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HS Code |
205816 |
| Product Name | 6-Fluoro-5-Bromoindole |
| Molecular Formula | C8H5BrFN |
| Molecular Weight | 230.04 g/mol |
| Cas Number | 885277-51-6 |
| Appearance | Off-white to pale yellow solid |
| Purity | Typically ≥ 97% |
| Solubility | Slightly soluble in organic solvents (e.g., DMSO, chloroform) |
| Smiles | Brc1ccc2[nH]ccc2c1F |
| Inchi | InChI=1S/C8H5BrFN/c9-6-2-3-8-7(10)1-4-11-8(6)5/h1-4,11H |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
As an accredited 6-Fluoro-5-Bromoindole 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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Indoles have shaped the field of organic chemistry for decades. Their structure sparks interest in those working across pharmaceuticals, agrochemicals, and advanced materials. Researchers look at these heterocycles for their broad reactive nature and their impact on bioactive compound development. Out of so many substituted indoles, 6-Fluoro-5-Bromoindole comes forward as a practical, potent choice when crafting new compounds. Plenty of stories in science start with a spark of curiosity—a new halogen or substitution that creates a ripple effect across research pipelines. I remember stumbling on substituted indoles during an undergraduate project, noticing how a minor tweak in structure could swing things from dull to dynamic when tracking synthetic pathways.
6-Fluoro-5-Bromoindole captures attention because of its unique two-halogen substitution. Instead of a plain indole ring, this model bears both a fluorine and a bromine on specific carbons. With the fluorine atom located at the six position and bromine at the five, this combination influences not only the reactivity of the molecule but also its physical and chemical properties. Each functional group brings something distinct. Fluorine’s tiny atomic radius and high electronegativity modify electron distribution, often increasing metabolic stability or binding affinity in potential drug candidates. Bromine, being bulkier and more polarizable, opens doors for further functionalization, particularly through selective cross-coupling reactions.
Research teams often look for building blocks that let them branch synthetic routes in multiple directions. 6-Fluoro-5-Bromoindole fits this requirement with its ability to undergo transformations at multiple positions. In my experience, having a compound like this on the shelf speeds up brainstorming and lab work for anyone working in medicinal chemistry.
Looking at physical aspects, 6-Fluoro-5-Bromoindole tends to appear as a pale solid at room temperature, common for small aromatic compounds in this series. Its melting point falls within a range that suits standard lab practices, so it can be weighed, transferred, and handled with ease. Solubility profile varies with solvent, but in many polar aprotic solvents, the compound readily dissolves, enabling a range of transformations from direct halogen exchange to metal-catalyzed coupling.
The dual-halogen motif brings particular analytical advantages too. Getting clean NMR spectra proves straightforward, as the fluorine and bromine each leave distinct “signatures” in spectral patterns. From a practical angle, this means fewer surprises when scaling up reactions or troubleshooting a series of complex steps. For chemists working late hours, that clarity in analysis can make or break a productive day in the lab.
In medicinal chemistry and process development, the ability to introduce or replace halogens with precision sets the path for novel structural analogs. With 6-Fluoro-5-Bromoindole, synthetic flexibility rises. The bromine atom allows for a range of coupling reactions—Suzuki, Stille, Heck, and more. Meanwhile, the fluorine atom presents a sort of “anchor,” influencing biological activity or resistance to enzymatic breakdown in target molecules.
These features matter when efficiency and yield are priorities. Sourcing a building block that shortens a synthetic route, increases selectivity, or cuts down on purification steps can have economic ripple effects. Many pharma researchers build “libraries” of analogs, and they rely on intermediates that can absorb or direct chemical attacks in controlled ways. In my time helping formulate screening campaigns, reliable building blocks meant fewer failed syntheses, reduced waste, and more actionable data for project leads.
Comparing this compound to unsubstituted indole, or even to mono-substituted versions, illustrates where subtle differences become game-changers. Laboratory procedures that work on simple indole often yield unpredictable results on brominated or fluorinated variants. Each substitution changes electron flow and alters where reactions happen. The presence of both halogens at these precise positions creates opportunities for sequential functionalization not possible on mono-substituted products.
The distinction grows sharper when comparing to other dihalogenated indoles. Changing position from five and six to five and seven, or from five and six to four and six, gives compounds with distinct reactivity and biological behavior. 6-Fluoro-5-Bromoindole becomes a useful “platform” molecule, especially for projects needing site-specific modifications or for teams exploring unique binding interactions in their targets.
In real-world lab settings, 6-Fluoro-5-Bromoindole finds use as a scaffold for building more complex molecules. Its two halogen handles give chemists an edge in introducing extra groups or directing reactivity at chosen sites. This makes it suitable for synthesizing small-molecule drug candidates, investigating enzyme inhibitors, or probing biological mechanisms.
In academic settings, many groups start with commercially available building blocks, and the reliability of 6-Fluoro-5-Bromoindole for standard transformations lends a lot of confidence. Chemists quickly find out which reagents cooperate with each halogen, optimizing conditions to control selectivity. It’s not just about hitting a yield target; it’s about building a pipeline where analog after analog can spring from a single trusted source. For teams facing publication deadlines, these workflow benefits mean faster time from concept to publishable results.
Time and resources describe the backbone of modern research, whether in academic or industrial labs. A thoughtfully substituted indole speeds up synthesis, minimizing the number of synthetic steps and reducing byproducts or waste streams. Efficiency also supports green chemistry goals, as shorter synthetic routes use fewer reagents and consume less energy.
Efficiency extends beyond cost and time. Substituted indoles—especially those with unique position halogen atoms—help generate structurally diverse compounds. In drug discovery, small changes in functional groups can flip pharmacological profiles from inactive to potent. Many recent papers cite fluorinated compounds for their enhanced metabolic profiles and bromines for their “handle” in C–C bond formation. Teams focused on sustainability also make conscious choices to cut down hazardous steps or use cleaner reagents, and well-designed intermediates fit into this philosophy.
Academic journals feature countless examples where halogenated indoles lay the groundwork for new active agents. Recent publications note that fluorine incorporation increases molecular metabolic stability, potentially reducing dosing frequency and improving side-effect profiles. Brominated indoles show their value as key intermediates in cross-coupling, giving rise to biphenyl derivatives and other complex motifs. Some studies highlight fluoro-bromo substitution as a strategy for late-stage diversification, allowing medicinal chemists to quickly fine-tune binding properties or enhance selectivity toward target receptors.
Scientists working in flavor and fragrance design, or in agrochemistry, also reach for substituted indoles to tweak volatility, hydrophobicity, or even UV stability. In each domain, structural variety creates a path to tailored functional molecules—forms that fit exacting needs in activity, reactivity, or environmental profile.
Even the most promising building blocks have hurdles. Sourcing high-purity intermediates sometimes slows projects, especially for unique substitutions like 6-Fluoro-5-Bromoindole. Reliable suppliers offering analytical data help labs avoid unpleasant surprises mid-synthesis. Prudent handling in the lab keeps yields high and ensures reproducibility.
Another challenge relates to downstream transformations. Not every halogenated indole responds the same way to classical reaction conditions. Sometimes, chemists adjust catalysts, bases, or temperatures to avoid unplanned side products. Over time, experience and published case studies help shape best practices, guiding those who are new to indole chemistry. Beginner chemists may feel intimidated by the complexity, but shared protocols and collective troubleshooting ease the learning curve.
For sustainability, process development teams constantly seek greener solvents, recyclable catalysts, or energy-saving heating methods as they scale reactions. Redesigning routes to leverage the reactivity of 6-Fluoro-5-Bromoindole streamlines many of these efforts.
A core strength when considering 6-Fluoro-5-Bromoindole comes from data-backed claims and experience shared in peer-reviewed research. Fluorine’s role in metabolic stability and bioactivity enhancement has strong support from journals like Journal of Medicinal Chemistry and Bioorganic & Medicinal Chemistry Letters. Bromine’s function as a coupling handle appears throughout process chemistry literature, shaping how new pharmaceuticals, agrochemicals, or material science products come to market.
Beyond literature, direct lab observation and project feedback reinforce practical benefit. Having used substituted indole building blocks myself when optimizing synthetic routes, the reliability of this compound shapes both planning and bench execution. Collaborating across departments, or even between academic and industrial partners, brings fresh insight into best practices. Collective experience, along with open data sharing, builds confidence in adopting new building blocks into screening libraries or production workflows.
Concrete improvements start by encouraging open dialogue between suppliers and research labs. Feedback loops matter—when labs flag issues in solubility, reactivity, or impurities, chemical suppliers can adjust synthesis or purification. This direct connection speeds up the process of bringing reliable materials to those who need them. Digital tracking of material provenance or certification also increases user confidence.
Improving synthetic protocols by sharing “tried and tested” conditions helps the wider community. Journals and online repositories now offer space for methods sections, troubleshooting notes, and supplementary data that earlier publications often overlooked. For those grappling with stubborn side reactions or low yields, tapping into these collective resources can save effort.
At the policy level, increased focus on green chemistry can incentivize industry to streamline their production of substituted indoles. Grants and regulatory nudges can tip the balance toward using less hazardous solvents, recyclable catalysts, or energy-efficient reactions. Such moves not only lower environmental impact but also cut operating costs for companies over time.
Looking ahead, advances in automation and AI-driven synthesis planning stand to further boost the value of versatile building blocks like 6-Fluoro-5-Bromoindole. As computer-assisted design becomes standard, access to well-characterized intermediates lets chemists realize virtual plans at the bench. In my own journey, watching older colleagues hand-scribe reaction schemes and comparing that to today’s predictive software makes it clear—the blend of solid building blocks with digital innovation defines future breakthroughs.
Education and outreach also play a role. Training students in practical organic chemistry with “real-world” building blocks sharpens their skills and readies them for industry. Interdisciplinary projects linking chemistry to biology or materials science often trace their success to having the right intermediate at just the right time. Supporting access, documentation, and cross-disciplinary networks ensures that innovations from one lab quickly scale to benefit many.
The real story of 6-Fluoro-5-Bromoindole is about meshing structure, reactivity, and utility into a single, versatile tool. Its two-halogen frame lets chemists reach farther, fine-tune more precisely, and cut waste, time, and cost in the lab. Whether driving a medicinal chemistry campaign, fueling a process development push, or advancing academic curiosity, this compound opens the door to next-generation discovery. In my experience, the right building block at the right moment not only solves today’s problems but also inspires tomorrow’s answers.