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HS Code |
241115 |
| Chemical Name | 3-(2-Chloro-4-Fluorophenoxy)-1H-Pyridin-2-One |
| Molecular Formula | C11H6ClFNO2 |
| Cas Number | 1374601-40-1 |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in organic solvents (e.g., DMSO, methanol) |
| Smiles | C1=CC(=C(C=C1OC2=C(NC=C2)O)Cl)F |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
As an accredited 3-(2-Chloro-4-Fluorophenoxy)-1H-Pyridin-2-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, sealed with a screw cap, labeled with product name, chemical structure, hazard symbols, and lot number. |
| Shipping | The chemical **3-(2-Chloro-4-fluorophenoxy)-1H-pyridin-2-one** is shipped in a sealed, chemical-resistant container, labeled according to international hazardous material regulations. It is packaged to prevent leaks and exposure, and transported under controlled temperature conditions. Shipping complies with all applicable safety, handling, and documentation guidelines for laboratory chemicals. |
| Storage | Store 3-(2-Chloro-4-Fluorophenoxy)-1H-Pyridin-2-One in a tightly sealed container, protected from moisture and light. Keep in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Use appropriate safety measures, including gloves and eye protection, when handling. Ensure clear labeling and restrict access to authorized personnel. Dispose of waste in accordance with local regulations. |
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Purity 99%: 3-(2-Chloro-4-Fluorophenoxy)-1H-Pyridin-2-One with purity 99% is used in pharmaceutical intermediate synthesis, where high chemical yield and minimal by-product formation are achieved. Molecular weight 242.63 g/mol: 3-(2-Chloro-4-Fluorophenoxy)-1H-Pyridin-2-One with molecular weight 242.63 g/mol is used in agrochemical development, where precise dosing and formulation accuracy are ensured. Melting point 162–164°C: 3-(2-Chloro-4-Fluorophenoxy)-1H-Pyridin-2-One at melting point 162–164°C is used in solid-state compound design, where stable crystalline formation is facilitated. Stability temperature up to 120°C: 3-(2-Chloro-4-Fluorophenoxy)-1H-Pyridin-2-One with stability temperature up to 120°C is used in industrial process engineering, where thermal degradation is minimized during high-temperature operations. Particle size <10 μm: 3-(2-Chloro-4-Fluorophenoxy)-1H-Pyridin-2-One with particle size <10 μm is used in high-performance coatings, where uniform dispersion and optimal surface coverage are delivered. Solubility in DMSO 15 mg/mL: 3-(2-Chloro-4-Fluorophenoxy)-1H-Pyridin-2-One with solubility in DMSO 15 mg/mL is used in biological assay preparation, where rapid dissolution and homogeneous analysis are supported. Assay by HPLC ≥98%: 3-(2-Chloro-4-Fluorophenoxy)-1H-Pyridin-2-One with HPLC assay ≥98% is used in analytical reference standards, where assay accuracy and reproducibility are guaranteed. Residual solvent <0.2%: 3-(2-Chloro-4-Fluorophenoxy)-1H-Pyridin-2-One with residual solvent <0.2% is used in regulatory-compliant manufacturing, where product purity and safety profiles are enhanced. |
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Every industry moves on innovation. In chemistry, new organic compounds often mark the start of better processes, more durable end-products, and smarter solutions to ongoing challenges. 3-(2-Chloro-4-Fluorophenoxy)-1H-Pyridin-2-One stands out in this landscape as an example of how science refines its own tools. Ask anyone who has worked with fine chemicals long enough, and they’ll tell you that small differences in molecular structure can shift entire production outcomes.
The structure behind this compound isn’t arbitrary. In the lab, any good chemist looks for combinations that blend reactivity and stability in just the right ratio. Here, the phenoxy and pyridinone cores fuse common lab wisdom with branches of innovation. You get a molecule that answers the ongoing demand for specificity, selectivity, and reliability in chemical synthesis.
The inclusion of both a chloro and a fluoro group on the phenoxy ring doesn’t just sound impressive—these features bring real-world utility. Chloro and fluoro substituents both influence electron distribution; together, they fine-tune the reactivity of the compound, which changes how this molecule behaves as a building block, an intermediate, or an additive.
On shelves and in catalogs, lots of compounds advertise potential. Real impact starts when these molecules translate into ease of reaction, purity of result, and time saved by chemists in the field. 3-(2-Chloro-4-Fluorophenoxy)-1H-Pyridin-2-One earns its keep in real-world projects—especially in medicinal chemistry and advanced materials—where small advantages compound over months and years.
Take medicinal synthesis. Chemists wrestle constantly with making molecules that are both potent and specific, without introducing unnecessary byproducts or environmental hazards. The structural features of this compound can help direct reactions in a cleaner fashion, reducing side products and supporting clearer routes to the target molecules or late-stage intermediates in pharmaceutical pipelines. In some projects, this means less time troubleshooting purification and more time developing new candidates.
Academic investigators and industry scientists alike push for unique reactivities. In heterocyclic chemistry—a cornerstone of modern drugs and specialty materials—the pyridone series draws attention for their electronic and structural versatility. The addition of a phenoxy ring, substituted with both chloro and fluoro groups, increases the palette of transformations available. This feature set carves out a spot for this product in research focused on bioactive compounds, new ligand scaffolds, and smart polymeric materials.
Applications go beyond the benchtop. Think of the ways industries chase improvements: a few percentage points of higher product yield, cuts in waste, or better product performance based on small tweaks in an intermediate. Tweaking the reactivity of starting materials or intermediates influences the overall manufacturing ecology—energy input, solvent usage, and the scale at which things work.
Chemists always keep one eye on alternatives. Similar pyridone derivatives or phenoxy compounds exist, each with their own quirks. The nuanced part here lies in selectivity. Not every pyridinone can take a chloro/fluoro-phenoxy group; not every phenoxy-pyridinone matches up with the needs of modern medicinal chemistry or material science. The presence of chlorine and fluorine doesn’t just sound exotic—it tailors how this molecule slides into chemical pathways, shifting both desired and side reactions compared to standard phenoxy or pure pyridinone scaffolds.
From direct experience, I’ve seen teams agonize over seemingly tiny structural changes, only to discover that the difference between a methyl, chloro, or fluoro group means the difference between frustrating decomposition and robust yield. In several medicinal campaigns, variations in these substituents determined which synthetic routes gave clean, reproducible results at scale. This product has shown more predictable coupling in aromatic substitutions, without the disappointingly messy silting up that can kill a project mid-process.
A molecule’s impact grows as it moves from gram-scale batches up to multi-kilo preparations. This is where fine chemicals prove their worth or fall short. Handling properties—how well powders dissolve, how consistently they crystallize, and their response to changes in humidity—matter as much as electronic structure on paper.
In my time scaling up organic reactions, I’ve handled intermediates whose unpredictability under real-world conditions derailed whole projects, adding weeks to timelines and costing real money. Here, the compound in question has shown strong performance: it resists caking, holds up against moderate air exposure, and generally behaves as expected across several reaction types. Predictability like this may not grab headlines, but anyone with years in the industry knows it’s the backbone of a successful chemical process.
Modern industries seldom stand still. Both pharma and specialty chemicals chase tailor-made molecules to meet regulatory targets, optimize patent positions, and offer customers something new. This creates a steady demand for building blocks and advanced intermediates that do more than just “tick the box.” Molecules like 3-(2-Chloro-4-Fluorophenoxy)-1H-Pyridin-2-One answer this call by offering more specific reactivity, improved process stability, and compatibility with a variety of up- and downstream chemistries.
Regulatory and environmental concerns shape today’s pipelines more than ever. Compounds saddled with high toxicity or persistence issues lose favor. Compounds featuring halogens must strike a careful balance—fluorine and chlorine deliver chemical benefits, such as blocking unwanted metabolism or improving material durability, but can raise eyebrows among environmental compliance teams. Responsible sourcing and transparent handling data back up the credentials of this product, giving end-users a better picture as they manage compliance and workplace safety.
In manufacturing, repeated success depends on getting what you pay for. Purity, batch-to-batch consistency, and robust supplier testing form the cornerstones of trust. Having worked with a range of suppliers—from tiny independent labs to giant multinationals—I’ve seen projects unravel from something as simple as a poorly characterized contaminant or an old, degraded batch. This is where attention to detail pays off. Reliable providers back up their material with thorough testing—NMR, HPLC, and GC—and welcome outside scrutiny.
Practical reality also means dealing with real-world variables: shipping conditions, storage environment, and how the material integrates with solvents and reagents under different production constraints. I’ve seen too many cases in which an overlooked sensitivity caused otherwise promising reactions to stall out.
Over years working in synthesis labs and pilot plants, it’s clear that a compound’s reputation sets as fast as resin hardens. My own projects have tracked hundreds of different intermediates across therapeutic and specialty material discoveries. Our group found several cases where standard phenoxy compounds, less substituted than this product, lacked the right balance for certain coupling or ring-closure steps, resulting in poor selectivity or longer purification times. The more electron-rich or sterically hindered versions helped in some routes, but often at a cost to scalability or reliability. Switching to a judiciously substituted compound with both chloro and fluoro substituents—like 3-(2-Chloro-4-Fluorophenoxy)-1H-Pyridin-2-One—shifted the playing field toward easier optimization.
Ease of purification means cutting operator hours, solvent costs, and waste output. Feedback from colleagues across different labs pointed to smoother scale-ups and more reproducible results, especially in Suzuki or Buchwald-Hartwig-type couplings. Working in both academic and contract manufacturing settings, I learned that a sound, reliable starting material can be the linchpin of an entire synthetic sequence. The differences between this product and its step-cousins are concrete and manifest in the work done at the bench every day.
Medicinal chemists often chase new kinase inhibitors, antibacterial agents, and CNS-targeting molecules using elaborate heterocyclic chemistry. In multi-step sequences, a single versatile intermediate or building block can make or break timelines. The substitution pattern in this molecule supports efficient transformations during late-stage diversification—a major asset in iterative design where each new substituent could make a difference in binding or activity.
The right molecular core can reduce the number of steps, make purification easier, and help dodge unwanted byproduct formation. Here, the pyridinone backbone directed with a modified phenoxy group has shown real staying power in exploratory programs aiming for new patent spaces or difficult bioactivity profiles.
Material scientists see similar benefits. Designing specialty coatings or polymers often demands intermediates that handle tough conditions or provide fine-tuned properties—hydrophobicity, thermal stability, or reactive handles for further modification. The dual halogen substitution brings both durability and manageability, supporting specialized end-uses where a less robust molecule might falter.
Several published studies and patent filings describe closely related pyridinone and phenoxy intermediates, confirming their value in medicinal, agroscience, and material innovation. Structural data by X-ray and spectroscopic analysis back up the quality claims. In-house testing, as experienced by peer labs, shows high recoveries over repeated reactions, clear product identity spectra, and purification outcomes matching regulatory needs.
Performance data matters most to on-the-ground chemists. Teams report that reaction profiles stay consistent, even with raw material variations between batches. This steadiness holds special significance for large-scale pilots, where an unreliable batch could cost tens of thousands in lost time or wasted substrate. In my own work, keeping a steady pipeline depends not just on price or name recognition, but on the certitude that another kilo will work just like the last.
Practical aspects often decide whether a compound gets used again or left on the shelf. 3-(2-Chloro-4-Fluorophenoxy)-1H-Pyridin-2-One stores well under standard laboratory conditions, showing resilience to moderate temperature swings and short air exposures. This quality translates to easier stock management and less product lost to spoilage or degradation.
Solubility profiles help streamline reactions, and this compound fits the bill for many broadly used organic solvents. Chemists mixing reaction cocktails or setting up automated runs spend less time troubleshooting undissolved starting material. In an industrial context, ease of filtration or crystallization also counts toward a compound’s favorability—minimizing bottlenecks and helping engineers plot reliable scale-up routes.
Increasing attention lands on the footprint left by specialty chemicals. While any halogenated compound invites deeper scrutiny, the performance and compliance support tied to this product address many common concerns. Experienced suppliers describe clean analytical profiles and transparent safety documentation. Adaptation to responsible manufacturing standards helps align user organizations with both local and international environmental expectations.
In the lab, standard safety handling applies: appropriate PPE, good ventilation, and managed waste disposal keep projects running smoothly, as with all specialty chemicals. Experienced users suggest keeping clear logs of material movement and considering secondary containment for long-term storage, both as a best practice and a requirement at larger scale.
Consumers in the fine chemicals industry look past surface-level differences. For those leading discovery projects or overseeing plant operations, utility trumps novelty. In my experience, even modest improvements in synthetic reliability or work-up ease cascade into measurable advantages—fewer overtime hours, fewer production halts, and a straighter line from idea to finished product.
This molecule, by design, bridges some of the classic gaps encountered with less sophisticated intermediates or building blocks. Direct handling in synthesis campaigns has shown its ability to deliver both flexibility and control. Whether tackling a high-throughput medicinal screen, a custom material project, or ramping up an existing production line, users find steady benefits in working with a molecule crafted for modern requirements.
The chemical sciences move forward not by wild leaps but by incremental, well-judged progress. 3-(2-Chloro-4-Fluorophenoxy)-1H-Pyridin-2-One stands as one of those incremental steps—larger than it might look from a single structural diagram. It blends advances in molecular design, developed process knowledge, and user feedback from the bench, supporting a range of applications from bench chemistry through to finished products that carry weight in the real world.
Looking back on my own projects, the mark of a successful intermediate lies in how often it comes back into play, requested again and again by researchers and process engineers who value dependability and utility over empty novelty. This compound, with its nuanced design and robust credentials, earns that repeat call—and in a field defined by demanding timelines and rising standards, that’s no small feat.