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4-Bromo-6-Trifluoromethyl-Indazole

    • Product Name 4-Bromo-6-Trifluoromethyl-Indazole
    • Alias 4-Bromo-6-(trifluoromethyl)-1H-indazole
    • Einecs 821-525-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
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    • Manufacturer Sinochem Nanjing Corporation
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    Specifications

    HS Code

    225601

    Chemical Name 4-Bromo-6-Trifluoromethyl-Indazole
    Molecular Formula C8H4BrF3N2
    Molecular Weight 265.03 g/mol
    Cas Number 1053654-43-3
    Appearance Off-white to pale yellow solid
    Melting Point 102-106°C
    Purity ≥98%
    Synonyms 4-Bromo-6-(trifluoromethyl)-1H-indazole
    Solubility Soluble in DMSO, DMF; limited in water
    Storage Conditions Store at 2-8°C, away from light and moisture
    Smiles FC(F)(F)c1ccc2n[nH]cc2c1Br

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    More Introduction

    Introducing 4-Bromo-6-Trifluoromethyl-Indazole: A Closer Look

    A Fresh Perspective on Indazole Derivatives

    Over the past decade, advances in drug discovery and materials science have opened new chapters for heterocyclic compounds. Among them, 4-Bromo-6-Trifluoromethyl-Indazole stands out, not just for its unique structure, but also for the versatility it brings to research and industry. In my own experience working in a multidisciplinary lab, the search for reliable building blocks often leads researchers through a maze of options. Only a handful of these actually deliver the performance and precision needed for challenging synthetic targets. This compound has made its mark among teams aiming to push the boundaries of medicinal chemistry.

    Understanding the Heart of the Molecule

    With a bromine atom at the fourth position and a trifluoromethyl group at the sixth, 4-Bromo-6-Trifluoromethyl-Indazole offers a distinct chemical fingerprint. On paper, the molecular formula means little to most people. In practical terms, those substituents add more than just bulk to the indazole ring—each group shapes electronic properties and reactivity. Bromine brings weight and reactivity, making it ready for advanced coupling reactions. That is a trait most synthetic chemists crave, particularly in the early stages of drug design. The trifluoromethyl group locks in stability and modulates lipophilicity, both crucial for preparing molecules meant to slip through biological membranes.

    How Labs Put It to Work

    Day to day, researchers use 4-Bromo-6-Trifluoromethyl-Indazole as a starting material for complex molecules. Its readiness for Suzuki and Buchwald-Hartwig couplings makes it a favorite among both academics and industry scientists. In my own time synthesizing heterocycles, I’ve seen project leads reach for this indazole again and again—not because it’s a household name, but because it offers consistent results. The bromine replaces easily in carefully chosen cross-coupling reactions. At the same time, the trifluoromethyl group holds its ground through tough conditions, offering a shortcut past tedious protection and deprotection steps.

    Real Challenges, Real Progress

    One core problem in modern drug discovery lies in tuning the balance between molecule stability and activity. Introducing electron-withdrawing or -donating groups at just the right place in a ring system isn’t a matter of trial and error—the process demands parts that both work and last. 4-Bromo-6-Trifluoromethyl-Indazole fits this niche well. By holding onto key physical characteristics, it maintains stability for storage, transport, and further reactions. Few comparable indazole derivatives offer the same package of reactivity and robust shelf life, limiting how far a project team can push a new synthetic route before heading back to the drawing board.

    Comparing Alternatives: What Actually Makes the Difference

    Plenty of building blocks compete for shelf space in synthetic labs. For example, regular 6-substituted indazoles without the bromine typically fall short during late-stage diversification. The same goes for simple brominated indazoles that lack additional electronic tuning. Where 4-Bromo-6-Trifluoromethyl-Indazole pulls ahead is in its combination of selectivity and stability. The molecule doesn’t fall apart when the heat is on—literally or figuratively. For teams working on high-throughput screening or optimization, those small details turn into big advantages, saving weeks that would otherwise go to troubleshooting or repeat purifications.

    The Role in Medicinal Chemistry

    Recent work in medicinal chemistry leans heavily on the modular design of new chemical entities. With more elaborate targets emerging every year, chemists need reliable reagents that speed up SAR (structure-activity relationship) studies. When using this indazole derivative, modifications at the fourth and sixth positions open doors for attaching a wide range of substituents. That flexibility supports rapid testing and adaptation without the bottleneck of unwanted side reactions. Teams investigating kinase inhibitors, serotonin antagonists, or other small-molecule therapeutics turn to this compound for its track record in yielding well-defined products with high purity. Its reputation in the literature, especially in peer-reviewed case studies, reinforces the sense that this is more than an off-the-shelf intermediate.

    Specification That Matters in Practice

    Anyone who’s stood over a balance in a chemistry lab and weighed out a new batch knows the value of material purity. Nobody wants to troubleshoot a reaction and discover traces of starting material or lingering byproducts. In real-world sourcing, product batches of 4-Bromo-6-Trifluoromethyl-Indazole show high purity by HPLC analysis. Typical lots arrive as fine off-white powders that dissolve predictably in most polar organic solvents. That saves both time and solvents, something I care about both for financial and environmental reasons. Researchers see more consistent reaction outcomes when using material sourced from reputable suppliers. That’s not just a footnote—it’s critical to ensuring reproducibility and reliable yields.

    What Sets the Compound Apart in Synthesis

    Classical indazole derivatives have served medicinal chemists for decades. The new generation, including 4-Bromo-6-Trifluoromethyl-Indazole, reflects advances in understanding both reaction mechanisms and application-driven synthetic design. One advantage here comes from the interplay between bromine and the trifluoromethyl group. While bromine is a familiar tag for cross-coupling, the electron-withdrawing character of the trifluoromethyl group stabilizes certain intermediates and intermediates, creating more favorable conditions for selective reactions. That leads to improved yields without the need for exotic conditions or added catalysts. From my time collaborating with synthesis teams, I’ve seen this translate into shorter timelines and higher reaction success rates—giving busy project managers one less thing to worry about.

    Impact on Lab Workflow

    Replacing less robust indazoles with this particular derivative can streamline the daily grind in chemistry labs. Stable precursors mean fewer failed attempts and less time troubleshooting. Managing stocks becomes simpler because the compound doesn’t require special storage beyond standard precautions for chemicals of its class. Since many projects juggle dozens of intermediates, anything that reduces the chance for inventory headaches brings a real improvement.

    Broader Reach: Beyond Pharmaceuticals

    Although most of the excitement comes from drug discovery, other industries have started tapping into the potential of indazole derivatives. Agrochemical developers and advanced materials researchers use compounds like 4-Bromo-6-Trifluoromethyl-Indazole for functionalizing catalysts, surfactants, and polymers. These applications call for molecules that can survive demanding synthetic processes without losing integrity or performance. Reflecting on conversations with colleagues in material science, the ability to introduce highly controlled modifications often spells the difference between a novel additive that actually performs and one that remains just a promising structure on paper.

    Environmental and Safety Considerations

    Looking at the realities of laboratory life, handling safety and minimizing environmental impact aren’t just buzzwords. No compound deserves a spot in routine research unless it behaves predictably. 4-Bromo-6-Trifluoromethyl-Indazole performs predictably under standard protocols for organic solids. Proper lab safety measures—gloves, goggles, fume hoods—cover the bases here. Disposal follows the established routes for indazole-based compounds, which helps ensure compliance with environmental standards. Reliable data from both suppliers and independent safety evaluations keeps researchers informed about best practices and potential risks.

    Supply Chain Reliability

    Thinking back to the rocky months during supply chain disruptions, nothing creates headaches for R&D like waiting for a critical reagent. What makes a real difference with this compound is its track record for availability from multiple synthesis routes. Multiple manufacturers have scaled up processes using modern batch and flow techniques, so delays are less likely to derail a long-term project. Open communication between suppliers and research teams keeps expectations realistic and project timelines on track. Reliable delivery eliminates the hand-wringing and lets teams focus on the science.

    Spotlight on Research Reproducibility

    Reproducibility in synthetic chemistry sits at the center of scientific progress. Repeating results in different labs doesn’t just confirm findings; it propels careers and discoveries. When using 4-Bromo-6-Trifluoromethyl-Indazole, researchers see high reproducibility across different batches and reaction scales. This dependability stands in contrast to some specialty derivatives that vary from vendor to vendor or from one batch to another. Establishing confidence in results secures grants, supports publication, and encourages bolder exploration of new molecular designs.

    Cost Vs. Value in Research Budgets

    Balancing budgets while pushing forward scientific discovery remains a constant concern in research. Teams face choices—spend more now to avoid greater costs or accept cheaper options and risk wasted time. My own experience has shown that compounds like 4-Bromo-6-Trifluoromethyl-Indazole, offering both versatility and stability, pay for themselves through fewer failed runs and more definitive outcomes. Labs achieve better value by reducing both hands-on time and the number of repeated syntheses. Despite slightly higher initial pricing than generic indazole types, long-term efficiency often offsets the cost.

    New Synthetic Possibilities

    Emerging synthetic techniques, such as photoredox or transition metal-catalyzed direct arylation, raise the bar for intermediate performance. 4-Bromo-6-Trifluoromethyl-Indazole answers this call by serving as a robust participant in these strategies. Researchers report that the combination of bromine and trifluoromethyl extends reaction options compared to single-substituent molecules. The control and selectivity possible with this compound can mean the difference between a high-profile publication and a dead-end result. From collaboration with academic innovators, I’ve seen research groups leverage this adaptability to open new lines of inquiry and develop novel lead compounds.

    Streamlining Scale-Up

    What works in a 10 mL flask often stumbles at the next scale. Labs aiming to step their projects from milligram to gram quantities need intermediates that don’t create new problems with increased volume. 4-Bromo-6-Trifluoromethyl-Indazole handles this jump well, a fact that teams engaged in process optimization appreciate. Scalability brings knock-on benefits for startups and pharmaceutical companies planning longer-term pipeline development. The practical feedback loop between bench synthesis and pilot production becomes smoother, reducing uncertainties about regulatory submission quality or downstream manufacturing consistency.

    Toward Greener and Safer Synthesis

    Greener chemistry isn’t just about using less hazardous materials; it’s about finding reliable routes that cut waste and minimize unnecessary steps. Using intermediates with robust stability usually means fewer purification rounds and tighter reaction controls. 4-Bromo-6-Trifluoromethyl-Indazole enables researchers to cut down on hazardous reagents, since its selective properties allow for more tailored conditions and less byproduct formation. Environmental stewardship in chemical research depends on choices made at every stage, from reagent selection to waste handling. With compounds that extend the life of catalysts and stand up under gentle conditions, everyone benefits—from budget managers to lab safety officers.

    Supporting Early-Career Researchers

    Reflection on my years as a graduate student reminds me how much newcomer success depends on clear, dependable reagents. Indazoles like this remove one source of uncertainty for those learning the art and science of synthesis. Students and early-career researchers can focus on the bigger questions of reaction design, not rescue missions for faulty intermediates. Better reagents support steeper learning curves, more confident troubleshooting, and greater enthusiasm for the craft of chemistry. The ripple effect extends across departments as higher quality data makes its way into discussions, presentations, and publications.

    Industry Trends and the Path Forward

    Markets for specialty ingredients and advanced intermediates have evolved rapidly over recent years. Pharmaceutical, agrochemical, and materials science companies all seek out robust, well-characterized building blocks to speed up research and innovation. 4-Bromo-6-Trifluoromethyl-Indazole keeps up with these industry needs by supporting both small-scale innovation and large-scale production. Looking ahead, tighter regulatory frameworks and increased demand for sustainable, traceable chemicals will test all intermediates. Only those with proven profiles in stability, adaptability, and safety will remain in widespread use. This indazole’s growing presence in chemical catalogs and cited studies suggests it is here to stay.

    Potential Improvements and Solutions to Current Issues

    While the current state of availability and utility for 4-Bromo-6-Trifluoromethyl-Indazole addresses many lab demands, room for improvement always exists. Continuous dialogue between researchers and suppliers drives refinements in packaging, batch documentation, and impurity profiling. Electronic lab notebooks and digital traceability can bolster confidence in results shared across teams and institutions. Broader supplier certification and transparent quality control would close the gaps for labs operating under exacting GLP or GMP standards. Collaboration on recycling or alternative production methods could further enhance sustainability, moving the industry closer to a true circular economy model for specialty chemicals.

    Why the Details Matter

    Precision in research comes down to the small things: choosing parts that don’t just work, but work well and reliably. 4-Bromo-6-Trifluoromethyl-Indazole exemplifies how much can be gained from investing in intermediates that raise the level of what’s possible in synthesis. Its role in streamlining workflow, improving safety, and opening new research possibilities demonstrates the true value of specialized building blocks, even if they may seem, at first glance, like just another chemical on the shelf. For researchers, educators, and innovators looking to get the most out of their resources, this compound shows how thoughtful selection pays off, run after run, project after project.