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HS Code |
894424 |
| Chemical Name | 2,3-Difluoro-4-Bromonitrobenzene |
| Molecular Formula | C6H2BrF2NO2 |
| Molecular Weight | 238.99 g/mol |
| Cas Number | 60050-46-6 |
| Appearance | Pale yellow to light brown solid |
| Melting Point | 52-56°C |
| Density | 1.89 g/cm3 (estimated) |
| Solubility | Slightly soluble in common organic solvents |
| Smiles | C1=CC(=C(C(=C1Br)[N+](=O)[O-])F)F |
| Inchi | InChI=1S/C6H2BrF2NO2/c7-3-1-4(8)6(9(11)12)2-5(3)10/h1-2H |
| Storage Conditions | Store in cool, dry, well-ventilated area |
As an accredited 2,3-Difluoro-4-Bromonitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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Chemists working on complex challenges often reach for specialty compounds that don’t always make the headlines. 2,3-Difluoro-4-Bromonitrobenzene stands out as one of those chemicals that proves its worth in quiet but critical ways during the research and development of pharmaceuticals and other advanced materials.
Its molecular structure includes two fluorine atoms at the 2 and 3 positions, a bromine at the 4 position, and a nitro group, all attached to a benzene ring. At first glance, the name might seem overwhelming to anyone outside organic chemistry, but every piece of this molecule brings something to the table.
Plenty of substituted nitrobenzenes are available for synthesis work, but not many offer the carefully balanced features that this compound provides. Fluorine atoms bring both chemical stability and reactivity, depending on what the synthesis requires. The bromine offers a convenient handle for further functionalization through palladium-catalyzed coupling or similar reactions. In contrast with simpler nitrobenzenes or mono-halogenated alternatives, this molecule carries a much richer reactivity profile. Chemists get more options, fewer unwanted by-products, and access to molecules that previously seemed out of reach.
As someone who spent years tackling structure-activity relationships, I know the importance of precise substitution around a benzene ring. Changing the type or position of a halogen atom may mean the difference between an active drug candidate and a mediocre one. The 2,3-difluoro pattern on this molecule often helps with fine-tuning properties like metabolic stability, permeability, or binding characteristics for pharmaceutical leads.
Substituents like bromine and nitro groups don’t just exist for show. The nitro group serves as a reactive site for further reduction, substitution, or other transformations, while bromine’s presence creates pathways to more specialized derivatives using cross-coupling techniques. Many researchers find that the combined electron-withdrawing effects of fluorine and nitro make the aromatic system uniquely reactive, so reactions proceed with a level of control and selectivity that’s hard to match.
Sourcing 2,3-Difluoro-4-Bromonitrobenzene with high purity ensures predictable results in synthesis. Toxic or inconsistent batches aren’t just academic headaches—they slow down entire research pipelines and add uncertainty to critical preclinical projects. The compound generally arrives as a crystalline solid, with precise melting points and careful quality checks to minimize any side reactions during use. In my experience, reputable suppliers can provide analytical data confirming structure, including proton and fluorine NMR, IR spectra, and HPLC purity. Skimping on quality leads to wasted time cleaning up mixtures or troubleshooting failed reactions that should have worked.
Researchers investigating new chemical entities or process optimizations in agrochemicals and pharmaceuticals frequently turn to compounds like this. I remember a project where a similar difluorinated aromatic sped us past a synthetic bottleneck; without those subtle electronic tweaks provided by the fluorine atoms, the desired coupling never took off. The bromine in the 4 position opens up the Suzuki-Miyaura and Buchwald-Hartwig reactions—workhorse transformations in drug discovery that let teams assemble libraries of tailored molecules fast.
Another key advantage shows up in protected intermediate synthesis. The nitro group is more than a placeholder: it can be reduced to an amine as needed, or swapped out under tough conditions that would fry other groups. Flexibility in downstream processing remains crucial as chemists bounce between different synthetic strategies for yield, purity, and scale-up.
Safety always mingles with excitement when dealing with halo-nitrobenzenes. While this compound isn’t as volatile or hazardous as some of its wilder cousins, risk assessments should factor into daily lab work. Proper ventilation and personal protective equipment keep researchers safe—lessons hard-learned from my earliest days in pharmaceutical chemistry. I’ve seen what happens if glove protocols are ignored or if proper waste procedures slip, demonstrating just how important lab discipline remains.
There’s also an environmental angle. Fluorinated chemicals can persist and bioaccumulate, so responsible sourcing and disposal matter. Teams with solid waste protocols make all the difference in keeping both people and the planet in good shape for future research.
Browsing any chemical supplier’s catalogue, I notice dozens of nitrobenzenes with halogens at various positions. Most of them don’t offer the double fluorine plus bromine pattern seen here. The unique mix of two adjacent fluorines creates a distinct electron-deficient profile, which shifts the reactivity compared to single-halogen or mixed-halogen derivatives. For synthetic chemists, this pattern translates to new reaction pathways or improved yields, especially when working with difficult aromatic substitutions.
Single-fluorinated nitrobenzenes offer less capacity for tuning physical and chemical properties. Compounds with bromine alone rarely enable the same breadth of downstream transformations. Upgrading to this difluorinated bromonitrobenzene gives research teams extra leverage: controlling polarity, increasing biological activity, or optimizing process safety. I’ve seen medicinal chemistry teams rescue an otherwise unpromising series by swapping in a difluoro functionality, unlocking activity in previously flat results.
Running reactions with 2,3-Difluoro-4-Bromonitrobenzene isn’t without its hurdles. Solubility sometimes throws a wrench into otherwise simple protocols, especially in greener solvents. It helps to approach each new reaction with a mindset open to tweaks—small changes to stirring, heating, or dilution have paid off far more than forcing high-throughput strategies. The limited commercial availability of the compound at kilogram scale may slow industrial process development, but for most discovery projects, the research grade suffices.
In pilot plant trials, waste management pops up as a persistent concern. Halogenated waste streams demand specialized handling, and these realities now shape how teams design their reaction workflows. Chemists aiming for sustainable processes look for ways to minimize halogen release or recover valuable materials rather than disposing of them.
Modern medicinal chemistry leans on compounds like 2,3-Difluoro-4-Bromonitrobenzene to build complexity in fewer steps. The market’s push for rapid prototype molecules, especially in oncology and antiviral research, raises the value of precursors that allow efficient late-stage diversification. I spent plenty of late nights testing parallel reactions, swapping out halogens and watching activity profiles shift. Consistent access to advanced intermediates such as this one can mean the difference between a stalled pipeline and a promising lead entering animal studies.
For researchers working with fragment-based drug design, the ability to snap together fragments with pre-configured functional groups—like those present here—means shorter paths to results and more room for SAR exploration. This compound serves as both a building block and a bridge between simple and complex targets, streamlining the journey from benchtop to application.
Feedback from development labs consistently highlights this compound’s reliability in challenging transformations. One industrial chemist noted that attempts to introduce fluorine atoms late in a synthesis struggled with yields and purity, leading the team to shift strategies. Starting with a difluorinated benzene, especially in a system with a reactive bromine, saved weeks of optimization. Another team leveraged the electron-withdrawing effect of both nitro and fluorine groups to steer selectivity in aromatic substitution, achieving results that would have required elaborate protecting group strategies using standard nitrobenzenes.
Projects aimed at exploring bioisosteric replacements similarly benefitted from the specific arrangement found in this compound. In a few cases, the nitro group proved more robust against reduction than predicted, giving rise to unexpected new transformation opportunities after consultation with experienced synthetic chemists. Those field stories underline that each substitution pattern isn’t just a matter of numbers—it’s a collection of possibilities that only unlock with repeated use, careful study, and open collaboration across teams.
As debates about sustainability reach into every lab, the way chemists use halogenated and nitro-substituted aromatics faces more scrutiny. Experienced teams know that planned reaction routes and waste minimization make all the difference. Using building blocks like 2,3-Difluoro-4-Bromonitrobenzene with forethought—recycling solvents, neutralizing hazardous intermediates quickly, opting for catalytic over stoichiometric reagents—encourages safer and less wasteful practices that still deliver the performance research demands.
Through trial, error, and open conversation, groups share ways to rework protocols, lowering energy demands or reducing the amount of supporting reagents. The move from classical halogenated solvents to more environmentally sound alternatives shows that adaptation doesn’t always mean compromise. It often means discovering new efficiencies, saving time and money, while still producing first-class results.
Any synthetic chemist has tales of lost days and failed reactions due to off-spec or misidentified intermediates. Over the years, sourcing 2,3-Difluoro-4-Bromonitrobenzene from trusted suppliers became just as important as a clever reaction plan. Data transparency lies at the core of confidence: full spectral data, certificates of analysis, and a willingness to troubleshoot any batch discrepancies set apart the partners you return to. I’ve seen collaboration between chemists and suppliers spark small changes—extra TLC in purification or just-in-time logistics—that ripple through project timelines.
Reliability isn’t just about product quality; it’s about keeping lines of communication open when timelines slip or requirements change. The research community works best when knowledge, not just materials, flows freely.
As research pivots toward ever more demanding targets—from new-generation antibiotics to targeted enzyme inhibitors—the molecular structure of 2,3-Difluoro-4-Bromonitrobenzene puts it at the forefront of innovation. I notice an uptick in publications citing difluoro-bromonitro frameworks as key intermediates in both academic and industrial research, highlighting their versatility.
Emerging applications include small-molecule fluorescent probes, functionalized agrochemicals with enhanced stability, and advanced materials for electronics. The electron-rich-to-poor tuning possible with this compound, paired with the modular connection points for further elaboration, drives continued demand. The science moves quickly, but chemical building blocks like this anchor new ideas in practical, achievable goals.
Much of the expertise in working with complex intermediates like this one comes through apprenticeship and peer exchange. Workshops, technical notes, and honest reports of failed attempts build a culture of safety and innovation. My own learning curve included as many mistakes as successes, and advice from a more experienced colleague spared me plenty of repeat errors handling sensitive nitrobenzenes. Written guides focused on real-world troubleshooting—how to scale up safely, what to expect from work-ups, alternative purification paths—help teams get the most from each gram of starting material.
Online communities, forums, and open-access journals now extend this support beyond the walls of the research institution. I often see posts comparing two or three difluoro-nitrobenzenes in parallel, trading tips on which coupling strategies outperform the rest and sharing results with detailed procedural notes.
Challenges linked to this molecule center on the expected pain points for halogenated nitroaromatics: solubility, side reactions, and purification. To address these, seasoned chemists recommend slight increases in reaction temperature, fine tuning solvent polarity, or adopting microwave-accelerated conditions when standard methods lag behind. Specific work-up protocols and strategies—like in-situ reduction of the nitro group to capture intermediate products—reduce risk and improve reproducibility.
In one project, a tricky purification became manageable by choosing reverse-phase chromatography instead of traditional silica, a change that not only increased yield but also saved time downstream. Insights like these don’t always appear in formal literature but make all the difference for teams under real-world pressure to deliver.
In an era where speed, efficiency, and safety define chemical innovation, this advanced aromatic compound meets researchers’ evolving needs. Whether preparing intricate small-molecule scaffolds or pushing into uncharted chemical territories, the features built into this molecule—strategically placed fluorines, a bromine for cross-coupling, and a versatile nitro group—continue to unlock new synthetic and practical opportunities.
Conversations with colleagues confirm its value again and again: the right tool at the right stage can transform a project. For all the new reagents entering the field, the reliability and adaptability of 2,3-Difluoro-4-Bromonitrobenzene secure its place in the toolkit of forward-thinking chemists poised to tackle tomorrow’s challenges.