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HS Code |
656579 |
| Product Name | 3-Bromo-7-Fluoro-1H-Indazole |
| Cas Number | 1246121-45-6 |
| Molecular Formula | C7H4BrFN2 |
| Molecular Weight | 215.03 |
| Appearance | Off-white to light brown solid |
| Purity | Typically ≥97% |
| Smiles | c1cc2c(c(c1F)Br)nn(C2) |
| Inchikey | CAZGQBCPRTEAAM-UHFFFAOYSA-N |
| Synonyms | 1H-Indazole, 3-bromo-7-fluoro- |
| Solubility | Soluble in organic solvents |
| Storage Temperature | 2-8°C |
| Mdl Number | MFCD13188025 |
As an accredited 3-Bromo-7-Fluoro-1H-Indazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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| Shipping | |
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Every new compound unlocks fresh opportunities in scientific research. 3-Bromo-7-Fluoro-1H-Indazole offers something unique. Chemists, material scientists, and pharmaceutical developers have turned to indazole derivatives for decades, searching for that extra avenue of selectivity, potency, or novelty within their projects. My own first encounter with indazoles came during a medicinal chemistry project, and it was clear, even then, that these compounds held remarkable structural promise.
3-Bromo-7-Fluoro-1H-Indazole stands out with clear molecular design—precisely planned halogenation where both bromine and fluorine serve distinct purposes. The indazole core, a familiar scaffold, serves as a launching pad for further modifications. In this structure, the bromine atom is positioned on the third carbon while fluorine anchors at the seventh. What does this accomplish? A pattern that influences electronic distribution across the molecule. This adjustment paves the way for more predictable reactions, making the compound an attractive intermediate for the synthesis of novel analogs.
Those who measure out reagents by the milligram will appreciate a dry, crystalline substance that can be weighed accurately and resists clumping, thanks to the stable nature of both the indazole ring and halogen substitutions. Purity isn’t a vague promise with this compound—producers offer analytical data like NMR and HPLC, which gives researchers confidence that each batch meets the standards demanded in advanced laboratories.
Some molecules come with a reputation for unpredictability. Indazoles, by nature, often introduce stability alongside functional versatility. Adding both bromine and fluorine to the indazole skeleton doesn’t just offer another indazole to the mix—this arrangement advances possibilities for late-stage derivatization and selective coupling reactions. In the pharmaceutical sphere, medicinal chemists target these halogenated spots using palladium catalysis and other coupling strategies, knowing that both the bromine and fluorine substitutions bring a certain reactivity profile.
In my former role at a university drug discovery center, candidates like 3-Bromo-7-Fluoro-1H-Indazole gave our teams confidence that small modifications would remain localized—few unwanted surprises in reactivity, which means fewer wasted resources. The confidence to plan synthetic routes, track progress via recognizable shifts in NMR, and build on a reliable skeleton saves both time and cost.
Chemical research rarely fits neat categories. 3-Bromo-7-Fluoro-1H-Indazole supplies building blocks for drug discovery, agrochemicals, materials science, and academic curiosity. In the lab, it often takes the role of a precursor—not just any precursor, but one which engineers can further elaborate into kinase inhibitors, CNS-targeted compounds, or imaging agents. The fluorine’s presence can tune lipophilicity or metabolic stability, key considerations for lead optimization in drug discovery.
Those developing new organic electronic materials, such as OLEDs, also find utility here. The substitution pattern provides predictable conjugation behavior. I’ve spoken with colleagues in the field who reach for fluorinated indazoles to tweak emission wavelengths or charge mobility. What’s consistent in these conversations: this compound’s balance between reactivity and persistence proves valuable during scale-up.
Educational settings also benefit. Synthetic labs that need to teach about halogen dance reactions, Suzuki or Buchwald-Hartwig cross-coupling, or advanced purification techniques find that 3-Bromo-7-Fluoro-1H-Indazole presents real-world relevance without excessive hazard. It’s a straightforward way to introduce fledgling chemists to concepts like regioselectivity and strategic scaffold modification.
Not every indazole compound is created equal. Many researchers once defaulted to simple indazole, only to hit dead ends when fine-tuning solubility or pursuing higher target selectivity. Here, the addition of a bromine at the three-position and a fluorine at the seven-position enables attachments at both opposite poles of the molecule after further transformation. Contrasts often come into play in drug design—fluorine can intercept metabolic oxidation, while bromine serves as a handle for cross-coupling chemistry.
I recall one instance where our team ran headlong into metabolic instability. Simple indazoles were chewed up by liver enzymes, compromising their effectiveness. Swapping to 3-Bromo-7-Fluoro-1H-Indazole altered the metabolic fate of our test molecules—suddenly, clearance slowed and activity profiles stabilized. Reports from the broader field mirror this experience: fluorinated and brominated aromatics often outlast their unsubstituted peers in biological systems, enduring longer in both in vivo and in vitro contexts.
Compare this compound with its monohalogenated counterparts. The dual substitution doesn’t just double the options, it recasts the chemical landscape. Both substitutions open up more choices during synthesis. For teams who’ve struggled to achieve selectivity or consistent reactivity with other analogs, the difference isn’t just theoretical—it’s evident once reactions run faster, yields improve, and purification gets easier.
When I handle reagents in the lab, there’s nothing quite as frustrating as inconsistent purity or variable melting points. Early on in my career, I learned the importance of reliable suppliers and standardized quality controls. 3-Bromo-7-Fluoro-1H-Indazole, manufactured under tight analytical oversight, addresses this head on.
Reputable suppliers don’t just promise high purity; they routinely furnish NMR spectra, melting point data, and chromatograms. In one study, a research group delivered three consecutive batches from different lots—each run gave parallel results. Chromatography signals lined up, and reaction yields matched the published methods. Such reproducibility means less troubleshooting, faster project timelines, and more reliable data when writing up results or planning patent applications.
Researchers share concerns about shelf life and storage. The molecule’s construction means it stands up to standard refrigeration, and short exposures to room temperature during weighing or transfer don’t lead to degradation or coloring. For labs without high-end environmental controls, this stability cuts stress and minimizes waste. I remember keeping other, less robust compounds locked away in the coldest parts of our fridge, worrying about every extra minute out of storage. With this molecule, those worries diminished.
Lab workers always think about safety. 3-Bromo-7-Fluoro-1H-Indazole’s hazard profile sits comfortably alongside standard aromatic and halogenated reagents. It lacks many of the severe hazards common to diazonium salts or some nitroaromatics—another point in its favor. Personal protective equipment and proper fume hood use suffice for risk mitigation.
Its relative lack of volatility means bench chemists won’t inhale vapors during handling. Spills can be swept up without panic, and disposal protocols follow familiar processes for halogenated organic materials. I’ve spoken with several lab managers who appreciate not having to draft extra emergency procedures just for this one bottle. This reliability may seem minor, but it’s the kind of thing that saves time and keeps morale high in busy research settings.
It’s common for budgets to strain under the cost of specialty chemicals, particularly when reordering becomes frequent due to loss or spoilage. The physical resilience of 3-Bromo-7-Fluoro-1H-Indazole—rarely impacted by mild humidity, light, or casual handling—lets labs maximize every gram purchased. Over time, this makes a tangible difference, letting academic groups, startups, and industry research teams stretch limited funds farther.
Each new molecule added to the researcher’s toolkit pushes science forward. 3-Bromo-7-Fluoro-1H-Indazole doesn’t just fill space on chemical shelves; it gives teams open doors to develop novel therapies, advanced agrochemicals, or next-generation electronic devices. Its clear structure and reliable physical characteristics light the way for innovation, not just incremental change.
As the world faces mounting challenges in health care, food security, and sustainable materials, researchers must work with ingredients whose track records support ambitious projects. Basic research molecules like this one play unsung roles—enabling reference experiments, offering functionalized starting points, and holding up under repeated experimental cycles. In practice, these traits reduce learning curves for junior scientists and support complex design work for seasoned chemists.
In my years advising both student and industry chemists, I’ve seen that the best research comes from sustained attention to quality—starting with molecules that behave as expected, batch after batch. While people outside the lab may overlook these day-to-day details, the experience-driven trust that grows around reliable compounds builds a foundation for breakthroughs. 3-Bromo-7-Fluoro-1H-Indazole is one such foundation stone.
No single product escapes market forces. Global events in recent years have shown how fragile supply chains can be—raw material shortages or border slowdowns cause headaches for research planners. The best suppliers of 3-Bromo-7-Fluoro-1H-Indazole publish detailed sourcing and production information. This transparency helps chemists make informed choices, selecting vendors who align with ethical sourcing and sustainability commitments.
Authenticity remains another concern. As with many specialty chemicals, unscrupulous actors sometimes offer substandard or counterfeit batches. Purchasing through well-vetted sources and demanding up-to-date analytical data helps safeguard research integrity. Peer-reviewed literature and independent lab verification protect against disappointment and wasted resources.
Chemical waste and sustainability are gaining spotlight attention, not just in regulatory corridors but also in daily operations. Practicing “green chemistry” means selecting intermediates that minimize environmental hazards and support efficient reaction conditions. 3-Bromo-7-Fluoro-1H-Indazole, with its halogen substitutions, naturally draws scrutiny. Thoughtful chemists look for ways to use catalytic amounts, streamline purification, and track waste disposal closely—this lowers environmental burdens while maintaining experimental rigor.
Improving research outcomes with 3-Bromo-7-Fluoro-1H-Indazole starts with knowledge-sharing. Documentation, peer review, and open access to robust protocols let everyone—whether in industrial or academic settings—learn from successes and setbacks. I’ve seen collaborations spark fresh insights and troubleshooting tips, moving entire projects forward after just a few shared emails or conference hallway conversations.
Greater access to high-quality chemical libraries at fair pricing extends opportunities to under-resourced labs. Group buying arrangements, nonprofit chemical repositories, or university consortia help smaller teams compete with larger firms. At the same time, educating newer chemists on the nuances of halogenated indazoles—understanding not only what works, but why certain methods succeed—expands the talent pool capable of turning raw compounds into real-world solutions.
Regulatory conversations also influence the future. Policymakers working hand-in-hand with researchers help ensure that environmental safety, labor rights, and transparency don’t fade into the background. Labs which voluntarily exceed minimum standards set the pace for safer, greener, and more reliable research cultures in turn.
Cutting-edge science often looks effortless in the pages of journals or at press announcements. Truthfully, it grows from months—sometimes years—of patient optimization, setbacks, and the steady refinement of both tools and techniques. My path, like so many others, has crossed with indazole chemistry time and again. The lessons learned stretch beyond reactions and yields; they touch on teamwork, persistence, and fair scrutiny of results.
One project with a related halogenated indazole came close to collapse after repeated purification issues. Only after reviewing methodical supplier notes and reaching out to peers did I discover that subtle batch impurities had crept in. Swapping to a carefully characterized 3-Bromo-7-Fluoro-1H-Indazole restored order, allowing the team’s optimization work to bear fruit. The shared experience reminded us all that the foundation of science rests on reproducibility, openness, and trust in one’s materials.
The science behind this compound isn’t flashy, but its consistency keeps the wheels of progress turning. Every new synthesis, every signal in a spectrum, and every follow-up experiment becomes a little smoother when built on a dependable intermediate. Setbacks and learning moments are inevitable, but they’re easier to manage with ingredients that meet the mark, time after time.
Trends in synthetic chemistry, drug discovery, and materials science all point toward growing demand for specialized, functionalized intermediates. Researchers are no longer content with “good enough”—they want strategic molecular features that speed up discovery and cut down on wasted effort. Compounds like 3-Bromo-7-Fluoro-1H-Indazole, with dual halogen sites, answer that call. Whether tweaking pharmacokinetics, chasing new modes of chemical reactivity, or perfecting molecular optoelectronics, these ingredients prove themselves again and again.
Continued investment in transparent supply, rigorous analytical standards, and sustainable practices matters more now than it did twenty years ago. As researchers build out their experimental platforms, collaborating across continents and sharing both data and struggles, the quiet reliability of this compound will keep unlocking new answers. I look forward to reading future reports—perhaps even seeing my former students publishing with this molecule—charting chemical territory that today, we can only imagine.
Choosing the right starting material has never mattered more to research efficiency or scientific progress. With 3-Bromo-7-Fluoro-1H-Indazole, labs set themselves up not just for quick wins, but for robust, lasting advances. Real progress grows from small steps, careful choices, and shared commitment. This compound, with its blend of stability and flexibility, fits comfortably into that picture.