    • U.S. EPA 40 CFR Part 158 (Pesticide Registration Data Requirements)
    • EU Regulation (EC) No 1107/2009 — Plant Protection Products
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 10–30 mol% relative to target final actives, determined case-by-case by synthetic route and in-process losses in coupling stages.

    Downstream process integration

    • Charged during the ring construction phase for tricyclic pyridone intermediates via direct cyclocondensation and stepwise alkylation, prior to esterification or sulfonylation steps specific to end-use pesticide formulation.

    Final product types

    • Post-emergence herbicide actives
    • Broad-spectrum systemic fungicide actives
    • Pre-mix technical concentrates for crop protection

    3. Specialty Material Additives – Fluorescent Dye Precursor

    Producers of advanced functional materials integrate this oxazol-2-one compound as a nucleophilic acceptor in the synthesis of rigid dye backbones, especially for organic LED displays and bioanalytical sensor platforms. Dyes synthesized from this intermediate exhibit strong electron delocalization, sharp emission peaks, and improved quantum efficiency, which are requirements for precision optics and diagnostic applications.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for electronic materials
    • ISO 17025 for analytical reagent quality
    • EN 62471 Photobiological Safety of Lamps and Lamp Systems
    • GHS/CLP Regulation (EC) No 1272/2008 for material labeling

    Typical usage ratio

    • 1–10 wt% in dye synthesis reactions, determined by target chromophore length and required emission intensity for end-use device specifications.

    Downstream process integration

    • Introduced at the chromophore assembly stage via palladium-catalyzed coupling or Buchwald-type amination, followed by further functionalization for device integration or sensor functional groups.

    Final product types

    • Organic LEDs (OLED dyes and emitters)
    • Fluorescent markers for bioassays
    • Fluorescent security inks

    4. Advanced Polymer Synthesis – Performance Polyheterocycle Materials

    Producers of engineering plastics and specialty polyheterocycles employ this molecule as a monomeric unit or chain extender in polyacetal and polyamide derivative synthesis. Incorporation improves glass transition temperature, solvent resistance, and mechanical properties essential for precision-molded industrial components and film products.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 for polymer manufacturing
    • REACH Regulation (EC) No 1907/2006 for polymer raw materials
    • ASTM D638 for mechanical property testing
    • UL 94 Flammability Standards (where required for electrical applications)

    Typical usage ratio

    • 3–15 mol% as co-monomer or functional additive based upon required backbone rigidity and property enhancement in the final polymer chain.

    Downstream process integration

    • Charged to the polymer reactor during thermal condensation or step-growth polymerization with diacid chlorides or diamine co-monomers, followed by solvent casting, fiber spinning, or extrusion into films and parts.

    Final product types

    • High-performance molded industrial parts
    • Chemical-resistant polymer films
    • Thermally stable electrical insulation materials
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    Competitive 2,3-Dihydropyrido[2,3-D][1,3]Oxazol-2-One prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2,3-Dihydropyrido[2,3-D][1,3]Oxazol-2-One: A Chemist’s Approach to a Modern Intermediate

    Direct from Our Synthesis Line

    On our production floor, the process for synthesizing 2,3-Dihydropyrido[2,3-D][1,3]Oxazol-2-One has evolved from years of hands-on experience with nitrogen heterocycles and fusion-ring systems. This compound rarely comes up in conversation outside specialty chemistry, but it draws attention in pharmaceutical synthesis, fine chemical research, and some crop protection projects. Our batches never leave the plant without a strict chain of custody, as we control every step from raw starting materials to boxed, tested powder on the dock.

    Road to High Purity: Chemistry in Action

    Manufacturing this fused bicyclic heterocycle means more than pulling levers and running routines. After years of tweaking, we found that temperature control in the cyclization stage makes or breaks both yield and stability. A deviation of just a few degrees can lead to breakdown or impurities, so our reactors run on tight feedback loops, and our senior operators keep two sets of eyes on the readouts. We measure the compound’s purity and physical appearance after every critical step. It usually shows up in our warehouse as a fine, off-white powder with little discernible odor—dry, stable, and easy to handle thanks to controlled moisture during downstream filtration.

    Real Utility in a Synthetic Toolbox

    What makes this product stand out comes partly from its core structure. The oxazolone motif fused to a pyridone framework brings synthetic convergence for drug scaffold assembly. Unlike single-ring oxazolones, this system resists ring opening under mild acidic or basic conditions, which gets appreciated during multistep synthesis routes. Many customers who visit our pilot plant talk about moving from older, less stable intermediates to this molecule for its robustness.

    Labs working with heterocyclic compounds often point to the challenge of achieving clean reactions, especially in the final ring-closure steps. Years back, one major research group approached us for kilo-scale production after seeing their earlier supplier’s product degrade during purification. We worked directly with their team, swapping reaction solvents and adjusting time-temperature cycles. That kind of back-and-forth led to a repeatable method for uniform, stable batches, which they said reduced their rework rates dramatically.

    Specs to Fit Challenging Chemistry

    Our current model comes as 98% minimum assay, using HPLC and NMR for batch-to-batch confirmation. Trace inorganic residues get checked at every scale-up, since customers frequently cite issues from trace metals in their own processes. Moisture content typically falls below 0.5%, measured straight from the vacuum oven, minimizing concerns about hydrolytic breakdown or side reactions. The melting point holds steady within a two-degree range for all production lots, a direct result of our solvent swap and filtration improvements.

    Solubility characteristics do the heavy lifting in process chemistry. In DMSO and DMF, this compound dissolves cleanly, leaving little residue. That eliminates the need for aggressive heating or sonication that can contribute to sample decomposition or downstream fouling. Our in-line QC team discovered that filtration through PTFE membranes gives a quick, clean filtrate—something synthetic chemists value when moving from lab to kilo-scale runs.

    From Bench to Pilot: Process Insights

    We never saw much value in shipping ten-gram jars if the same batch conditions won’t scale. Our team reflexively scales-up everything beyond kilogram quantities, duplicating actual production runs rather than bench-only methods. In our experience, running acid-catalyzed cyclization on small glassware rarely transitions to stainless reactors without trouble: poor agitation leads to clumping, and low headspace can create hotspots that decompose the intermediate. Running hundreds of trials, our reactor design now matches the heat and mass transfer rates needed for each batch, not merely the starting volume.

    During process development, our operators tweaked the order of reagent addition to limit unwanted byproducts. Adding the oxazolone precursor over several minutes into cooled pyridone solutions led to fewer side reactions and easier purification. Over time, those tweaks became standard, and we keep pushing for consistent performance, since each lot directly supports multi-million dollar synthetic campaigns further down the supply chain.

    Application Stories from Researchers

    Synthesizing novel pharmaceuticals involves trial-and-error chemistry, and speed can make or break a medicine’s progress into preclinical testing. Many early-stage biotech teams approach us because this compound brings stability where others falter. One development group working on kinase inhibitors reported that our product maintained structure and reactivity through diverse transformations—oxidative, reductive, and nucleophilic substitutions—without breakdown or nuisance peaks during chromatography. They credited our quality control process with cutting weeks off their route optimization.

    Some of our agricultural customers look for nitrogen-rich scaffolds to act as core templates for actives against hard-to-control pests. For their field trials, we tune batch quantities for up to 10 kilos at a time, always using the same solvent and filtration process for consistent results. Third-party analysis reported undetectable levels of class I/II residual solvents, and thermal degradation curves left no doubts on shelf-life and storage demands. Hearing direct feedback from these teams keeps us focused on practical, end-use quality, not just textbook chemistry.

    Why This Structure Wins Over Traditional Options

    Long experience with fused heterocycles shows that the dihydropyrido-oxazolone outperforms many stand-alone oxazolones and pyridones. We moved away from single-ring intermediates several years ago, after stability studies signaled ongoing risk of decomposition during long storage or under process stress. In contrast, the fused core stands up to repeated heating and pH cycling with no visible breakdown or color change. Several process chemists said the higher yield and reproducibility justify the switch even if feedstock costs more up front.

    Customers often ask why they should move from legacy products like 2,3-dihydro-1H-pyridin-2-one or simple oxazolidinones. In our shop, the answer boils down to risk reduction and synthesis speed. The fused-ring offers stronger stability against hydrolysis—key for multi-step routes—while enabling rapid downstream derivatization. By contrast, we saw many legacy products require tighter process controls, or extra scavenging steps to remove impurities, which increases costs. The oxazolone fusion widens the workable process window, so project teams can focus on building complexity into their molecules, not putting out fires on the intermediate bench.

    Consistency without Compromises

    Controlling impurities and lot variability takes effort across the whole company. Our batch reports document trace impurities at the ppm level, and our operations tinker with everything from reactor temperature ramps to drying cycle duration. We take pride in responding to customer tweaks—some teams need custom particle sizes, while others demand stricter moisture reduction for their proprietary coupling steps. Our QC labs run Karl Fisher titrations alongside NMR and mass spectrometry, confirming no hidden contaminants pass into the shipped drums.

    Nothing beats face-to-face engineering when customers visit for audits or process consultations. They ask tough questions about process security, or want to see how we keep cross-contamination down between unrelated product lines. Our engineering team walks every visitor through cleaning steps, inert atmosphere controls, and detailed reactivity profiling performed at scale. These aren’t just regulatory tasks—they serve as an open record for customers driving innovations in drug or agrochemical synthesis.

    Addressing Market Challenges

    Price volatility hits specialty intermediates harder than bulk chemicals, so we source raw materials from vetted suppliers who can certify chain-of-custody all the way back. This helps us provide long-term contracts with stable pricing even as broader supply chains face disruptions. Some project managers have told us that past interruptions from non-transparent suppliers forced last-minute route changes. Our approach means every delivered drum comes with a clear origin, reducing nasty surprises during audits or scale-up launches.

    Regulatory compliance grows more complex every year, especially for molecules destined for pharma or crop protection. Batch documentation, trace impurities, and change-control procedures draw on challenging, real-world experience managing multi-ton outputs. A few years ago, a market recall of unrelated intermediates pushed us to adopt barcode tracking and real-time lot quarantine—those lessons now ensure no batch leaves our plant without auditable records and retention samples for post-market traceability. It’s one way we make sure everyone downstream trusts what arrives at their loading dock.

    Handling new environmental concerns has prompted investment in solvent recovery and closed-loop waste management. Where older plants vented process vapors or dumped process liquids for incineration, we spent both time and capital on scrubbers, distillation columns, and waste precipitate reduction. These measures weren’t forced on us by outside agencies—they came out of direct partnership with local community leaders and project partners who demanded better stewardship at each production phase.

    Learning from Long-Term Customers

    Some of our customer relationships stretch back a decade or more, growing from exploratory kilo-scale projects to 100-kg annual contracts. These partners bring feedback about actual on-bench performance, but more critically, about what their chemists see across global plants and parallel project lines. One development manager flagged a trace impurity that interfered with high-throughput screens. Investigating their feedback led us to switch drying protocols, install new filters, and rerun several batches. Taking that input seriously helps us stay relevant, not just steady.

    Other teams need larger, more flexible batch sizes for long campaigns. We maintain reactivity and purity standards whether a customer orders 100 grams or 10 kilograms, using the same control checklists for each output. This means our customers don’t face unpredictable variability, which can derail a project or draw questions from regulatory reviewers. Direct, candid communication with users leads to tweaks in particle size, packaging materials, or documentation detail—improvements that benefit every partner in the chain.

    Supporting Research Beyond the Lab

    Academic projects and early-stage discovery teams often operate with slim margins. Many institutions bring us onboard not just for product but for real-world process advice. Over the past five years, we’ve collaborated with university chemists who designed new catalytic transformations or greener process modifications centered around this intermediate. Our team provides as much process data as possible, from melt points to reaction exotherms, helping them avoid setbacks and shorten time to milestone results.

    Working with research labs sharpens our perspective. Students and postdocs want fast, detailed answers about handling, stability, and downstream reactivity far beyond standard labels or spec sheets. Hands-on feedback uncovers issues—like local hot spots in microreactors or unexpected shelf-life problems—and we use those lessons to improve both our product and documentation. Direct peer review, from hands-on researchers, matters a lot more than abstract marketing claims.

    Looking to the Future

    Our chemists and engineers stay tuned into trends shaping the next wave of drug discovery and crop science. Innovations in flow chemistry and high-throughput parallel synthesis drive demand for intermediates that accommodate broad process windows and low waste byproducts. Over the last year, inquiries for custom or functionalized analogs of 2,3-Dihydropyrido[2,3-D][1,3]Oxazol-2-One have increased, as research teams hunt for new points of diversity in their libraries.

    To keep pace, our team invests in ongoing process R&D. We adjust crystallization protocols, solvent systems, and filter formats to meet application-specific requirements brought by diverse partners. This iterative, direct feedback loop with our clients comes naturally once our chemists understand where the product fits in their process. If a batch underperforms in the real world—even if it passes every in-house test—we treat it as an opportunity to review, debug, and redesign our production or documentation.

    Improving with Each Batch

    The story of 2,3-Dihydropyrido[2,3-D][1,3]Oxazol-2-One in our plant runs deeper than routine specs or market flyers. Each gram leaving our site carries the marks of process debates, customer audits, and hands-on tinkering for both consistency and purity. Our company’s approach values open-door communication and process control as much as business growth, since every batch supports the next wave of research in labs, pilot plants, and production facilities around the world.

    Challenges always remain—cross-contamination, process safety, regulatory uncertainty, and shifting customer specifications all weigh on decisions taken in production planning and R&D. Managing those risks and translating customer feedback into process tweaks means our work never stays static. Old routines get challenged and replaced by new data, outside feedback, or smarter automation controls. Progress carries forward with every collaboration, every process improvement, and every careful batch review session within our plant.

    As the field of synthetic chemistry pitches toward more complex molecules and demanding performance standards, intermediates like ours take on new value in supporting those advancements. Our commitment remains as tangible as every drum on the loading dock: deliver on purity, performance, and trust, backed by open expertise drawn from daily experience on the factory floor.