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HS Code |
181775 |
| Chemical Name | 2-Bromo-4,5-Difluoroanisole |
| Molecular Formula | C7H5BrF2O |
| Molecular Weight | 223.02 |
| Cas Number | 1428786-74-8 |
| Appearance | Colorless to pale yellow liquid |
| Smiles | COC1=C(Br)C=C(F)C(=C1)F |
| Inchi | InChI=1S/C7H5BrF2O/c1-11-6-2-4(9)5(10)3-7(6)8/h2-3H,1H3 |
| Purity | Typically >97% |
| Solubility | Insoluble in water; soluble in organic solvents |
As an accredited 2-Bromo-4,5-Difluoroanisole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Packaged in a 25-gram amber glass bottle with a secure screw cap, labeled with product name, CAS number, and hazard symbols. |
| Shipping | 2-Bromo-4,5-Difluoroanisole is generally shipped in sealed, chemical-resistant containers, complying with regulatory standards. The packaging is designed to prevent leaks and exposure. It should be transported at room temperature, away from direct sunlight, heat, or incompatible materials. Ensure proper labeling and documentation according to local and international hazardous chemical regulations. |
| Storage | 2-Bromo-4,5-Difluoroanisole should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible materials such as strong oxidizing agents. Avoid exposure to moisture. Properly label the container and store it in a designated chemical storage cabinet, following all relevant safety and regulatory guidelines. |
Applications of 2-Bromo-4,5-Difluoroanisole in Industrial Manufacturing2-Bromo-4,5-Difluoroanisole plays a critical role across several specialized chemical manufacturing sectors. We detail specific industrial applications based on authentic downstream integration, compliance, and process routes, enabling end users to evaluate its fit for their formulations. 1. Pharmaceutical Intermediate SynthesisThis compound functions as an essential building block in the synthesis of advanced pharmaceutical intermediates, especially for active pharmaceutical ingredient (API) pipelines demanding highly selective halogen substitution. Medicinal chemistry groups use it for specific aryl ether introduction and step-growth reactions, optimizing molecular frameworks for anti-infective and oncology candidates. Its purity and traceability underpin qualification for regulated drug substance manufacturing, ensuring downstream compliance with global market requirements. Industry compliance standards
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2. Agrochemical Intermediate ProductionDownstream agrochemical manufacturers utilize 2-Bromo-4,5-Difluoroanisole to introduce a difluorosubstituted aromatic core in herbicide, fungicide, and insecticide active ingredients. Optimized fluorination and bromination improve bioactivity and product stability, especially for new-generation crop protection molecules. The material enables controlled structure-activity enhancements through reliable reactivity in both pilot and commercial plant settings. Industry compliance standards
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3. Advanced Material Monomer SourcingSpecialty polymer and liquid crystal manufacturers integrate this compound for its unique electron-withdrawing and steric properties. It contributes to high-performance polymers and specialty resins used in optoelectronic, dielectric, and high-value membrane applications. The raw material offers precise control of fluorine and bromine composition, supporting industry requirements for reproducible molecular weight and structural order. Industry compliance standards
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4. Fine Chemical & Specialty Dye ManufactureManufacturers of high-purity colorants and organic intermediates use this molecule for regioselective functionalization in synthesis of specialty dyes and pigments. It adds chemical stability and specific fluorescence or color-tuning properties required for advanced imaging, textile, and laser dye applications. Reliable supply and documentation support traceable batch processing for regulated colorant systems. Industry compliance standards
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Our plant turns out many halogenated aromatics, but few bring as much unique value as 2-Bromo-4,5-Difluoroanisole. Experienced chemical researchers often look for molecules with both reactivity and functional group tolerance, and this compound fits right into the needs of modern development. We have worked with this specialty anisole across pharmaceutical, agrochemical, and advanced material projects, and seen the real impact subtle structural changes can bring. This commentary draws directly from our years of hands-on production and client collaboration.
Chemists know that even minor variations in halogen placement change a compound’s personality. 2-Bromo-4,5-Difluoroanisole carries three substituents on the aromatic ring: a bromo group at the second position and two fluoro atoms at the fourth and fifth positions, with a methoxy anchoring it at position one. As a manufacturer, we focus on making sure the arrangement is exact — no misplaced bromine, no stray fluorinated isomers. Anything else, and the utility for syntheses drops quickly.
Purity is a top concern. For our batches, GC analysis routinely shows values above 98%. Even one percent contamination can throw a wrench into a year-long medicinal chemistry project. During recrystallization and distillation, we watch for color, odor, and trace impurities, because the product must meet the inflexible demands of both regulatory applications and research labs. You won’t find leftover halides, over-alkylated side products, or solvent residues in the specs we ship. Every lot carries a recorded melting point and a chromatogram trace.
Synthetic chemists always hunt for starting points that balance price and flexibility. 2-Bromo-4,5-Difluoroanisole stands out because the bromine handle reacts smoothly under mild cross-coupling conditions, which lets teams build complex scaffolds without running into decomposition or protecting-group headaches. The adjacent difluoro groups, on the other hand, tune the electron density so transformation selectivity is sharp — not too sluggish, not so reactive that byproducts dominate.
Few compounds offer this trio: functional halide, electronic modulation, and a methoxy for further functionalization. In our experience, project leaders come to us looking for ways to introduce both fluorine and methoxy groups at the right stage of a synthesis, without extra protection and deprotection. The benzene ring here opens doors for SNAr, Suzuki, Buchwald–Hartwig, and even nucleophilic methylation.
We have worked next to development chemists attempting routes with 2-bromo-3,5-difluoroanisole and even 2,4-difluorobromoanisole. They find those variants less predictable in coupling yields and regioselectivity, especially when building out larger structures for pharmaceutical candidates. Our 2-Bromo-4,5-Difluoroanisole has become the preferred option because the specific substitution pattern reduces the likelihood of unwanted side reactions during cross-coupling or substitution.
Compared to plain 2-bromoanisole, the difluoro substitution delivers improved stability to oxidative and thermal stress, vital in process scale-ups or when the route requires microwave or sealed-tube setups. The electron-poor ring deflects certain side-reactions and allows for a gentler hand during purification stages. We have run gram-to-kilogram transitions with minimal surprises, and that reliability is important when deadlines and pilot plant costs are real concerns.
Little molecules often have outsize impacts, especially ones that easily slot into multi-step synthetic plans. Our clients in agrochemical R&D tell us the difluoro anisole core slides perfectly into insecticides and fungicides, providing increased metabolic stability and improved leaf-surface adherence. The bromine offers a foothold for building more complex heterocycles, which is a route favored by many modern crop-protection advances.
Medicinal chemists see benefit, too. The difluoro motif brings metabolic resistance, making it a clever addition to lead optimization programs. With a bromine ready for palladium or copper-catalyzed substitutions, teams can quickly turn out libraries of new molecular variants for screening. Large pharma and biotech innovators are looking for alternatives to densely substituted aromatics that lack handling ease or generate more regulatory byproducts. In that environment, 2-Bromo-4,5-Difluoroanisole offers a low-boiling aromatic that keeps downstream processing simple.
Within materials science, our product gets picked for the synthesis of fluorinated monomers and specialty polymers. The anisole group supports compatibility in solvent systems and imparts non-stick or low-dielectric properties. Having the dependable supply direct from our reactors means project timelines don’t slip, and researchers don’t make trade-offs on purity or cost.
Many users want more than a reagent; they want a supply chain without regulatory nightmares. We run batch records and QA checks that track source materials, waste handling, and any contaminant trends across multiple campaigns. The final step purification often happens under reduced pressure, using custom column setups designed in-house, so we capture nearly all volatile organics before any venting step. By investing in tailored scrubbers and safe-waste protocols, we limit emissions well below national and EU standards.
Compared to legacy synthetic processes for brominated difluoroanisoles, our recent switch to less hazardous halogenating agents reduced both the time and energy footprint of each batch. Early on we ran multi-stage columns with more solvent and longer cycle times. Our latest campaigns leverage inline monitoring for both color and density, cutting down manual sampling and waste.
We’ve responded to the increased demand for documentation on traceability and sustainability. Full run history, including raw input origin, batch numbers, and analytics, are standard with every drum. Any requests for extra chromatograms or impurity profiles are met fast, because in our view transparency reduces risk for everyone in the chain.
Bulk buyers and lab researchers ask most about shelf life and transport. Our product stores securely at ambient temperature, as thorough moisture exclusion in final packaging stops hydrolysis and color change over long-term storage. No hidden stabilizers or problematic additives are used. As shippers, we have worked closely with most major carriers to ensure direct and timely delivery, and rely on feedback from both large industry and individual researchers to adjust pack sizes and shipping protocols as needed.
As a manufacturer, we have learned that seemingly minor details matter. Slight variations in transport or packaging can impact how well 2-Bromo-4,5-Difluoroanisole pours, dissolves, and disperses within process vessels. After one large pharma client struggled with caking issues, we revisited our drying procedure and type of liner. Now each drum leaves no chance for compaction or powder sticking to the walls, even after extended shelf storage or travel in variable climates.
Turning out consistent batches of a halogenated aromatic is never “routine.” Our operators have to work in a tightly controlled glove box environment for the early synthetic steps, due to the toxic and moisture-sensitive precursors. The bromo-fluoro functionalization step demands exacting temperature control — too high and the ring substitution starts producing positional isomers, too low and conversion drops. We have invested in programmable reactors that hold reaction windows to within a half degree and built in both IR and NMR monitoring for real-time verification.
Client feedback has played a big role in driving process tweaks. Over several years, we moved away from single-use reactors and improved both our cleaning regime and analytical sequencing. Both steps let us tighten impurity profiles and spot early any potential catalyst carryover or halide buildup. Regular plant audits by outside QC consultants catch blind spots and keep documentation practices at peak.
On the rare occasion a lot fails to meet release criteria, material is flag-marked and investigated at the root — not simply “repaired” by additional purification, because we have seen how side-products can evade some basic tests but create headaches in later cross-coupling reactions. As a manufacturer with direct oversight from batch to barrel, we believe in building trust by straight talk and open data with our end-users.
Some clients want 2-Bromo-4,5-Difluoroanisole in kilogram lots for early-stage screens. Others need larger volumes for API or active formulations. Our plant can swing between these needs because both the synthetic core and downstream handling have built-in scalability. Multi-lot requests are matched with reserved upstream input stocks, and rush jobs for gram-scale or sample-size shipments are routine. This flexibility comes from years of working with constantly shifting R&D schedules and urgent requests from both academic and industry scale projects.
We notice most scale-up failures begin with inconsistent input purity or batch-to-batch variation. Our solution stays simple: every single lot gets run through identical purification and analytics, regardless of order size or end application. A large global company receives the same batch as an early-career researcher — nothing set aside as “premium” versus “standard.” We reject the split-tier model because we know that shortcuts filter downstream quickly, undermining end product performance.
Across the industry, buyers compare 2-Bromo-4,5-Difluoroanisole with other regioisomers and halogen combinations. In interactive synthesis campaigns, the 4,5-difluoro pattern enables a sharper regioselectivity than variants with distant fluorine atoms. This pattern gives a clear route to further aromatic modifications by directed ortho-metalation or C–H activation. Colleagues requesting alternative halogens, such as iodinated or chlorinated anisoles, report less predictable downstream coupling efficiency or diminished stability under the same process conditions.
Cost differences often come up. Generic 2-bromoanisole is cheaper, but lacks the performance needed for tight SAR and drug metabolism studies. In our pilot scale experience, step-savings with our difluoro product often makes up for its slightly higher initial price. Cyclization, Suzuki, or SNAr transformations run with higher yield and fewer byproducts, with final outcomes that pass regulatory muster without extensive rework.
Demand continues to build for halogenated building blocks that deliver both process reliability and robust safety profiles. Our approach keeps evolving as client expectations and regulatory standards shift — not by theoretical discussion, but by regular review of operating records, plant maintenance logs, and user reports. Recent projects pushed us to add computer vision tools for better crystallization monitoring, making sure lot color and particle size stay within tightly prescribed bounds. It may seem a small detail, but both factors play a big part in ensuring high reactivity and no surprises on scale-up.
We support open channels for feedback and questions, answering at the technical level — IR spectra, impurity tables, or insight into specific synthetic modifications — without hiding behind boilerplate. Access to hands-on staff who have run the actual batches, not just sales teams, makes a difference for both routine purchases and special project support.
Supplying 2-Bromo-4,5-Difluoroanisole means aiming for both performance and dependability. We keep our raw material trends under continual review, making sure prices stay fair yet quality is never cut. Experience shows that the difluoro anisole core earns its place in advanced synthesis, from crop science to pharma, because it delivers what project chemists and process engineers need. We believe strong supply partnerships require evidence you can trust: open data, traceable lots, and direct technical engagement. The trust we build comes from consistent batches, honest answers, and a shared commitment to safe growth in modern chemistry.