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HS Code |
753968 |
| Productname | 2-Amino-2'-Fluoro-5-Bromobenzophenone |
| Molecularformula | C13H9BrFNO |
| Molecularweight | 294.12 g/mol |
| Casnumber | 1186125-53-0 |
| Appearance | Solid |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=CC=C1C(=O)C2=CC(=C(C=C2)Br)N)F |
| Solubility | DMSO, DMF, limited in water |
| Storageconditions | Store at 2-8°C, protected from light |
| Synonyms | 5-Bromo-2'-fluoro-2-aminobenzophenone |
As an accredited 2-Amino-2'-Fluoro-5-Bromobenzophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, screw cap, 10 grams, labeled with product name, CAS number, hazard symbols, supplier info, and storage instructions. |
| Shipping | 2-Amino-2'-Fluoro-5-Bromobenzophenone is shipped in secure, airtight containers to prevent contamination and degradation. Packaging complies with chemical transport regulations, ensuring safety during transit. The chemical is labeled with appropriate hazard and handling information and is shipped via certified carriers with tracking to guarantee prompt and safe delivery. |
| Storage | 2-Amino-2'-Fluoro-5-Bromobenzophenone should be stored in a tightly sealed container, away from direct sunlight and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature. Separate from strong oxidizers, acids, and bases. Always label the container clearly and ensure proper chemical handling procedures are followed, including using appropriate personal protective equipment (PPE). |
Applications of 2-Amino-2'-Fluoro-5-Bromobenzophenone in Industrial Manufacturing2-Amino-2'-Fluoro-5-Bromobenzophenone is a specialized intermediate widely adopted across multiple segments within the pharmaceutical, agrochemical, and specialty chemical industries. As a direct producer, we supply this compound with a strict focus on meeting complex downstream process needs and ensuring adherence to global compliance protocols. The following scenarios reflect established industrial avenues utilizing this material, covering integration into key synthesis processes and compliance with specific regulatory frameworks. 1. Active Pharmaceutical Ingredient (API) Synthesis: Fluorinated Aromatic IntermediatesThis compound serves as a core building block in the manufacture of certain fluorinated APIs, particularly within the non-steroidal anti-inflammatory drugs (NSAIDs) and selective kinase inhibitor classes. Its structure introduces both halogen and amine functionality, essential for subsequent coupling and cyclization reactions performed in designated GMP cleanrooms. Pharmaceutical manufacturers rely on this intermediate for batch production under validated reaction conditions to achieve strict impurity profiles and final active content specifications. Industry compliance standards
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2. Agrochemical Synthesis: Herbicide and Pesticide IntermediateDownstream agrochemical manufacturers use this molecule within regulated synthetic routes for certain modern herbicides and fungicides where substitution patterns enable enhanced target selectivity and environmental persistence. The raw material is processed in controlled reactors for coupling and derivatization, where accurate dosing ensures minimized byproduct formation and consistent product bioavailability. Industry compliance standards
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3. Specialty Dye Intermediate for Colorants in ElectronicsThis specialty intermediate acts as a key precursor in the production of certain high-performance dyes required for organic light-emitting diodes (OLEDs) and laser printing inks. The fluoro and bromo functionalities enhance photostability and enable site-selective polymerization, crucial for thin-film applications where dye migration or degradation undermines reliability. Integration occurs in specialized pigment synthesis workshops where precise batch control and trace metal analysis are standard. Industry compliance standards
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4. Intermediate for Liquid Crystal Material ProductionManufacturers of advanced liquid crystal displays (LCDs) utilize this compound as a precursor for synthesizing mesogenic molecules. Halogenated benzophenones like this one impart improved anisotropy and controlled refractive properties. Production lines implement contamination control and specific temperature tracking to preserve the functional group integrity needed for downstream high-purity split-phase distillation and fractionation. Industry compliance standards
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5. Polymer Crosslinking Agent for Engineering PlasticsThis compound is also introduced as a functional additive in the development of halogen-functionalized engineering polymers, including aryl polyamides and copolyesters. The unique halogen and amine arrangement provides active binding sites for crosslinking or post-polymerization modification, delivering mechanical reinforcement without compromising transparency or thermal stability. Producers employ closed-system compounding and extrusion lines for consistent material incorporation and worker safety. Industry compliance standards
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We know the value of every step in organic synthesis, especially in the pharmaceutical sector where precision and purity create the foundation for active pharmaceutical ingredient (API) development. In this context, 2-Amino-2'-Fluoro-5-Bromobenzophenone has emerged as an indispensable intermediate thanks to its distinct structural features and performance during downstream processing. We have invested years in refining both our production process and quality controls for this compound, recognizing the necessity for consistent supply and dependable specification in any high-throughput laboratory or commercial plant.
Our regular engagement with innovative drug discovery teams has highlighted that minor differences in substituents and molecular orientation can transform an entire route’s success. In this case, the electron-withdrawing fluoro group and the ortho bromine atom create new possibilities for selectivity or reactivity. The amino group unlocks sites for further modifications, giving chemists room to maneuver in areas like kinase inhibitor development, antiviral candidates, and other heterocycle syntheses. Through direct discussions with research chemists, these properties have been shown repeatedly to boost both yield and purity in next-step reactions versus more basic benzophenone analogs.
We typically manufacture 2-Amino-2'-Fluoro-5-Bromobenzophenone as a crystalline solid with purity levels above 98% as determined by HPLC and NMR. Our production lines have been calibrated to maintain narrow tolerances, reducing impurities like residual halides that might cause downstream complications. Each batch undergoes both spectroscopic verification and physical observation, because we have learned that small changes in handling conditions—moisture uptake, storage temperatures, or particle size during milling—impact downstream reproducibility. We do not treat these checks as “extras,” but as necessary checkpoints that align with the expectations of R&D teams dealing with challenging syntheses.
Our hands-on experience has taught us that minor tweaks to a molecule’s structure, such as positioning amino, fluoro, or bromo groups, allow researchers to tailor key reaction profiles. Specifically, the introduction of a fluoro atom adjacent to the benzophenone core alters electronic characteristics and facilitates Suzuki, Buchwald–Hartwig, and Ullmann reactions. The bromo position offers reliable reactivity for cross-coupling and nucleophilic substitution under both classic and microwave-assisted protocols. Combined with the ortho-amino group, the result is an intermediate more effective than simple halogenated or aminated benzophenones. Labs working on structure–activity relationship studies or building libraries for high-throughput screening have often pointed out the difference in success rates when subtle electronic effects are leveraged.
We manufacture this compound at scale using a multi-step synthetic route, tightly controlling parameters such as temperature gradients and reagent addition rates. In scaling up from bench to pilot to full commercial quantities, we confronted challenges like overcoming byproduct formation and maintaining sharp product isolation phases. Our workforce has learned through real cycles—yield losses from inadequate agitation, bottlenecks from non-optimal solvent selection, purity slips from incomplete phase separation. By adapting our processes, using closed-loop analytics, and scheduling regular blind testing, we built more trust with clients. Researchers from fast-moving biotech startups and global pharmaceutical firms alike have responded positively, as batch-to-batch variation often halts critical programs.
Often, project leads ask us how this product stands against similar intermediates or unadorned benzophenones. The addition of fluorine offers increased metabolic stability in final compounds—a detail picked up in numerous studies probing oxidative metabolism. The bromine atom allows for highly specific palladium-catalyzed couplings where reliability is paramount. Labs aiming for higher substitution efficiency or investigating SAR in fluorinated arenas skip the base benzophenone and opt for this intermediate because it provides a platform free from uncontrolled side reactions. These attributes become apparent only through extended synthetic cycles; side-by-side projects reveal marked differences in overall efficiency, purification time, and byproduct suppression—results our technical partners have documented and shared back to us, improving our understanding and processes.
Waste minimization remains a cornerstone of responsible chemical manufacturing. Our facility includes solvent recycling units and closed-system waste collection points, informed by benchmarking against green chemistry principles. While 2-Amino-2'-Fluoro-5-Bromobenzophenone itself is not an end-use product, waste stream treatment affects resource allocation and time to delivery. Each kilogram produced means controlled purification stages, reduced ionic contamination, and simplified crystallization cycles, leading in turn to more efficient use of lab and plant resources. Many of our downstream partners have noted that high-purity input materials cut both costs and clean-up obligations, freeing both people and budget for core research. Lessons from inefficient downstream isolations in client feedback loops have driven continued improvement in our own waste reduction protocols.
Critical discussions with logistics specialists and end users have convinced us of one truth: packaging and shipping become as significant as synthesis quality itself. This product ships in glass or high-density polyethylene containers, sealed under nitrogen to prevent unwanted degradation. The subtle difference this makes is clear on the receiving end—no delayed project timelines due to compromised intermediate, and an immediate go-ahead for compound library expansion. Researchers facing tight windows for project milestones can rely on predictable, fresh material. The importance of climate-controlled storage, including temperature and humidity monitoring, came directly from post-shipment support. An investment in robust handling repays itself in time and reputation, as client teams avoid complications from atmospheric moisture pick-up or accidental exposure during transfers.
Over multiple projects and partnerships, we have witnessed how 2-Amino-2'-Fluoro-5-Bromobenzophenone serves as a pivot point in a research pipeline. Medicinal chemists appreciate its versatility during scaffold hopping and fragment expansion. Process chemists leverage its reactivity for scale-up testing prior to commercial manufacture of final compounds. Custom synthesis firms adopt it for fast prototyping in exploratory SAR campaigns because of its clean conversion profile. This broad utility emerges not just from chemical structure, but from the real-world consistency we have achieved in managing quality at every batch scale. We continue to gather input from users targeting novel targets in oncology, infection, or central nervous system diseases, translating their feedback into tighter process controls and greater flexibility in order fulfillment.
Pharmaceutical companies, especially those progressing candidates to regulatory submission, have called for traceability and full documentation. We have created batch-level data packs, including COAs and analytical spectra, as part of standard operating procedure. We understand that minor impurities, if not tightly monitored, can jeopardize entire patent submissions or agency filings. Analytical chemists in our own labs and in partner organizations have evaluated this product for compliance with the latest guidelines, from elemental analysis to impurity profiling. These real efforts safeguard not just our product, but also our partners’ routes to commercial success. Our QA systems bring together raw data and in-process checks learned from repeated internal audits, cutting project risk before it ever affects a customer.
Producers farther down the supply chain, including CMO and CDMO partners, regularly send detailed reports on perceived gaps or process enhancements. One pattern stands out: documented benefits in overall throughput and reduction in unwanted side products compared with less functionalized benzophenone intermediates. This has led us to invest in pilot programs testing solvent systems that minimize residual contamination or analytics suites that speed up turnaround. We do not operate in a vacuum. Technical exchanges—factory tours, joint trouble-shooting calls, and round-table discussions with client chemists—have pushed us toward higher transparency and reproducibility. These two factors together set apart manufacturers focused on building long-term trust.
Despite its advantages, 2-Amino-2'-Fluoro-5-Bromobenzophenone has specific challenges that we do not hide from partners. Its increased functionality means limited solubility in certain non-polar solvents, thus impacting telomerizations or polymerizations based purely on dispersion. Some downstream conversions demand very dry handling, upping requirements for both storage and in-process protection from the elements. Not every reaction benefits from its dual electron-withdrawing and electron-donating effects; practitioners attuned to syntheses based on unfunctionalized benzophenones may need method development to unlock similar yields. As we work alongside teams investigating polymeric or materials applications, these parameters are flagged and discussed transparently. No intermediate solves every synthetic problem, but understanding these details in advance leads to more successful—and cost-efficient—project outcomes.
The evolution of our manufacturing line for this compound matches the fast-moving pace of medicinal and process chemistry today. We reinvest in pilot-scale testing, new purification techniques, and external collaboration as a matter of course. Our team regularly updates internal process maps as customer needs shift or new downstream applications arise; discoveries in reactivity or compatibility are built into the next production cycle. This has created a knowledge-sharing network with clients, feeding their results back into our upstream protocols. Our approach relies on seeing real syntheses, real project challenges, and not just relying on theory or standard references. The outcome: material that consistently does its job, arriving ready for the next stage of discovery.
Every gram of 2-Amino-2'-Fluoro-5-Bromobenzophenone reflects lessons learned in laboratories, close communication with customers, and the unending push for repeatable, reliable outcomes. The feedback loops between manufacturing staff, quality analysts, and front-line researchers have shown their importance with every successful scale-up and ongoing collaboration. As industries worldwide move toward more personalized, responsive chemistry, we remain committed to delivering materials that support, rather than constrain, innovation. By maintaining high standards not just in compound synthesis, but in every logbook entry, shipment, and client interaction, we see real science move forward—one reliable intermediate at a time.