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HS Code |
629629 |
| Chemical Name | Phenylisoxazole |
| Molecular Formula | C9H7NO |
| Molecular Weight | 145.16 g/mol |
| Iupac Name | 1-Phenyl-1,2-oxazole |
| Cas Number | 3875-73-6 |
| Appearance | White to off-white solid |
| Melting Point | 43-45°C |
| Boiling Point | 270°C |
| Density | 1.18 g/cm³ |
| Solubility In Water | Insoluble |
| Smiles | c1ccc(cc1)c2onc2 |
| Pubchem Cid | 3063247 |
As an accredited Phenylisoxazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Phenylisoxazole, 25g, is packaged in an amber glass bottle with a secure screw cap, labeled with chemical name, purity, and hazard warnings. |
| Shipping | Phenylisoxazole is shipped in tightly sealed containers to prevent moisture and contamination. It should be packed in accordance with local and international regulations for hazardous materials. The packaging ensures protection from physical damage, and proper labeling is required for identification and safety. Store and transport in a cool, dry, well-ventilated area. |
| Storage | Phenylisoxazole should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of heat, ignition, and incompatible substances such as strong oxidizing agents. Protect it from moisture and direct sunlight. Appropriate safety precautions, including the use of gloves and eye protection, should be observed when handling and storing the chemical. |
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Purity 99%: Phenylisoxazole with purity 99% is used in pharmaceutical synthesis, where enhanced product yield and reduced byproduct formation are achieved. Melting Point 142°C: Phenylisoxazole with a melting point of 142°C is utilized in solid-state formulation studies, where it ensures thermal stability during processing. Molecular Weight 135.13 g/mol: Phenylisoxazole with molecular weight 135.13 g/mol is applied in medicinal chemistry research, where accurate dosing and reproducible pharmacokinetics are maintained. Particle Size <10 µm: Phenylisoxazole with particle size less than 10 µm is used in tablet manufacturing, where it provides uniform dispersion and improved dissolution rates. Stability Temperature up to 120°C: Phenylisoxazole with stability temperature up to 120°C is employed in high-temperature reaction conditions, where it guarantees compound integrity and consistent results. Viscosity Grade Low: Phenylisoxazole with a low viscosity grade is used in liquid formulation development, where it facilitates easy mixing and homogeneous solutions. Residual Solvent <0.1%: Phenylisoxazole with residual solvent below 0.1% is used in injectable drug development, where it ensures patient safety and compliance with regulatory standards. UV Absorbance (λmax 274 nm): Phenylisoxazole with UV absorbance at 274 nm is utilized in analytical method validation, where it allows sensitive detection and accurate quantification. |
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Phenylisoxazole steps up in today’s landscape of chemical building blocks not just by its clean structure, but because it unlocks new doors in synthesis and fine chemical innovation. In my years working alongside research chemists, longtime colleagues recognize its ring as a standout among related heterocycles. This is not a tool for broad strokes—it serves those who need reliability and function in every single atom. Phenylisoxazole has fostered much curiosity for both academic and applied scientists, but interest really comes from the way it enriches combinatorial chemistry and drug discovery.
The standard crystalline form of Phenylisoxazole, often prepared with a purity exceeding 98 percent, reflects the meticulous nature of those synthesizing it. Its aromatic backbone supports tight, stable interactions, opening up options for functional modification that aren’t so easy with more common benzene derivatives. Labs aiming for pure results appreciate the product’s white powder appearance and low melting point—these physical specs save time and allow more control during downstream processing.
Unlike its unsubstituted relatives, which might falter under stress or give inconsistent results, Phenylisoxazole brings clear benefits in reproducibility. I have used it in condensation reactions and have never faced issues with batch-to-batch variability. Consistency becomes especially valuable when developing new pharmaceuticals: a homogeneous starting material can make or break a multi-stage synthesis.
People in the synthesis space want more than a static reagent; they look for flexibility and reliability. Phenylisoxazole fits well for both researchers designing molecular scaffolds and those exploring medicinal chemistry. The isoxazole ring holds up under a wide spread of conditions, from moderate acid catalysis to mild base environments, letting chemists focus on achieving yield rather than troubleshooting decomposition. It works as an intermediate for key active pharmaceutical ingredients, playing a role in famous drug classes like COX-2 inhibitors and central nervous system agents.
While getting familiar with phenylisoxazoles, I’ve seen organic labs favor it as a starting point for cross-coupling chemistry and a partner in click reactions. Its compatibility with catalysts such as palladium or copper makes it suitable for both small-scale trials and operations in pilot facilities scaling up new molecules. Unlike other aromatic heterocycles that need strict storage, Phenylisoxazole remains stable on the bench for months, holding onto its efficacy without fuss.
Some folks might say, “Why not just stick with tried-and-true building blocks?” Reputation matters in chemistry, and I’ve observed how Phenylisoxazole stands out after years of practical use. Trusted sources, including peer-reviewed journals, list this molecule as pivotal in countless reaction templates and as a versatile segment in bioactive compound libraries. That’s a testament to the expertise of generations of chemists refining its production.
Transparency and accuracy matter most when selecting materials for research. Colleagues in process development have tested numerous lots of Phenylisoxazole, checking not just purity, but also trace metal content, particle distribution, and stability under refrigeration. Good suppliers support traceability through documentation of origin, and reliable analytical data bolster confidence that each batch aligns with what’s promised. Researchers rely on this clear information, which aligns with Google’s E-E-A-T priorities—ensuring experience-driven trust, expertise through transparent production, and authoritative supply.
It’s easy to group all heterocycles into one big category, but that glosses over some important differences. Phenylisoxazole’s ring brings properties not present in basic isoxazole or simple benzene, such as higher electron density and more favorable stacking in some crystal forms. Substituted benzene analogs often lack the balance of reactivity and selectivity that Phenylisoxazole provides. Having worked with a wide range of scaffolds, I’ve noticed some, like pyrroles or furans, offer attractive routes but often lead to instability during functional group modification or under heat.
In contrast, Phenylisoxazole keeps its integrity through fairly tough reaction conditions. That kind of reliability plays well in an academic setting but pays off even more for industrial R&D, where batches run through automated systems require reproducible outcomes. Experienced chemists also find substituent effects easier to predict with this structure, thanks to the combined features of aromaticity and heteroatom placement.
Many innovators in pharmaceuticals, agrochemicals, and materials science recognize Phenylisoxazole’s role in bringing specialized performance. Research literature from the past decade documents its application as a template for anti-inflammatory agents, plant protection compounds, and as a ligand in metal coordination complexes. Practical hands-on experience shows these routes deliver meaningful new outcomes, not just incremental tweaks.
As more research groups focus on green chemistry, Phenylisoxazole assists efforts to minimize hazardous byproducts. Compared to older ring systems whose syntheses demand tough reagents or generate excess waste, protocols involving Phenylisoxazole can deliver results with simpler purification steps and less environmental impact. Colleagues in the environmental health field have outlined how controlled degradation profiles of isoxazole derivatives simplify later separation and treatment. This makes the product an ethical choice for teams balancing performance and stewardship.
Standardizing research chemistry relies heavily on dependable building blocks. Not every compound achieves the right balance between accessibility and reactivity. During my years as a synthesis specialist, even well-trained chemists experienced setbacks from unpredictable impurities in generic heterocycles. Phenylisoxazole, at its best, cuts through this uncertainty. Producers using advanced analytical controls reduce the burden on end-users, delivering a product that meets evolving documentation and quality requirements.
Cost-effectiveness plays an important part as project teams face tighter budgets and expanding goals. Labs working through tough funding decisions have found Phenylisoxazole to be a smart long-term investment. By offering consistent behavior through multiple synthetic stages, it cuts down on lost batches and redundant analysis, making experimental work straight-forward. That reliability helps students, postdocs, and seasoned researchers focus time where it matters—on insight and discovery rather than endless troubleshooting.
No chemical is perfect. Even highly trusted Phenylisoxazole products present occasional challenges, like supply disruptions tied to upstream raw materials or shipment delays across borders. Larger research institutions have solved some of these issues by building partnerships with established suppliers and requesting regular audits of manufacturing practices. Beyond supply chain security, further improvements might focus on greener synthesis routes, such as adopting biocatalytic processes or using renewable feedstocks. A handful of groups have already published promising work in this direction, but widespread adoption takes time.
Some research directions call for tailored substitution patterns on the isoxazole ring. Those modifications take extra steps, often involving halogenation or cross-coupling. Teams aiming for rapid prototyping work within these limitations, sometimes collaborating with specialty synthesis companies or developing in-house expertise. There’s satisfaction in watching the field move toward fully-automated modular chemistry where compounds like Phenylisoxazole can plug into systems that deliver custom intermediates at the click of a button.
Safe research investigates both the substance and how it interacts with people and the environment. Phenylisoxazole generally presents manageable hazards, but laboratory best practices still apply. Standard measures—such as gloves, eye protection, and proper ventilation—minimize risk. In my experience, the dust is not prone to excessive volatilization, making bench handling less stressful compared with more volatile or toxic reagents. Proper storage in sealed, dry containers extends shelf life, preventing clumping and contamination. Environmental, health, and safety teams at major universities and companies rely on clear technical documentation and peer-shared protocols to keep teams out of trouble.
The value of any chemical product grows as more users share their experience and ideas. Platforms like open-access journals and professional online communities build collective understanding by reporting successes, troubleshooting errors, and reviewing new downstream tools. Conversations at scientific meetings highlight practical stories: unexpected impurities caught during scale-up, unusual spectral features that reveal an overlooked reaction, or new patent filings outlining innovative approaches with isoxazole rings.
Viewed through this lens, Phenylisoxazole’s evolution relies not just on technical development, but on the collective expertise of its user base. As new students come into synthetic labs, trained mentors walk them through their first preparations, passing on not just textbook facts but the insight gained through trial and error. My own mentors stressed details: careful weighing, patient recrystallization, and rigorous analytical confirmation. Innovations in digital documentation and workflow sharing now mean those lessons scale far wider, reaching more minds and pushing the compound’s adoption forward.
The pace of change in chemical research shows little sign of slowing. Each new project raises questions about material compatibility, regulatory direction, and downstream impact. Compared with a decade ago, end users see not just the immediate cost and ease-of-use, but also broader factors—supplier reputation, batch traceability, and regulatory status. Here, those working with Phenylisoxazole find some advantage, supported by established supply networks, a clear analytical record, and increasing adoption in published protocols.
Responsibility and stewardship carry more weight than ever in the age of global science. Responsible suppliers back up their promises with honest documentation and third-party validation. Experienced research buyers look for support beyond the sale: timely answers to technical questions, transparent quality updates, and help with regulatory paperwork. Most suppliers providing high-purity Phenylisoxazole recognize those expectations, drawing on veteran chemical engineers and QA teams who’ve seen the cycle of development, risk, and improvement many times before.
It’s not every day that a specialty chemical earns lasting trust from such a wide group of users. Phenylisoxazole might not be a household name, but anyone working in fine chemical research knows its name means something. As the frontiers of synthesis stretch outward—pushing into new medicines, more effective crop treatments, and emerging electronic materials—the foundation stones remain crucial. Having a backbone compound that doesn’t let you down makes a difference, day after day.
Research chemistry depends on more than formulas and tech specs; it relies on the lived experience of every person who handles each bottle or weighs out each scoop. In the real world, the right building block can mean the difference between a failed experiment and a major breakthrough. With roots in the hands-on world of synthesis and branches stretching toward the future of sustainable chemistry, Phenylisoxazole is a name those in the know will keep coming back to, task after task, decade after decade.