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HS Code |
797616 |
| Productname | 5-Bromo-8-Fluoroquinoline |
| Casnumber | 882864-73-7 |
| Molecularformula | C9H4BrFN |
| Molecularweight | 226.04 |
| Appearance | Off-white to light yellow solid |
| Meltingpoint | 69-73°C |
| Purity | Typically >98% |
| Smiles | Brc1ccc2ccnc(F)c2c1 |
| Boilingpoint | 327.5°C at 760 mmHg |
| Density | 1.707 g/cm3 |
| Solubility | Soluble in DMSO, slightly soluble in water |
| Storageconditions | Store at room temperature, keep container tightly closed |
As an accredited 5-Bromo-8-Fluoroquinoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | |
| Shipping | |
| Storage |
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In recent years, 5-Bromo-8-Fluoroquinoline has gained a reputation among research professionals who know their way around a reaction setup. There’s always something interesting about a compound that manages to stand out in a crowded field, especially one like quinoline derivatives, where small modifications impact big projects. The presence of both a bromine atom at the 5-position and a fluorine at the 8-position on the quinoline ring gives this molecule distinct character, making it a reliable choice for those working on pharmaceutical intermediates, diagnostic markers, or complex organic frameworks.
From experience and industry discussions, professionals appreciate the purity and stability of high-grade 5-Bromo-8-Fluoroquinoline in solid or crystalline form. A typical batch flows as an off-white to light yellow powder, holding up well over time, which cuts down on worries over quick degradation. With a reliable melting point, researchers skip the uncertainty and focus on results. There’s a sense of confidence in weighing out this compound, measuring to the milligram, knowing the lot matches published spectra or HPLC standards. It’s easy to underestimate the value of reproducibility until trial-and-error, solvents, and time start to run thin in the lab.
This compound often finds a spot as a starting material or a key intermediate in the synthesis of more elaborate molecules. Medicinal chemists actively seek out bromo-fluoro analogs as scaffolds, looking for that nudge in activity or selectivity during lead optimization. Because the quinoline core frequently appears in anti-infectives, kinase inhibitors, and imaging agents, any modification that’s easy to introduce and opens doors to unique transformations gets close attention. The presence of bromine at the 5-position allows for Suzuki-Miyaura, Buchwald-Hartwig, or other palladium-catalyzed couplings, making this compound convenient for linking up a range of functional groups. The fluorine at the 8-position doesn’t just nudge the electronic properties – it can fine-tune drug-like behavior, metabolic stability, and binding affinity, something both bench scientists and computational chemists value.
Anecdotes from project teams suggest that starting with 5-Bromo-8-Fluoroquinoline often helps sidestep some classic challenges. Take the difficulty of introducing a halogen and a fluorine on the quinoline ring in one pot, for example. Some routes burn up time and budget, but commercially available, characterized product lets teams move beyond the hurdles and focus on late-stage functionalization. On a personal note, a reliable intermediate that doesn’t introduce its own set of variables becomes a small relief on projects with tight deadlines. There’s always another step to optimize or another analog to chase, but having the building blocks under control keeps things predictable.
The market offers a range of halogenated quinolines and related aza-heterocycles, but few combinations balance reactivity, stability, and versatility like 5-Bromo-8-Fluoroquinoline. Compare it with, say, 5-Chloro-8-Fluoroquinoline. The switch from bromine to chlorine changes the coupling reactivity, sometimes leading to lower yields in cross-coupling steps. Switching the position of the fluorine often alters selectivity in downstream reactions. Some analogs with multiple halogens at other positions risk extra deactivation or unwanted side reactions, especially when scaling up. In contrast, the distinct substitution pattern in 5-Bromo-8-Fluoroquinoline usually offers enough of a synthetic handle for most coupling protocols without overcomplicating purification.
Other options like 8-Fluoroquinoline alone frequently fall short on reactivity when further functionalization is needed. A simple bromoquinoline might miss the push in biological activity that fluorine sometimes brings. The synergy of both substituents unlocks more choices – a point like this doesn’t always appear on spec sheets but tends to show up in results from screening campaigns and SAR tables. Synthetic chemists facing an endless flow of project demands don’t have the patience for uncooperative building blocks. Picking a molecule that consistently integrates in multi-step routes pays off in labor saved and surprises avoided.
Standing at the interface between R&D and production, consistency matters more than many care to admit. Over several years, the labs I’ve worked with have handled batches of quinoline derivatives from many sources. Not every supplier delivers on their claims, especially in a field where upfront costs often tempt buyers to cut corners. With high-purity 5-Bromo-8-Fluoroquinoline, you see the value each time the NMR matches, the TLC spot migrates as expected, and the product behaves through several synthetic steps. Such reliability frees up hours otherwise spent troubleshooting or hunting down invisible contaminants. The literature backs this up too – peer-reviewed work on library synthesis and small molecule programs frequently notes the role of building block quality in success or failure.
It’s not just about the raw numbers on a certificate of analysis. Real-world use throws curveballs: reactions go off-schedule, solvents mutate your timelines, dried product gets sticky if not stored right. Through repeated use, 5-Bromo-8-Fluoroquinoline has shown a knack for weathering variable storage, travel, and even occasional temperature abuse. Nobody wants to admit to a bag left out overnight, but the best chemical stocks handle minor human error. Over time, this resilience saves money—not by being the nominally cheapest, but by cutting rework, failed reactions, and last-minute shipments.
People who spend hours in the lab grow to respect molecules that deliver their promise without adding extra safety headaches. 5-Bromo-8-Fluoroquinoline holds up in standard lab storage: cool, dry, and away from strong oxidizers or acids. It doesn’t fume, polymerize, or let off suspect odors. Standard nitrile gloves, goggles, and working in a well-ventilated hood meet responsible use. Reports from colleagues show few outliers – if handled according to good laboratory practices, this molecule rarely causes trouble. Of course, as with all halogenated aromatics, keeping it off skin and out of waste streams makes sense, but the practical risks line up with those of similar quinoline compounds. There’s value in minimizing surprises, especially in settings where less experienced researchers join the team or automation manages repetitive steps.
Across the industry, regulatory compliance and waste management rules put extra pressure on users to know what sits on their shelves. 5-Bromo-8-Fluoroquinoline’s straightforward hazard profile allows labs to integrate it into workflow without jumping through too many hoops. This doesn’t just smooth day-to-day work; it builds trust across teams that the toolbox holds what they expect, not unwelcome surprises.
There’s a difference between a “commodity” intermediate and a true workhorse. Over a decade in labs—academic and industrial—I’ve watched the same handful of reliable intermediates drive dozens of exploratory projects. 5-Bromo-8-Fluoroquinoline fits that bill. Its core value emerges in multistep routes, where features like selective coupling or electronic tuning save an entire week, sometimes more. Teams running SAR series for anticancer targets, or searching for better imaging agents in diagnostics, circle back to this compound because of its versatility and predictable behavior. It’s a little like having a favorite wrench in the toolbox—once a chemist finds it useful, it keeps showing up in future plans.
Peer-reviewed studies back this experience: articles focused on optimizing biosynthetic pathways or analog libraries often list bromo-fluoroquinolines as key starting points. Recent advances in C–N and C–C bond formation highlight how the bromine substituent creates a reliable anchor for further transformations, giving medicinal chemistry programs more agility. The 8-fluorine, for its part, has emerged as a fine-tuning tool for metabolic stability, especially in drug optimization campaigns trying to push molecules over the “oral bioavailability” hump. Such traits place 5-Bromo-8-Fluoroquinoline at an interesting intersection of synthetic convenience and biological promise.
The uptick in demand for specialty chemicals like halogenated quinolines reflects both evolving research needs and the push for faster lead development. At the same time, global events put extra pressure on the chemistry supply chain. COVID-era shortages forced many labs to rethink their reliance on single suppliers, and recurring disruptions haven’t disappeared. With intermediates like 5-Bromo-8-Fluoroquinoline, availability, traceability, and batch consistency stand out as serious decision factors. Some researchers have shifted toward stocking larger quantities, even pooling orders across labs or institutions. Having a well-documented material history, including batch origin and route of synthesis, gets more attention these days, especially when scalability comes into play or regulatory questions arise.
Practical solutions grow from experience: network with trusted peers, vet new suppliers with a trial batch, and keep backup options in play. A few organizations have worked to develop in-house synthesis protocols for key building blocks, including 5-Bromo-8-Fluoroquinoline, as a hedge against shortages. Open communication across purchasing, safety, and chemistry teams turns out to save more headaches than focusing only on price. Sharing information on supplier quality and shipping reliability with colleagues shortens the learning curve and can help catch subtle differences in product quality before they impact a full-scale project.
Innovation relies not only on brilliant minds and resources but also on reliable materials. Building blocks like 5-Bromo-8-Fluoroquinoline make it possible to move quickly from idea to prototype—the sort of progress that powers both academic exploration and commercial patents. In conversations with researchers working at the interface of chemistry and biology, the best experiences often stem from smooth-running syntheses, not just clever target design. Every time a material shows up, unpacks with minimal fuss, and slots right into the planned route, chemists take notice. Such experiences accumulate into best practices and influence future choices.
For younger scientists, an easy-to-work-with building block allows more time to focus on what matters: learning core concepts, troubleshooting real problems, and thinking creatively about new molecular architectures. For managers and project leaders, products that deliver as promised save energy otherwise spent on damage control. The value, then, lies not just in physical purity or price per gram, but in supporting the people working behind the bench. Where research and development budgets stretch thin, choosing compounds that deliver predictable results has direct impact on timelines, morale, and team success.
Navigating a shelf lined with dozens of quinoline derivatives, discerning scientists gravitate toward repeatable performance and proven value. In the past, I’ve watched project teams pick 5-Bromo-8-Fluoroquinoline not because it looks the fanciest on a catalog page, but because its features—optimal reactivity, reasonable shelf life, and usefulness in many downstream reactions—come proven by word of mouth and peer-reviewed projects alike. Few factors shape loyalty like repeated good experiences, especially on a hard deadline or when synthesizing sensitive analogs late in a drug discovery program.
There’s pressure in every research environment to chase the next big breakthrough, but real progress often comes down to a handful of well-chosen reagents that remove as many unknowns as possible. In a competitive market for fine chemicals and research intermediates, products that actually stand out for their impact, not just unique features, gain traction and win repeat customers. The balance achieved in 5-Bromo-8-Fluoroquinoline—combining practical coupling reactivity, stability, and straightforward storage—makes it memorable for professionals who have seen promising projects derailed by less reliable materials.
Responsible stewardship in research means more than just safe handling or regulatory compliance; it means using materials that support efficient, thoughtful science. 5-Bromo-8-Fluoroquinoline gives teams a solid foundation to build on, whether in small startups or large institutions. Its consistent supply and honest presentation make it a model for what modern research supplies should offer—clear specifications, batch traceability, and practical performance supported by real-world use. In discussions with colleagues, the value of this approach echoes through successful programs: deliver reliability at the molecular level, and the rest follows.
Even as automation grows and digital tracking tools gain ground, there’s still no substitute for honest, robust chemical building blocks. Each lot, every order, reflects a commitment to research integrity. Choosing wisely not only avoids delays but supports the wider push for transparency, reproducibility, and sustainable growth in science. The industry as a whole benefits from raising the bar for intermediate quality, and building blocks like 5-Bromo-8-Fluoroquinoline continue to help push those standards higher.
Researchers in chemistry, materials science, and drug development want products and partners they can count on. While there’s no single answer to every synthetic challenge, many projects benefit from consistent, thoughtfully designed intermediates. 5-Bromo-8-Fluoroquinoline stands at the intersection of synthetic flexibility and practical reliability, meeting the demands of today’s research agendas. Readers thinking about project design or troubleshooting ongoing routes should take a closer look at how this compound fits project needs, keeps workflows moving smoothly, and supports the drive for innovation.
If decades of work at the bench have shown anything, it’s this: the path to discovery rarely runs straight, but the journey improves with the right tools. Products like 5-Bromo-8-Fluoroquinoline, built for the demands of real research, bridge the gap between challenge and progress, helping teams turn molecular ideas into reality without unnecessary complications. That trust, earned through repeated success, is hard to beat.