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2-Bromo-2-(2-Fluorophenyl)-1-Cyclopropylethanone

    • Product Name 2-Bromo-2-(2-Fluorophenyl)-1-Cyclopropylethanone
    • Alias BRD-K63353552
    • Einecs 817-924-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    989067

    Product Name 2-Bromo-2-(2-Fluorophenyl)-1-Cyclopropylethanone
    Molecular Formula C11H10BrFO
    Molecular Weight 257.1 g/mol
    Cas Number 1421373-95-0
    Appearance White to off-white solid
    Purity Typically ≥98%
    Smiles C1CC1C(=O)C(Br)c2ccccc2F
    Inchikey JUTKYNFNPGGHQS-UHFFFAOYSA-N

    As an accredited 2-Bromo-2-(2-Fluorophenyl)-1-Cyclopropylethanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Supplied in a 5-gram amber glass bottle with a tamper-evident cap; labeled with chemical name, CAS number, and hazard warnings.
    Shipping 2-Bromo-2-(2-Fluorophenyl)-1-Cyclopropylethanone is shipped in tightly sealed containers, protected from light and moisture. Handling follows all applicable chemical safety and transport regulations. Packages are clearly labeled with hazardous material warnings and include appropriate documentation. Temperature control may be required, depending on specific stability requirements of the compound during transit.
    Storage Store 2-Bromo-2-(2-Fluorophenyl)-1-cyclopropylethanone in a tightly sealed container, in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Use appropriate personal protective equipment when handling, and avoid prolonged exposure. Follow all local regulations for storage and disposal of chemical substances.
    Application of 2-Bromo-2-(2-Fluorophenyl)-1-Cyclopropylethanone

    Applications of 2-Bromo-2-(2-Fluorophenyl)-1-Cyclopropylethanone in Industrial Manufacturing

    Our production-grade 2-Bromo-2-(2-Fluorophenyl)-1-Cyclopropylethanone serves as a core intermediate deployed by leading innovators in specialty chemicals, pharmaceuticals, and agrochemical active ingredient synthesis. The following downstream application scenarios reflect established industrial practice, based on our long-term supply, client feedback, and formulation guidance aligned with global regulatory demands.

    1. Advanced Pharmaceutical Intermediate for CNS Drug Synthesis

    Downstream manufacturers rely on this compound during the multi-step synthesis of potent central nervous system modulators, especially within research and commercial-scale workflows for anticonvulsant and neuroprotective drug candidates. Its unique structure enables selective introduction of brominated and fluorinated motifs into ketone-functionalized scaffolds as early-stage intermediates, supporting regulatory-compliant process development in batch and flow regimes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • EU GMP Part II APIs compliance (EudraLex Vol. 4)
    • 21 CFR Part 210/211 US cGMP
    • Relevant chapters of the Chinese Pharmacopoeia regarding intermediate manufacturing

    Typical usage ratio

    • Employed from 0.4 to 0.7 molar equivalents per synthetic route step; integration adjusted to protect group strategy and desired yield targets.

    Downstream process integration

    • Charged during Step 3 or 4 of convergent alkylation or halogenation reaction blocks; used prior to ring closure or heterocycle formation to preserve aryl halide integrity.

    Final product types

    • Active pharmaceutical ingredients (APIs) for antiepileptic drugs
    • Specialty neuropharmaceutical intermediates
    • Preclinical CNS research compounds
    • Key step intermediates for regulatory submission

    2. Agrochemical Active Core for Herbicide & Fungicide R&D

    Process development labs and industrial agrochemical producers employ this raw material as a coupling partner for the preparation of brominated and fluorinated aryl keto-based herbicide and fungicide cores. The high purity profile supports registration dossiers and consistent field performance trials.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice
    • ISO 9001:2015 Quality Management (chemical synthesis)
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) requirements for intermediates
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) guidelines for formulation inputs

    Typical usage ratio

    • Incorporated at 5% to 10% w/w in batch processes; adjusted based on the degree of aryl substitution required for target active scaffold development.

    Downstream process integration

    • Introduced post-nucleophilic aromatic substitution; participates in dehydrohalogenation and further cyclization, streamlining active core assembly for registration-standard pesticides.

    Final product types

    • Pre-commercial herbicide intermediates for cereal crops
    • Registration-stage fungicide lead compounds
    • Pilot-scale aryl keto-based pesticide actives
    • Sample-scale toxicology test materials

    3. Fine Chemical Precursor for Fluorinated Specialty Materials

    Producers of high-value, functionalized fluorinated compounds use this material as an essential building block during the elaboration of custom ketone architectures for performance materials and analytical standards. Its cyclopropyl and aryl substitution pattern uniquely enables access to rigid, fluorinated molecular frameworks.

    Industry compliance standards

    • ISO 14001 Environmental Management for chemical manufacturing
    • GHS (Globally Harmonized System) chemical handling protocols
    • REACH-compliant substance tracking and usage reporting
    • Japanese Chemical Substances Control Law (CSCL) as applicable for imports

    Typical usage ratio

    • Typically loaded from 2% to 6% w/w, depending on target product molecular weight and fluorine content specifications.

    Downstream process integration

    • Dosed at the initial build-up stage; further functionalized via Grignard addition or cross-coupling to yield semifinished specialty monomers or analytical reference standards.

    Final product types

    • High-performance fluorinated monomers
    • Analytical reference chemicals for spectroscopy
    • Calibration solutions for GC and LC applications
    • Custom fine chemical intermediates

    4. Intermediate for API Grade Brominated Aromatic Ketones

    Proprietary routes toward advanced pharmaceutical building blocks, especially where a combination of bromine and fluorine functionalities is critical, utilize this material in multi-step synthesis. Its consistent quality reduces batch-to-batch variability in complex pharmaceutical manufacturing lines.

    Industry compliance standards

    • US Pharmacopeia (USP) monograph requirements for pharmaceutical intermediates
    • EDQM Certificates of Suitability (CEP) reference standard adherence
    • ICH Q11 Development and Manufacture of Drug Substances
    • Good Distribution Practice (GDP) for APIs

    Typical usage ratio

    • Used at 0.3 to 0.5 molar equivalents per step, with ratio changes determined by the scale of batch and process validation requirements.

    Downstream process integration

    • Fed into the bromination or fluorination step just prior to condensation, often forming the reactive keto-aryl intermediate for subsequent heterocycle formation under GMP conditions.

    Final product types

    • API-grade aryl ketone intermediates
    • Brominated aromatics for clinical development
    • Building blocks for advanced oncology and CNS APIs
    • Regulatory filing intermediates

    5. Raw Material in Custom-Designed Research Chemicals

    Synthetic organic chemistry firms and research laboratories incorporate this compound as an advanced precursor in target-oriented synthesis where both fluorine and cyclopropyl moieties impart unique biological or physical properties for novel molecule creation, typically under strictly documented research protocols.

    Industry compliance standards

    • ISO 9001:2015 for laboratory synthesis
    • Material transfer agreement (MTA) protocols for restricted chemical use
    • National regulatory requirements: US EPA TSCA, EU REACH Article 3(15) research exemptions
    • Local environmental health and safety (EHS) requirements for laboratory chemicals

    Typical usage ratio

    • Ranges from 1% to 15% by reaction mass depending on the custom synthetic route and targeted molecular library diversity.

    Downstream process integration

    • Added early in in-situ reactions, often preceding scaffold elaboration or diversification steps, particularly in combinatorial synthesis environments.

    Final product types

    • Small molecule screening libraries
    • Novel chemical entities (NCEs) for patent filing
    • Structure-activity relationship (SAR) study compounds
    • Specialty research reagents
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    Certification & Compliance
    More Introduction

    2-Bromo-2-(2-Fluorophenyl)-1-Cyclopropylethanone: A Reliable Intermediate for Precision Chemistry

    Modern Approaches to Advanced Building Blocks

    Over the years, we have watched the demand for specialty pharmaceutical intermediates shift from basic aryl halides and alkyl bromides to highly engineered, functionally dense molecules. 2-Bromo-2-(2-Fluorophenyl)-1-Cyclopropylethanone holds a firm position in this space. In our production lines, achieving this compound with strong batch consistency helps downstream research groups advance their syntheses, especially in fields that explore new heterocyclic cores or modified kinase inhibitors.

    Clients approach us with challenging targets that benefit from robust phenyl ring modifications. We see the fluorine atom on the aromatic ring not just as a simple addition, but as a precision adjustment that can shift physiochemical behavior, improve metabolic stability, and carve out new pharmacokinetic profiles. Our lines focus tightly on the relationship between substitution pattern and reactivity, which comes into play heavily for this specific ketone building block.

    Sourcing from deeper inside the chemistry means we work closely with process engineers and chemists who expect more than an off-the-shelf option. Feedback from our collaborative work with pharmaceutical scientists highlights how a single misplaced impurity or a slight shift in crystallinity can derail sensitive downstream reactions or introduce regulatory headaches. Maintaining a tight rein on spectral purity and minimizing side-reactions defines how we approach every production batch.

    The Importance of Stereochemistry and Substituent Effects

    Early in our process development, we tuned in to how cyclopropyl structural elements add rigidity and confer unusual resistance to metabolic transformation. This small alkyl ring pushes adjacent groups into conformations that don’t occur with simple ethyl or isopropyl analogues. In 2-Bromo-2-(2-Fluorophenyl)-1-Cyclopropylethanone, the interaction of the cyclopropyl and the bromo-ketone center creates a unique entry point for nucleophilic substitution or coupling.

    Many chemists compare this structure to more conventional chloro or bromophenyl ketones. What we notice during synthesis is that the fluorine atom plays a subtle but important role. Introducing a fluorine atom at the ortho position (beside the bromo-substituted carbon) both slows and tunes the reactivity—the electron-withdrawing effect tightens up the aromatic ring’s behavior, impacting yields, selectivity, and even shelf-life. Only through frequent stability studies and repeated batch tests do we see the cumulative impact on larger scale projects.

    We made several modifications to our reactors and purification setups to meet this challenge. The presence of a cyclopropyl group means typical distillation and crystallization methods may fail to cleanly separate side products. Instead, we rely on a series of adjustable temperature profiles and slow, staged filtration to reach the levels of purity that innovative medicinal chemists require. Our in-house analytics help us spot subtle differences in melting point or NMR signature that can flag downstream issues before they arise.

    Practical Applications in Today’s Research

    Before any new synthetic pathway moves forward, our QA teams hold discussions with customers on the tiniest aspects of the molecule's role: Is the bromine intended for direct palladium coupling, or as a handle for heteroatom introduction? Is the cyclopropyl tailored for shape-selectivity in enzyme binding? In the workflows we service, 2-Bromo-2-(2-Fluorophenyl)-1-Cyclopropylethanone acts not only as a reaction partner, but often as a control compound in biological screens or as a standard for method development.

    Over the past year, collaborators in agrochemical research shared that the rigid ethyl group (from traditional analogues) allows too much movement, generating off-target activity. Cyclopropyl, on the other hand, arrests that motion, letting them design more selective bioactive agents. In contract manufacturing, we've often been called to troubleshoot synthesis slowdowns stemming from impure starting ketones—a recurring story in high-throughput medicinal chemistry, where tens or hundreds of analogues get run through in parallel.

    Comparative Insights: Going Beyond Commodity Ketones

    We have handled a diverse set of substituted aryl ketones over two decades. Many customers initially work with 2-bromo-2-phenyl-1-cyclopropylethanone or its para-fluoro variant. The ortho-fluorine modification introduces just enough electronic change to open new options for cross-coupling and nucleophilic attack. Compared to unfluorinated versions, we routinely measure enhanced resistance to hydrolysis and improved storability (under cold, dry conditions).

    Researchers who move from para- to ortho-fluoro analogues often observe that reaction profiles shift in reproducible but initially unexpected ways. Our production team saw yield improvements in Suzuki couplings with the ortho-fluoro compound, along with easier purification due to less byproduct formation. These details don’t show up in generic catalogs—they stem from lots of batches, lots of hands-on, and endless troubleshooting.

    We place high value on transparency with our partners. If a batch varies in color, odor, or crystalline habit, our analytical chemists don’t assume the difference is trivial. They trace back through every step—solvent grades, time at temperature, even differences in raw material suppliers—and share those data with our clients. This gives researchers solid footing when optimizing their target molecule syntheses.

    Tuning the Supply for Scale and Speed

    We never underestimate the unpredictability of moving a promising reaction from milligram vials to multi-kilogram production. Many find, to their frustration, that batch-to-batch variability in specialty reagents puts their timelines and budgets at risk. Years ago, after receiving reports of crystallization failures from one of our overseas clients, we revisited our filtration and storage procedures. Our facility shifted ambient storage to temperature-controlled, progressive cooling, based on observed changes in melting range.

    Experience trained us to coordinate with scale-up teams on every variable: solvent profiles, order of addition, and even stirring speed. The ketone’s bromo functionality can lead to off-pathway products via elimination or rearrangement, especially if too much heat gets into the system. By carefully collecting feedback from every synthesis step and integrating feedback from partners across the pharma, agchem, and R&D spectrum, we have refined our process to reduce unreacted bromo precursors and boost isolated product yield.

    This dialogue lets us give our partners a realistic picture: not every lot will behave identically in novel catalysis screens, but understanding the likely ranges saves weeks of re-optimization. The vast majority of our large-scale deliveries arrive within purity specs, and we’re candid about any observed deviations, offering direct batch samples for reactivity pretesting. That openness forms the backbone of our customer relationships, especially with fixed project deadlines in high-stakes development programs.

    Environmental Responsibility and Process Safety

    Brominated and fluorinated intermediates come with clear regulatory and environmental challenges. During the early years, standard operation meant accepting routine bromine emissions and non-recoverable fluorinated waste. We pivoted strongly after local authorities highlighted the cumulative impacts of such streams on wastewater and air quality metrics. Our investment in advanced capture and neutralization reflects not just compliance, but protection for our team and community.

    Today, all of our reaction off-gas passes through dual scrubbing columns, and our spent reaction mass gets collected for downstream incineration at certified facilities. Our internal audits track both product throughput and waste ratios, allowing us to dial down hazardous discharges per kilogram of product. We also partner with responsible solvent recyclers, since the main solvents in 2-Bromo-2-(2-Fluorophenyl)-1-Cyclopropylethanone synthesis include halogenated hydrocarbons and ketones, each with unique classification.

    Our chemists regularly meet with safety teams to examine each stage for possible leaks, overpressure risks, or exposure incidents. Every move to greener reagents gets considered, though the performance requirements for bromination and cyclopropylation remain strict. As a manufacturer, our commitment is not just technical delivery—it's stewardship of process risk and environmental footprint, keeping both regulators and neighbors in the loop.

    Adapting to the Fast-Moving Regulatory Landscape

    Regulatory frameworks governing specialty organofluorine and organobromide intermediates evolve constantly. International agencies, including REACH and TSCA, update hazard and transport codes as new toxicological data emerge. Some buyers hit snags with imports or find themselves navigating unknown documentation hurdles, which can impact project milestones. Being a direct manufacturer, not a middleman, puts us in a strong position to provide full pedigree—from raw material intake through to final lot testing.

    Over the last decade, our regulatory experts worked alongside compliance staff from end-user companies. Together, we interpreted new substance restrictions, tailored storage and shipping protocols, and built robust traceability for every kilo produced. We keep all test data (NMR, GC-MS, HPLC, and melting range) tied to individual batches, not just generic specs, giving both auditors and research staff a high degree of confidence. In a market increasingly crowded by short-term traders, our track record for meeting regulatory scrutiny gives our clients peace of mind.

    Challenges in Demand Forecasting and Lead Times

    Planning for production of advanced intermediates, especially those with specialized substitution, brings seasonal ebbs and peaks. Lead times fluctuate when pharmaceutical or agrochemical partners hit fast-tracks or switch projects. Our facility manages both campaign-based and just-in-time scheduling, relying on up-to-date demand signals from recurring partners. While some producers cut corners to chase spikes, our long-term relationships allow us to forecast more realistically.

    The most challenging situations arise when scale-up requirements climb suddenly—such as a project entering a clinical phase. For 2-Bromo-2-(2-Fluorophenyl)-1-Cyclopropylethanone, we maintain strategic in-process inventory, but remain nimble enough to adjust for custom solvent or packaging requests. Our plant has invested in broader reactor volumes, and we continually cross-train our technical team between cyclopropylation and halogenation lines. This elasticity allows us to meet tight deadlines without trading away quality or compliance.

    The Importance of Open Communication

    Direct communication has repeatedly helped us catch issues early and tune our schedules. Once, an end-user flagged unexpected color changes on arrival for a multi-kilo order. Instead of delaying projects with bureaucratic investigation, we connected main bench chemists from both labs. Together we tested small samples, swapped notes, and isolated minor variations traced to an earlier batch of bromine—not a plant-wide issue, but a single supplier anomaly. That exchange avoided a production halt, demonstrating what shared technical language and transparency accomplish in time-sensitive manufacturing.

    We maintain that producing 2-Bromo-2-(2-Fluorophenyl)-1-Cyclopropylethanone is a partnership, not just a transaction. We invite our clients to audit facilities, review batch histories, and discuss any process challenge that might affect outcome. By working shoulder-to-shoulder with technical teams on both sides, we continually raise the bar on reliability and responsiveness. We make ourselves available for reformulation projects and rapid scale-ups, staying committed for the entire research and development cycle.

    Product Differentiation: What Experience Teaches

    Extensive field experience sets apart our material from lower-grade competition. Some companies, primarily brokers or resellers, pass along off-spec or out-of-date lots, hoping for a quick sale to an undiscriminating buyer. Our in-house approach means direct control at every phase—no substitutions, no unexpected packaging swaps, no generic paperwork. Each delivery comes straight from our regulated lines, with the assurance that storage, handling, and analytical oversight remain in our hands from start to finish.

    We do not cut corners on solvent quality or overlook temperature excursions that might degrade reactivity. Our teams run full-spectrum testing, not just basic aryl or ketone ID checks. By monitoring secondary peaks in NMR and checking for minor shifts in melting point, we keep batches aligned for even the most exacting research requirements. This focus on technical excellence, backed up by traceable production records, provides a consistent base for users innovating at the frontiers of modern chemistry.

    Supporting Innovation with Practical Know-How

    Innovation thrives on a foundation of reliable supply. Our decades in chemical manufacturing help us anticipate, and forestall, many of the stumbling points that hit research teams venturing into new territory. For many, 2-Bromo-2-(2-Fluorophenyl)-1-Cyclopropylethanone is not just another intermediate, but an enabling molecule in their project. Our mission is to provide the seamless service, flexible response, and high-grade material needed for complex, scalable syntheses.

    We routinely update our finished product guidelines, integrating feedback from the laboratory bench and plant floor alike. Some clients want new custom packaging to match automated solid dosing; others require variant particle sizes. Our blending and handling teams adjust to ensure each order fits directly into the customer’s workflow, saving time and reducing costly clean-out between products. That degree of adaptation sets us apart among specialty chemical producers.

    Our long-term partners put their trust in consistent delivery and forthright communication, knowing that small differences in starting materials can yield major breakthroughs—or major obstacles. We respect that trust by keeping clients in the loop at every decision point, and by investing in upfront process improvements, rather than waiting for problems to emerge downstream.

    Conclusion: A Reliable Partner for Progress

    Success in modern organic chemistry rides on the backbone of dependable, high-quality building blocks. With 2-Bromo-2-(2-Fluorophenyl)-1-Cyclopropylethanone, we deliver not only a molecule but the benefit of our full experience as a manufacturer. Each batch reflects years of accumulated know-how, honest communication, and a commitment to responsible production. Users can move forward with confidence, backed by a supply partner who understands the chemistry, respects the regulatory environment, and works every day to support new discoveries.