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Methyl 3-(Cyclopropylamino)-2-(2,4-Dichloro-5-Fluorobenzoyl)Acrylate

    • Product Name Methyl 3-(Cyclopropylamino)-2-(2,4-Dichloro-5-Fluorobenzoyl)Acrylate
    • Alias MCDFBA
    • Einecs NA
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    451536

    Cas Number 1442362-90-2
    Molecular Formula C14H12Cl2FNO3
    Molecular Weight 348.16
    Iupac Name Methyl (E)-3-(cyclopropylamino)-2-(2,4-dichloro-5-fluorobenzoyl)acrylate
    Appearance White to off-white solid
    Solubility Soluble in organic solvents like DMSO and DMF
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Smiles COC(=O)C(=C(NC1CC1)C2=O)C2=C(Cl)C=CC(F)=C2Cl
    Inchi InChI=1S/C14H12Cl2FNO3/c1-22-14(20)11(18-7-6-8-18)13(19)10-4-9(15)2-3-12(10)17-5-16/h2-4,6,8H,5,7H2,1H3,(H,17,19)

    As an accredited Methyl 3-(Cyclopropylamino)-2-(2,4-Dichloro-5-Fluorobenzoyl)Acrylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass bottle containing 5 grams of Methyl 3-(Cyclopropylamino)-2-(2,4-Dichloro-5-Fluorobenzoyl)acrylate, labeled for laboratory use.
    Shipping Methyl 3-(Cyclopropylamino)-2-(2,4-Dichloro-5-Fluorobenzoyl)acrylate is shipped in tightly sealed, chemical-resistant containers under ambient conditions. Packaging complies with all relevant regulations for hazardous chemicals. Proper labeling and accompanying documentation ensure safe transportation. Handle with care; avoid exposure to heat, moisture, and direct sunlight. Suitable for laboratory use only.
    Storage Store **Methyl 3-(Cyclopropylamino)-2-(2,4-dichloro-5-fluorobenzoyl)acrylate** in a tightly sealed container, protected from light and moisture. Keep at 2–8°C in a well-ventilated, dedicated chemical storage area away from incompatible substances (strong acids, bases, and oxidizers). Ensure proper labeling and use secondary containment to prevent leaks. Follow all local safety regulations for storage of hazardous chemicals.
    Application of Methyl 3-(Cyclopropylamino)-2-(2,4-Dichloro-5-Fluorobenzoyl)Acrylate

    Applications of Methyl 3-(Cyclopropylamino)-2-(2,4-Dichloro-5-Fluorobenzoyl)Acrylate in Industrial Manufacturing

    As a specialized manufacturer, we supply Methyl 3-(Cyclopropylamino)-2-(2,4-Dichloro-5-Fluorobenzoyl)Acrylate to downstream partners operating in advanced pharmaceutical synthesis, agrochemical actives, specialty polymer additives, and industrial analytical chemistry. Each segment utilizes the material according to stringent formulation protocols, regulatory frameworks, and production line requirements. Below we detail key industry applications, providing compliance, usage, integration, and final product information tailored to actual market needs.

    1. Pharmaceutical Intermediate for Antineoplastic Compounds

    Pharmaceutical manufacturers incorporate this compound as a critical intermediate during the synthesis of selective kinase inhibitors targeting oncology therapeutics. The acrylate’s steric and electronic characteristics enable sequential coupling reactions, supporting API assembly for molecules under FDA-approved and EMA-regulated clinical studies. Control of input ratio and reaction temperature achieves consistent conversion necessary to meet regulatory release specifications.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) guidance for APIs
    • Certificate of Suitability (CEP) for supply into the EU

    Typical usage ratio

    • 0.3 to 0.7 molar equivalents per API batch; adjusted based on route selection and conversion efficiency

    Downstream process integration

    • Charged in the initial condensation step to introduce the cyclopropylamino moiety within multi-step organic synthesis
    • Subject to controlled temperature and solvent polarity ranges to minimize side product formation
    • Continually monitored via in-process HPLC/GC for identification of completion prior to next step

    Final product types

    • Targeted kinase inhibitor APIs (active pharmaceutical ingredients)
    • Experimental antitumor pharmaceutical agent libraries
    • Reference standard substances for regulated drug development

    2. Synthesis of Herbicidal Active Ingredients

    Agrochemical formulators use the compound as a structural precursor for the development of advanced selective herbicide actives, particularly those requiring chloro-fluorinated benzoyl motifs. It functions in coupling or cyclization stages under strictly managed conditions for field-ready formulations, supporting activity, persistence, and crop safety profile mandates. The process requires monitoring material purity and optimizing ratio for reaction completeness.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • FAO/WHO Specification and Evaluation of Agricultural Pesticides
    • ISO 9001:2015 Quality Management for Plant Protection Products
    • REACH (EC) No 1907/2006 registration for chemical safety in the EU

    Typical usage ratio

    • 5–15% of overall synthetic feedstock by weight; precisely metered after impurity screening

    Downstream process integration

    • Added during stagewise ring closure or amidation following initial phenyl core derivatization
    • Reaction monitored through LC-MS and controlled for residual solvent limitation
    • Subsequent purification in compliance with agrochemical residue regulations

    Final product types

    • Pre-emergence and post-emergence selective herbicide actives
    • Active ingredient powder for agrochemical formulation
    • Technical concentrate intermediates for herbicidal blends

    3. Functional Monomer in Advanced Polymer Additive Manufacturing

    Specialty polymer and plastics manufacturers utilize the compound in the design of high-performance copolymers where halogenated aromatic segments impart thermal resistance and unique surface characteristics. The acrylate group facilitates radical polymerization or copolymer chain extension, while the cyclopropyl ring stabilizes bulk matrix properties. Ratio and sequence affect polymer architecture, requiring precise dosing and reaction time control to meet end-use regulatory requirements.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems in Polymer Industry
    • REACH (EC) No 1907/2006 compliance for polymer substances
    • ASTM D256 (Polymer Impact Resistance Test Methods)
    • Food Contact Materials Regulation (where applicable, e.g., EU No 10/2011)

    Typical usage ratio

    • 0.5–5% by monomer weight, tuned based on desired glass transition temperature and specific polymer property targets

    Downstream process integration

    • Fed into pre-polymer reaction vessels with vinyl and acrylate monomers in batch or continuous mode
    • Dosing based on in-line rheology and molecular weight distribution analysis
    • Integrated prior to thermal or UV-initiated polymerization cycles

    Final product types

    • Specialty copolymers for electronics and automotive insulation
    • High-temperature-resistant engineering plastics
    • Functional coatings for industrial surface protection

    4. Reference Standard for Analytical Method Development

    Analytical chemistry laboratories use the compound as a reference standard to develop and validate quantification methods for in-process quality control and regulatory release testing. Precise purity and batch traceability ensure accurate calibration across chromatographic and spectroscopic platforms. Material handling, dilution, and storage protocols align with GLP and ISO guidelines, supporting routine analysis during pharmaceutical, agrochemical, or new molecule development workflows.

    Industry compliance standards

    • ISO/IEC 17025:2017 (General Requirements for Testing Laboratories)
    • Good Laboratory Practice (GLP) OECD Principles
    • USP General Chapter <1225> (Validation of Compendial Procedures)
    • FDA Analytical Procedures and Methods Validation Guidance

    Typical usage ratio

    • 1–50 mg per analytical batch, dependent on detection limits and matrix complexity in specific method protocol

    Downstream process integration

    • Diluted and prepared as calibration standard for HPLC, LC-MS, or GC validation
    • Applied in system suitability testing and process consistency checks during scale-up and commercial production
    • Utilized in forced degradation and impurity profiling studies

    Final product types

    • Certified reference solutions for external and internal calibration
    • Quality assurance documentation compliant with regulatory inspections
    • Validated analytical methods for release and stability studies
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    Certification & Compliance
    More Introduction

    Methyl 3-(Cyclopropylamino)-2-(2,4-Dichloro-5-Fluorobenzoyl)Acrylate: A Direct Look at Its Role and Value

    Insight From the Production Floor

    Years of running syntheses and monitoring reactions at scale have taught us a few things. Certain molecules bring a unique mix to the table, bridging the gap between technical challenge and market necessity. Methyl 3-(Cyclopropylamino)-2-(2,4-Dichloro-5-Fluorobenzoyl)acrylate represents one such specialty, designed with both precision and performance in mind. The compound’s backbone, featuring the cyclopropylamino group paired with a dichloro-fluorinated benzoyl ring, delivers more than just a talking point for a formula. From day one, the design pointed at improved reactivity and the ability to tune physical properties during process development. This isn’t a broad-brush ingredient—applications pull it specifically for what it brings.

    Comparing It to Everyday Acrylate Esters

    Across the industry, acrylate esters crop up all over the place. Most production teams at chemical manufacturers cut their teeth on workhorse chemicals like methyl acrylate, but these basics miss much of the fine-tuned behavior required for advanced synthesis. Additions of halogens and a cyclopropylamino function set this product apart. Typical methyl acrylate simply won’t deliver the steric and electronic effects required for selective functionalization, nor can it handle fine structural control in intermediate building blocks for pharmaceutical and crop science work. If you’ve ever tried to couple plain acrylates under demanding conditions, the limits become obvious—yield drops, selectivity suffers, and impurity profiles get messy. With our fluorinated, dichlorinated, and cyclopropylamino-substituted variant, downstream modifications stay manageable, isolations go cleaner, and final products reach tighter specs.

    Specifications That Matter

    In this trade, the difference between lab-bench dreams and warehouse realities comes down to how consistent and clean the material runs. This acrylate, with its particular substitution pattern, resists random side reactions under elevated temperatures or during exposure to a range of functional group conditions. Hydrogenation, cross-coupling, or other palladium-catalyzed steps that normally challenge less robust acrylates go off with fewer headaches. The methyl ester carries its expected pungency, yet with the added substitutions, storage proves stable under dry nitrogen and in amber packaging. Throughout every scale-up, batch-to-batch reproducibility holds—with only minimal drift in melting point, color, and impurity content.

    You might take the dichloro and fluorine touches as basic tweaks, but in practice, they safeguard the ring from unplanned over-reactions. Early batches showed a reduction in unwanted hydrolysis during workup, and anyone who’s been stuck cleaning up byproducts on large scale knows how much this saves down the line. The cyclopropylamino group, selected for its rigid geometry, actually limits backside attack—this pays off in both stability and tighter control of stereochemistry when working toward chiral intermediates. Lax purity or misjudged moisture push the material toward off-notes and degrade downstream handling; by applying a rigorous release testing protocol for these batches, we ensure process operators receive what they require without the need to rework or re-purify.

    Why This Molecule?

    No one selects a compound like this for bulk manufacture or commodity resin work. The market turns to this structure most often during late-stage intermediate production in pharmaceuticals, especially where downstream complexity and regulatory scrutiny leave no margin for sloppiness. It isn’t unusual to see R&D teams spend months trying broader chemical space, only to circle back to this precise combination for its balance of reactivity and protection. In our own experience, teams reporting from pilot-plant campaigns highlight that yields stabilize once this precursor enters the flow.

    Quality-by-design methods weren’t conceived just for feel-good paperwork. They grew out of the practical problems of lost batches and regulatory recalls. With our own investments in in-process controls, we shave off the guesswork. By tapping real-world feedback from process engineers and scale-up chemists, we have refined the product’s consistency—whether it comes in a 25-kilo drum or a pilot-lot bottle for a pharmaceutical program. This is not just a story about specs, but about how those specs help somewhere down the road, when teams work at pressure, searching for reliable conversion every time.

    Performance in Key Reactions

    Let’s talk through two common tasks: C–N bond formation and palladium-catalyzed cross-coupling. Standard acrylates give up early under these conditions; color darkens, product streams become heterogenous, and chromatography grows non-trivial. The electron-withdrawing character driven by the dichloro and fluoro partners supports smooth transition metal catalysis. As we’ve seen in our work, those catalysts tolerate lower loadings and run closer to theoretical conversion. When using this acrylate, column load diminishes, waste reduces, and crystallization emerges as a real isolation route rather than a pipe dream.

    The cyclopropylamino group, classically ignored in old-school analogues, plays its part in medicinal chemistry protocols. Customers in pharmaceutical R&D rely on this functionality to add nearly ideal non-linearity to molecular scaffolds—an indispensable property for kinase inhibitors and related targets. The rigidity isn’t just a textbook flourish; it allows the compound to hold its shape even over longer storage, reducing polymerization risk and lessening the formation of byproducts under ambient conditions.

    Safety and Environmental Handling—Manufacturer’s Perspective

    Every chemical with a benzoyl or acrylate tag brings hazard baggage. Here’s what experience tells us: stability cuts down on handle-time risk. With this particular compound, run-to-run operational safety tends to improve, due to predictable flammability and toxicity curves. Our containment and effluent controls are tailored to fracture the release of chlorinated and fluorinated off-gas, minimizing any direct impact during spills, leaks, or handling errors.

    Waste management teams appreciate the reduced volatility. The structure’s resilience to hydrolysis lessens the risk of unintentional breakdown in aqueous waste streams—a win for both regulatory trust and cost containment. Severity of clean-up drills stays moderate—unlike some less-stable acrylates, which require bulk neutralization and elaborate layered containment. Our industrial hygiene protocols revolve around specific, measured risks linked with halogenated compounds, ensuring all downstream users—ourselves included—maintain compliance and minimize exposure.

    Investing in Analytical Confidence

    Analytical reproducibility runs at the heart of the difference between a specialty and a me-too chemical. NMR, LC-MS, HPLC—all run against strict criteria before we release a batch. You can routinely catch commercial methyl acrylate on supply chains with a median impurity of over 2%, but with our inclusion of fluorine and dichloride functionalities, out-of-spec carries a unique fingerprint, making detection easier and auditing more honest. We don’t leave this to chance. Operators pull real-time samples, run mid-process checks, and confirm final release with both external and in-house labs. The result: lower risk for surprise decompositions, more trust during hand-off, and a guarantee that the chemistry your project requires will perform as designed—not just in idea, but in practice.

    The Human Element: Team Approach to Quality

    It’s easy to get lost talking numbers, but any chemical plant’s strength rests with the attention and habits of its staff. Over the years, our teams have rooted out final-release problems by advocating double checks, real-time communication, and fast escalation when something reads “off.” Real improvements sprang from scheduled operator feedback sessions—where frontline chemists flag even faint changes in color or odor. In the real world, minor changes signal much larger issues down the line. Rather than waiting for the lab to discover a purity drift or a shipment to boomerang back over an impurity problem, we address these issues upstream.

    On our shop floor, every run of this acrylate undergoes a double-check for both water and solvent content. A little extra drying or one last polish in the filtration train might add a step, but it guarantees the next chemist doesn’t discover surprises in their glassware or reactor.

    Speaking to Real-World Use Cases

    Customers and partners often ask what sets this acrylate apart in active development programs. Take a medicinal chemistry campaign: speed of iteration matters, but reliability counts double. No point putting interesting analogues on paper if they stall on the bench—or gum up analytical runs. The mix of electron-withdrawing and geometry-locking groups gives chemists freedom to optimize, while still spinning out analogues that avoid overreaction.

    In our hands, the compound has advanced more quickly through scale-up and tech transfer than other acrylates bearing less complex substituents. Projects under tight timeframes—especially late-stage intermediates—benefit the most. Our direct experience tells us that every skipped rework and every simplified clean-up translate into hours and dollars saved, not to mention a faster journey to regulatory success or commercial launch.

    Learning From Difficult Batches and Project Feedback

    Not every lot comes off the line perfect. A manufacturer who claims zero error never spent a night tracing residue or retesting a stubborn drum. Lessons from the rare off-batch matter: sometimes, trace halide salt or an incomplete solvent swap emerges during storage. In these moments, rapid communication with our QA team pivots the batch back on course. Over time, driven by these corrections, we fine-tune the last steps of crystallization and drying to chase out these subtle contaminants.

    Feedback cycles with our largest customers highlighted not just problems, but long-term gains. Reports of easier downstream conversions, less need for repurification, and cleaner NMR spectra spoke louder than routine QC reports. Using this feedback as our map, tweaks to process control—like tighter monitoring on reactor profiles and filtration speeds—measurably extended shelf life and as-delivered purity.

    Looking Down the Pipeline: Adaptability and Future Demand

    Working as a manufacturer at the crossroads of fine chemicals means living with change. Trends in medicinal chemistry steer new attention to halogen-rich and geometry-tuned acrylates; regulatory environments keep growing sharper, pushing us to align quality and documentation in new ways. Demand isn’t static—it moves with innovation, and compounds like this acrylate keep evolving to match it.

    Upcoming applications aren’t all mapped, but early signals show expansion beyond core pharmaceutical routes. Agrochemicals, specialty polymers, and materials science groups recognize the advantages of rigid, electron-deficient carbon backbones. As research teams refine their own methodologies, this compound opens the door for new field trials, not just for efficacy but for environmental profile improvements. The tools and controls we developed for today’s market guarantee a strong foundation for tomorrow’s discoveries.

    Direct Engagement: Cooperative Problem Solving

    Change comes easiest with open lines between manufacturer and user. Engineers, chemists, and project managers don’t just buy a drum; they expect support and transparency. Our open feedback channels, technical discussions before each large campaign, and post-delivery follow-ups address technical hurdles directly. Whether it’s adapting solvent packages for a unique reactor setup or providing accelerated stability data for a regulatory file, every plant-based conversation brings us closer to our shared goal: process simplicity and batch security.

    Take the case of an international partner adjusting process conditions for scale-up: instead of a flat “no” to deviations, our R&D team simulates the altered runtime, flags possible problems, and works up a pilot solution. This approach has turned one-off reactions into long-term partnerships and helped stave off production hiccups before they happen. The more we share practical findings—be it better workup methods or improved containment practices—the wider the benefit spreads across the network of users.

    The Practical Edge—From Our Personnel to Your Process

    Every year, new intermediates cross our desks—each one asking for something a little different in process, purity, or packing. The challenge with this acrylate hasn’t just been in making it, but in making it reliably, with every shipment matching the last. Our personnel sweat the details others overlook: small shifts in drying, adjustments to distillation timings, repacking to avoid micro-leaks during long export lags.

    Long-haul stability presents no minor concern, especially as more projects now draw from global supply. For temperature-sensitive campaigns, we tailor packaging and logistics to maintain potency and reduce racing-the-clock scenarios. Process-wise, our teams know the smells, the drift, and the warning signs of a lot going sideways—responsiveness on the plant floor, not just on paper, separates genuine manufacturers from armchair operators.

    Final Thoughts From the Manufacturing Perspective

    Methyl 3-(Cyclopropylamino)-2-(2,4-Dichloro-5-Fluorobenzoyl)acrylate isn’t for every project, but for those that need what it offers, the path from production to end-use matters. Each run refines our approach a little further—not out of a checklist mentality, but out of respect for the chemists and engineers who trust us to deliver material ready for their next breakthrough. Direct communication, careful process control, and a continuous learning mindset have shaped the product’s real-world value, proving that a strong link between manufacturer and user always pays off, no matter the complexity of the molecule itself.