|
HS Code |
765169 |
| Chemicalname | 5-Bromo-1,2-Benzisoxazole |
| Casnumber | 5118-13-8 |
| Molecularformula | C7H4BrNO |
| Molecularweight | 198.02 |
| Appearance | Off-white to light beige powder |
| Meltingpoint | 99-103°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically ≥98% |
| Synonyms | 5-Bromo-benzisoxazole |
| Smiles | Brc1ccc2onc2c1 |
| Inchi | InChI=1S/C7H4BrNO/c8-5-1-2-6-7(3-5)9-4-10-6/h1-4H |
As an accredited 5-Bromo-1,2-Benzisoxazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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Anyone who has spent hours bent over a lab bench knows that progress in chemical synthesis comes down to picking the right starting materials. Some compounds only do a single job, but others open up far more possibilities. 5-Bromo-1,2-Benzisoxazole fits that rare second group. This product has steadily gained recognition among researchers, process engineers, and industrial chemists alike, as a hard-working ingredient that brings a lot to the table without demanding extra steps in the workflow.
What stands out about 5-Bromo-1,2-Benzisoxazole is what it allows in the laboratory. The bromo-substituent at the 5-position turns this molecule into a reliable handle for modern cross-coupling chemistry. In rooms filled with glassware, steam, and the low buzz of planning, organic chemists recognize this structure as more than a name—it's a ticket to constructing larger, more complex molecules. Countless synthesis projects, ranging from bench-scale to full industrial production, rely on it as a trusted intermediate, especially where fine details of molecular architecture make all the difference.
5-Bromo-1,2-Benzisoxazole looks almost modest in structure. It places a single bromine atom on the benzisoxazole ring, right at the five position. This choice isn't just about aesthetics. For people in synthetic chemistry, the physical placement of that bromo group gives the molecule its punch. It acts as the go-to leaving group for Suzuki, Stille, or Heck reactions. No one in a lab shuffles through order forms hunting for mysterious new intermediates each time a new project crops up. Chemists value materials that behave predictably and adapt to a wide range of transformations. By placing that bromine in just the right spot, 5-Bromo-1,2-Benzisoxazole makes cross-coupling reactions faster and cleaner. It sidesteps a lot of the wasted effort that comes from byproduct formation or unwanted side reactions.
The actual appearance is a pale solid, easy enough to handle or to weigh out in a dimly lit corner of a research lab. Most people who handle it can tell a material is well-prepared simply by looking for a pale consistency and the absence of visible impurities. With a molecular formula of C7H4BrNO, it balances the stability needed for shipping and storage with the reactivity needed for downstream transformations. Even after years working across different industries, that particular blend stands out as rare. You do not want to fight with unstable or overly hazardous intermediates during scale-up, just to shave a few steps from a process.
Many in the field of chemical synthesis can recall the emergence of benzisoxazoles as cornerstones for medicinal chemistry and agrochemical programs. Many blockbuster drugs and key crop protectants stem from inventive use of these heterocyclic motifs. Adding a bromo to the five position creates new reactive possibilities. You can switch out that group with boronic acids, stannanes, or amines, moving towards products that matter—pharmaceutical leads, custom materials, or biological probes. In my own work helping scale up small batch syntheses for local start-ups, I saw how the reliability of this intermediate ended up saving weeks of trouble. The same batch could move from small flask to pilot plant without revisiting core reaction conditions. That continuity removes stress from chemical manufacturing.
For students learning the processes behind drug discovery, seeing a product like 5-Bromo-1,2-Benzisoxazole reveals how decisions at the molecular level influence everything downstream. Selectivity, reproducibility, and clean functional group installation define successful routes for advanced therapeutics or specialty chemicals. Publications in organic process journals routinely highlight similar halogenated heterocycles as backbone intermediates in syntheses targeting everything from psychiatric medications to complex ligands for catalysis.
Some compounds look good on paper, but falter in the real world: tough to purify, sensitive to air or moisture, or just dogged by low yields and byproducts. 5-Bromo-1,2-Benzisoxazole stands apart by handling all that pragmatic chemistry—easy to store, tolerant of a range of storage conditions, and still just as reactive when needed. Having worked with more sensitive compounds in the past, I appreciate just how few headaches these stable intermediates save both in academic and industrial labs.
The landscape is crowded with different benzisoxazole derivatives. Each position on the ring offers a chemist a new avenue for reactivity. Chlorinated or fluorinated analogs pop up from time to time, but they do not always deliver the same balance. Bromine sits in a Goldilocks position: reactive enough for functionalization, yet not as harsh or unpredictable as iodine. Tutorials and review articles in leading chemistry journals echo these points, noting how bromo compounds generally form the 'sweet spot' for many C-C or C-N bond formations.
Chlorinated analogs sometimes wind up requiring harsher conditions, risking degradation of sensitive parts of the molecule. On the other hand, iodinated versions can be more expensive and challenging to source in bulk. Both options often bring added toxicity or regulatory scrutiny. By comparison, brominated versions like 5-Bromo-1,2-Benzisoxazole have a track record for easy adaptation and scale-up—a significant edge in pharmaceutical and specialty materials work.
In my own research and collaborations with industrial partners, the question often arises: what about direct nitration, or amination, instead of using the bromo derivative? In practice, direct functionalization is less predictable, yielding variable results batch to batch and introducing more workup and optimization headaches. The 5-bromo building block offers a consistent, stepwise entrance to a series of targeted modifications, whether you aim for direct arylation, installation of electron-donating groups, or selective reduction. That predictability shows up in fewer failed syntheses, higher yields, and in my own experience, happier chemists.
Most research papers or conference posters describing new drug candidates, innovative ligands, or photoactive materials draw on building blocks like 5-Bromo-1,2-Benzisoxazole. In the pharmaceutical industry, a single intermediate that supports dozens of downstream modifications helps shave months off the discovery process. Chemists can probe structure-activity relationships, pushing and pulling substituents to find the optimal pharmacological profile, all made easier by the modular strategies enabled by this building block.
Sitting at the junction of reproducibility and flexibility, 5-Bromo-1,2-Benzisoxazole opens doors for custom syntheses. Medicinal chemists frequently use it in the search for new neurological and antimicrobial agents. The presence of the benzisoxazole core in several clinically-relevant drugs underpins demand. Custom molecule projects for diagnostics or specialty polymers also value this compound—a recurring theme in technical meetings and patent literature.
Scaling up from lab gram quantities to multi-kilogram industrial batches calls for intermediates that can take the heat. During the transition from early discovery to full plant production, this product has never failed the consistency test. Most colleagues working in process development prefer to keep known, dependable compounds in the toolkit. I recall an extensive optimization project where every trial run with this bromo intermediate gave clean chromatograms and scalable reaction profiles, while a similar batch using a 5-chloro analog never quite hit the same marks.
Every chemical presents choices—and each comes with its own environmental and safety factors. The bromine atom on this molecule brings a balance between reactivity and practical handling. As regulations evolve, the industry keeps an eye on greener ways of introducing bromo groups, as well as more sustainable manufacturing processes. Adapting to advances in purification, solvent recovery, and minimized waste always sits at the top of expert discussions. Many forward-thinking suppliers now invest in production methods that cut down on hazardous waste, optimize energy use, and deliver product matched to high-purity benchmarks, an issue that matters deeply for downstream applications in drugs and advanced materials.
Safety data—as in all halogenated aryl intermediates—means appropriate gloves, goggles, and ventilation. After years of bench work, I have found that a solid, stable compound like 5-Bromo-1,2-Benzisoxazole helps reduce risk when compared to more volatile or unstable alternatives. Fewer toxic byproducts or waste streams result during use, and the molecule rarely brings surprises in standard lab handling.
Regulatory frameworks around the globe continue evolving, particularly for intermediates with medicinal or agricultural relevance. Years in the field have taught me not to underestimate the value in working with a product whose compliance record can stand up to the scrutiny of regulatory agencies in Europe, North America, and Asia. As more innovations in drug design, diagnostics, or crop protection emerge, the backbone supplied by this brominated benzisoxazole holds steady.
For those concerned with waste, greener cross-coupling reactions (for example, using water-soluble bases, non-toxic ligands, or lower temperature conditions) pair reliably with this intermediate. That versatility allows chemists—be they students or veterans—to experiment and refine their processes while keeping environmental impact in mind. Reducing reliance on hazardous solvents, employing single-pot processes, and recycling starting materials have all appeared in both trade magazines and peer-reviewed papers as growing practices, supported by intermediates just like this.
In chemical manufacturing and research, small problems magnify during each stage of the process. An unstable or unpredictable intermediate means delays, increased costs, or even regulatory noncompliance. Using a well-understood product such as 5-Bromo-1,2-Benzisoxazole cuts those risks. Large contract research organizations and smaller startups alike report consistent outcomes, shorter time-to-market, and less troubleshooting when projects begin from this foundation.
Some would say a commodity intermediate does not need scrutiny or careful choice. In my own experience, it's that exact assumption that can unravel a promising new drug project or specialty application. Having worked through late-night troubleshooting in manufacturing suites and research labs alike, I know the peace of mind that comes from a product with a strong performance record. Long supply chains and tighter budgets only highlight these advantages.
From a practical standpoint, minimizing costs around purification and analysis always matters. Using 5-Bromo-1,2-Benzisoxazole as a precursor streamlines both analytical checks and process control. Analysts find fewer trace impurities and consistent melting points. In pharmaceutical applications, even small deviations in impurity profiles trigger red flags with regulatory agencies. Drawing from past projects, I can confidently say that this intermediate reduces the likelihood of those costly surprises.
New trends in chemical R&D focus on expanding cross-coupling technology, sustainable synthesis, and integration with automation. Modern robotic synthesis lines increasingly rely on tried-and-true intermediates. For high-throughput screening and automated reactions, product consistency is not a luxury, it is a requirement.
As the world moves toward greener chemistry, more professionals look for ways to introduce complexity into molecules with fewer resource and energy demands. 5-Bromo-1,2-Benzisoxazole plays into several of these goals. It sits at the center of new ligand development, helps construct chiral building blocks, and remains a staple in the electronic materials sector. Process development teams cite its compatibility with emerging green solvents and alternative energy sources, such as microwave or flow reactors, further reducing operational footprints.
Younger chemists eager to craft the next generation of biologically active molecules benefit from direct access to reliable intermediates. Training programs now emphasize green metrics, cost controls, and safety, all areas where 5-Bromo-1,2-Benzisoxazole stands out. Its known safety profile, broad adoption across fields, and adaptability to new synthetic platforms highlight why it stays in demand, even as novel approaches emerge.
Supply reliability also weighs heavily, especially as global disruptions have forced manufacturers to rethink sourcing. Products like this, with established global supply lines and decades-long literature precedent, become key anchors for long-term R&D planning. Colleagues working in procurement and supply assurance regularly point out the less tangible, but crucial, value in maintaining robust inventories of foundational intermediates.
It takes years of running reactions, troubleshooting unexpected problems, and navigating the rigorous demands of quality control to understand the difference a dependable intermediate brings. The significance of 5-Bromo-1,2-Benzisoxazole in today's chemical landscape comes not from its novelty, but from a long list of projects—from failed screens salvaged in the late hours to successful launches of new products—that relied on its utility.
Professional organizations, such as chemical societies and regulatory advisory panels, often cite compounds like this for their foundational role. They help standardize best practices, anchor curricula for new generations of synthetic chemists, and form the basis of many peer-reviewed studies. This shared track record allows researchers to look not just at their immediate goals, but to build on the shoulders of well-understood chemistry.
In my experience, the trust built around a consistent product spills over to every step in discovery, scale-up, and commercialization. The legacy and adaptability of 5-Bromo-1,2-Benzisoxazole mean that both established professionals and newcomers can focus more on creative problem-solving and less on guesswork about batch variability or unexpected reactivity.
For new startups seeking fast tracks to proof of concept, or academic teams attempting total synthesis of novel compounds, the foundation remains the same: a manageable, reliable, and well-documented intermediate. As the number of synthetic routes and potential end-uses keeps growing, professionals continue to rely on core building blocks to avoid costly and time-consuming detours.
The future likely brings even greater integration between data-driven process monitoring and legacy intermediates like 5-Bromo-1,2-Benzisoxazole. Combining the power of predictive analytics—now a growing trend in both GMP and high-throughput labs—with products backed by decades of performance data can only accelerate safe, efficient innovation. More tight-knit feedback loops between supplier and researcher, focusing on batch-to-batch quality assurance and transparent documentation, should continue to deliver value.
Not every compound earns its place as a mainstay in chemical synthesis. Careers get built, processes refined, and breakthroughs achieved with the help of certain structures that never attract the spotlight but save hours, money, and risk. 5-Bromo-1,2-Benzisoxazole stands firmly in that group. Its continued role in the progress of new materials, medicines, and industrial solutions reflects more than just reactivity; it reflects the judgment of thousands of professionals who make things happen every day.