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Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-Furoate

    • Product Name Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-Furoate
    • Alias AKOS024057905
    • 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

    842377

    Chemicalname Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-furoate
    Molecularformula C14H8ClF3O3
    Molecularweight 316.66 g/mol
    Casnumber 1802782-12-2
    Appearance White to off-white solid
    Purity Typically >98%
    Solubility Soluble in organic solvents such as DMSO and DMF
    Smiles CCOC(=O)C1=C(C(OC1)=O)C2=CC=C(C=C2)ClC(F)(F)F
    Inchi InChI=1S/C14H8ClF3O3/c1-2-21-13(20)10-8(7-22-14(10)19)11-3-5-12(15)6-4-11-14(16,17)18/h3-7H,2H2,1H3
    Storagetemperature Store at 2-8°C

    As an accredited Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-Furoate 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 10 grams of Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-Furoate, labeled with safety and chemical information.
    Shipping This chemical, Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-Furoate, is shipped in tightly sealed containers, protected from moisture, light, and extreme temperatures. The packaging complies with chemical safety regulations, ensuring secure transport. Proper labeling, including hazard information, is provided. Handle only by qualified personnel in accordance with MSDS and relevant shipping guidelines.
    Storage Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-furoate should be stored in a tightly sealed container, away from moisture, light, and incompatible substances such as strong acids or bases. Store in a cool, dry, and well-ventilated area, ideally in a flammable chemicals cabinet. Ensure appropriate labeling and keep away from heat sources or ignition. Follow all relevant chemical safety guidelines.
    Application of Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-Furoate

    Applications of Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-Furoate in Industrial Manufacturing

    As the original manufacturer of Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-Furoate, we supply this intermediate primarily to downstream chemical producers focused on high-value, regulated markets. The following sections outline its key roles in core application tracks, detailing compliance, formulation integration, processing steps, and resulting finished product types used by industrial end-users.

    1. Agrochemical Active Ingredient Synthesis

    This compound meets the strict synthetic needs of established pesticide producers as a late-stage intermediate in the production of select herbicides and fungicides. Manufacturers use it for specific carbon–carbon coupling and furan scaffold extension steps where high yield and traceability are vital. Its application occurs under controlled reaction conditions to meet local and export compliance, particularly for regulated crops and environments.

    Industry compliance standards

    • OECD Guidelines for Testing of Chemicals
    • REACH Registration (EC/1907/2006, European Union)
    • EPA TSCA Inventory (United States)
    • China Crop Protection Quality Standard (GB28150-2011)

    Typical usage ratio

    • 5–15% by weight of total reactant mass in the key coupling reaction, depending on the herbicide or fungicide structural design and targeted synthesis scale.

    Downstream process integration

    • Introduced after initial workup as a coupling partner in Suzuki, Heck, or Stille-type cross-coupling reactions, often as the precursor to pyridinyl or benzo-fused system formation in multi-step synthesis routines, before the final salt conversion and formulation phases.

    Final product types

    • Post-patent herbicide actives
    • Novel fungicide technical concentrates
    • Pre-mix and suspension concentrate agrochemical formulations
    • Regulatory-dossier-grade active ingredient batches for global registration

    2. Pharmaceutical API Intermediate

    Leading pharmaceutical manufacturers utilize this compound as a non-GMP intermediate for research-scale and pilot-scale synthesis of active pharmaceutical ingredients with complex heterocyclic architectures, especially in development of anti-inflammatory or CNS-disorder candidate molecules. The process requires careful validation of trace-level impurities and traceability to audit readiness, due to its structural motifs contributing to final API functionality.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP General Chapter <797>
    • EMA Guideline on the Chemistry of Active Substances (EMA/454576/2016)
    • 21 CFR Part 210/211 (FDA Quality System Regulation)

    Typical usage ratio

    • 2–7 molar equivalents, as dictated by the stoichiometry of the key cyclization or condensation stage in the API synthesis; adjustment follows process verification batch outcomes and impurity profile control needs.

    Downstream process integration

    • Loaded in the penultimate step of multistep organic syntheses, acting as the furan-containing linker or scaffold builder; this occurs before final crystallization and purification of the API under validated batch record environments.

    Final product types

    • Clinical-stage bulk API samples
    • Reference standard APIs for dosage form development
    • Regulatory submission batches for Phase I/II trials
    • Comparative impurity standards for method validation

    3. Specialty Fine Chemicals for Electronic Materials

    Manufacturers of functional materials and coatings for printed electronics adopt this compound as a building block in synthesizing high-performance furan-based oligomers, which serve as dielectric matrices and adhesion promoters within electronic substrates. These companies value tight compositional control for consistent dielectric properties and compatibility with amorphous fluorinated systems.

    Industry compliance standards

    • IEC 60194-2: Printed Boards Design Quality
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 9001:2015 Quality Management Systems
    • IPC-4101B: Specification for Base Materials for Rigid and Multilayer Boards

    Typical usage ratio

    • 8–25% by mass as incorporated into precursor batch blends; modified to optimize solubility and glass-transition targets in specialty polymer synthesis workflows.

    Downstream process integration

    • Added during oligomerization or prepolymer formulation, typically forming part of the backbone structure of synthons for liquid dielectric films or functional coating solutions; integration is monitored via NMR and GPC for molecular weight distribution

    Final product types

    • Photo-imageable dielectric coatings
    • High-frequency circuit board films
    • IC encapsulation materials
    • Adhesion promoters in multilayer PCB manufacturing

    4. Advanced Polymer Modification in Engineering Plastics

    Producers of high-performance engineering plastics introduce this compound specifically in the modification of fluoropolymer and furan-containing copolymer systems where it acts as a co-monomer to impart chlorine and fluorine functionalities. End users require consistent molecular uniformity for extrusion, molding, and high-thermal-stress processing, enabling production of specialty components for demanding automotive and aerospace applications.

    Industry compliance standards

    • UL 94: Standard for Safety of Flammability of Plastic Materials
    • REACH Substances of Very High Concern (SVHC) Compliance
    • ISO 1872-1: Plastics – Generic Identification and Marking
    • ASTM D638: Standard Test Method for Tensile Properties of Plastics

    Typical usage ratio

    • 3–10% by weight as reactive comonomer, based on target glass transition temperature and desired mechanical reinforcement; dosage is established via iterative melt-processability trials and thermal gravimetric analysis.

    Downstream process integration

    • Charged during bulk polymerization or reactive extrusion; integration is monitored for complete reaction and dispersion, with in-line FTIR analysis to confirm functional group incorporation before downstream compounding and pelletizing.

    Final product types

    • Flame-retardant engineering plastic pellets
    • Functional copolymer resins for automotive under-hood parts
    • Precision-molded aerospace brackets
    • High-durability furan-fluoro copolymer blends for specialized sectors

    5. Intermediate for Active Dyes and Pigments

    Downstream specialty dye and pigment manufacturers employ this compound in synthesizing advanced colorants, leveraging the structure’s halogen and trifluoromethyl substitution for improved lightfastness and solvent resistance. The process requires tightly controlled addition to minimize batch-to-batch tonal variation in colorant production for industrial coatings and digital printing sectors.

    Industry compliance standards

    • ETAD Code of Good Practice (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers)
    • DIN EN ISO 9001:2015 for Quality Management in Dye Manufacture
    • GHS Classification for Labeling and Transport
    • REACH Annex XVII (Substances Restricted in Dye Production)

    Typical usage ratio

    • 0.5–3% by weight as a coupling precursor in dye synthesis, with adjustment to meet chromaticity and purity targets in final pigment batches.

    Downstream process integration

    • Introduced as an aryl-furan structure in the condensation phase following initial azo or anthraquinone preparation, prior to finishing operations like filtration, salt formation, and organic solvent cleaning

    Final product types

    • High-performance industrial coatings colorants
    • Inkjet pigment dispersions for digital printing
    • Automotive-grade specialty dyes
    • UV-resistant architectural pigment pastes
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    Certification & Compliance
    More Introduction

    Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-Furoate: A Closer Look from the Manufacturer’s Bench

    Introduction

    From the start, Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-Furoate always stands out in our production lineup for its specialized role in advanced chemical synthesis. Working with this compound in our facility reveals both its chemical character and its practical impact. Over the years, direct feedback from formulation chemists and our own hands-on processing guide our understanding of what sets this material apart.

    Model and Specifications

    We prepare Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-Furoate according to strict internal benchmarks because its molecular complexity demands attention to detail during every stage of manufacture. Our production model emphasizes reproducibility and purity, targeting a product that consistently delivers a purity level of above 98%. Every batch leaves the reactor after stringent analytical controls—NMR, HPLC, GC-MS—all traceable in our records. Any unexpected impurity triggers a process review before the material ever reaches a drum or bottle. These measures grew out of years spent investigating reaction efficiency and solvent interactions, since anything short of the best undermines user confidence and performance down the line.

    With its molecular formula C14H8ClF3O3, Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-Furoate offers a structural topography that responds predictably under both standard and creative synthetic conditions. The trifluoromethyl and chlorophenyl groups anchor its stability, letting chemists pursue reactions that challenge less robust compounds. We’ve studied its granular form and how it handles thermal stress, learning through trial and error the right storage and shipping parameters. Tightly sealed packaging guards against hydrolysis, and each unit follows a chain of custody documented by our internal QC team. I’ve watched our warehouse staff inspect every container for integrity, recognizing that a single compromised drum disrupts more than just a workday.

    Why Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-Furoate Matters

    Feedback from the pharmaceutical labs and custom synthesis groups showed us the real value of this molecule. In the early days, questions centered on scale-up reliability and solvent compatibility. Process engineers pointed out that materials with similar structures—furoates, for instance—frequently stumble during crystallization or form unwanted by-products. We focused on improving step yields and reducing process time, always comparing our protocol side-by-side with competing chemistries. The result: Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-Furoate quickly found favor among researchers looking to assemble complex heterocycles or explore new pathways in medicinal chemistry, especially where reactivity can shift over narrow temperature windows.

    It’s one thing to supply a bottle; it’s another to account for the headaches chemists face if a reaction stalls or contaminates a catalyst. We built our process around reproducibility, not just theoretical numbers. If solvent residues or batch-to-batch variations sneak past the line, trouble follows. The attention given to solvent choice, drying cycles, and trace metal content all comes from real mishaps in our own pilot plant. Each parameter lesson, hard-won after troubleshooting runs that didn’t meet downstream requirements, polished our methods.

    Applications and Usage Insights

    Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-Furoate supports a niche but growing set of applications, with the clearest demand from pharmaceutical development. Teams working on next-generation APIs reach for it to construct intermediates where electron-rich and electron-poor groups need to harmonize within the core structure. Organic chemists use its distinct electron arrangement and steric profile to drive reactions efficiently. I’ve seen firsthand how its reactivity suits Suzuki-Miyaura couplings, furan-based annulations, and selective acylation sequences. The feedback from innovation labs often focuses on minimized side product formation, cost-per-kilogram at pilot and commercial scales, and reproducibility under pressure—not the kind of points that show up on sales brochures, but the practical stuff engineers and bench chemists live by.

    The life of a molecule that passes through our reactors extends far past our loading bays. In agricultural synthesis, several teams confirmed its utility in designing candidates for crop protection, tying efficacy to the unique electron-withdrawing nature of the trifluoromethyl group and the presence of a 4-chlorophenyl ring within the furoate scaffold. These design elements open up options for novel bioactivities, which basic furoate esters cannot offer. Researchers exploring new herbicide or antifungal scaffolds often report that the compound’s sterics and stability allow for cleaner transformations compared to non-halogenated or non-fluorinated counterparts.

    Veterans of the flavor and fragrance industry dabble in this structure—not often, but for certain high-impact intermediates. The same features that guide pharmaceutical and crop science chemistry help form notes and building blocks that resist degradation, even under challenging processing conditions. The combination of durability and tunable reactivity generates attention in projects where predictable transformation is everything.

    Direct Comparison with Related Compounds

    Among compounds sharing either the furoate backbone or the distinctive 4-chlorophenyl motif, the addition of a trifluoromethyl group always makes a difference in both chemical resilience and reactivity. People sometimes ask why not use a simple ethyl furoate or substitute with a non-fluorinated variant. After testing and tracking the performance, the answer lies in the way reactivity profiles shift and how products withstand heat, moisture, or competing reactants. For custom syntheses targeting high-complexity APIs or robust crop science molecules, material with less robust side groups tends to falter during purification or late-stage functionalization.

    Our research group ran side-by-side reactions with non-chlorinated analogs. The 4-chlorophenyl group steadies the molecule during halogen exchange and palladium-catalyzed steps. Control experiments with methyl or propyl esters in place of ethyl usually produced inferior yields, further complicated by unwanted hydrolysis. That finding guided our choice to emphasize both the ethyl and halogenated motifs in our standard offering. Where project timelines are tight, and every by-product threatens a campaign, this difference pays off in fewer delays.

    There’s another dimension: environmental stewardship and regulatory compliance. Substituting or altering these motifs pulls the molecule into new regulatory categories, impacting both safety and disposal requirements. Years of feedback confirmed the market’s preference for established compounds that bring both high reactivity and less regulatory liability than some newly introduced scaffolds. By manufacturing Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-Furoate consistently, we help customers stay within accepted regulatory frameworks while still driving innovation in synthesis.

    Challenges in Production and Solutions

    Producing complex fluorinated aromatics with both high yield and purity never comes easy. Our staff watched yields erode in early campaigns until we overhauled our distillation apparatus and upgraded in-line monitoring. Batch failures drove home the need for aggressive reviews of every process parameter: from reaction temperature to solvent conditioning, even down to the quality of our glassware coatings. A single trace metal or an undercooked dehydration step spelled knock-on effects through every downstream process. These production headaches forced us to chart hundreds of runs before we could trust a process recipe. Any slip meant lost raw materials, downtime, and urgent calls to R&D.

    Our plant engineers now insist on regular equipment validation schedules. Automated sampling hooked directly to the laboratory means we identify variances before they can snowball. We built flexibility into our process recipes so chemists can adapt for minor feedstock differences without resorting to stopgap fixes. Investments in enzyme-compatible solvents and greener extraction approaches allowed us to reduce both waste and energy use across multiple runs—lessons learned during both successful and failed pilot batches. Each improvement grew out of identifying exactly where older analogs fell short, then tasking our team to deliver incremental gains each quarter. These small, steady steps now define how the process works, rather than dramatic step changes that raise costs and risk.

    From our end, every kilogram packed reflects hours spent tracking down sources of impurity charge. The result: downstream customers notice fewer batch rejects, and technicians see more predictive processing times. Regulatory audits, which once induced anxiety, now prove manageable thanks to verifiable, on-record controls at every hand-off.

    Supporting Research and Continuous Improvement

    Beyond just manufacturing, we keep in regular contact with researchers pushing the frontiers of chemical and pharmaceutical synthesis. Collaborative trials often unearth new uses, or unexpected bottlenecks triggered by scale-up. Our technical support teams routinely gather process feedback, logging everything from product solubility in mixed binary solvents to batch filtration challenges. If a lab reports an anomaly—a cloudiness in a solution, an unaccounted-for loss on drying—our staff dig into the sampling procedure and replicate the challenge. Every customer issue becomes a learning tool for further refining our process.

    Feedback also guides our compound’s evolution. One major advantage stems from direct observation of how different user groups work with the product. For instance, researchers tackling air-sensitive reactions can now request specialized packaging flushed with inert gas. Shipment schedules shift to accommodate time-critical lots needed for pharmaceutical validation. We partner with local and international shipping firms able to maintain strict temperature and humidity control, investments that came only after real-world mishaps on the delivery side. Each adjustment reflects trust built up with customers who rely on our material for breaking new ground.

    Adapting to Evolving Market Needs

    Markets change—new synthetic methodologies, evolving regulatory requirements, and the yearly rotation of research priorities. From where we stand at the manufacturing line, the focus stays on providing reliable, traceable, and consistent product no matter these outside shifts. By visiting industry consortia, attending project kickoffs at major R&D hubs, and hosting technical exchanges with academic partners, we ensure our staff stays ahead of both chemical innovation and regulatory trends.

    Several years ago, regulatory bodies tightened oversight on handling and storage of fluorinated compounds. We responded by retrofitting our storage tanks, revising SOPs, and investing in real-time monitoring. These shifts did not happen in isolation—customer engagement shaped every step, with requests for cleaner documentation, easier batch recalls, and transparent residual solvent testing shifting how logistics work at the shop floor level. The lessons from handling Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-Furoate shaped how we now approach improvements for any complex fluorinated or halogenated materials.

    Environmental Responsibility and User Protection

    Manufacture of fluorinated and halogenated organics draws environmental scrutiny. We face the same questions as our customers regarding safe disposal, airborne emissions, and long-term ecological persistence. Our plant uses closed-loop solvent recovery combined with regular waste audits to keep emissions below the strictest benchmarks. Investments in on-site water and air purification grew out of both regulatory requirements and respect for the local community. These upgrades carry real costs, but experience proved that cutting corners ends up expensive in both fines and lost business.

    Waste minimization efforts spring from watching early runs run afoul of local disposal guidelines. By switching to less hazardous process aids and sending regular samples for third-party effluent testing, we cut both risk and cost. These practices form part of the stewardship that lets our customers trust our material for both industrial and research purposes, confident that the chain of responsibility starts at the source.

    User protection gets built in, too. Training begins long before operators see a new raw material or process—each technician takes part in live run-throughs covering handling, potential hazards, and first response to exposure. Direct experience—reviewing how spills or mishandling events unfolded in our own facility—shapes the depth and regularity of training. Labelling systems trace every can, carton, or drum through production, so nothing leaves our plant without a trail. These steps reflect a hard-won belief that end-user success starts with robust processes at the point of manufacture.

    The Manufacturer’s Perspective

    After years on the plant floor and in direct line management, I can say that Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-Furoate exemplifies what thoughtful, informed manufacture means for research-driven industries. We live the stresses and discoveries of each campaign, each run a window into where material quality, process know-how, and customer partnership intersect. Our confidence in this compound does not come from a single set of lab data or a marketing sheet, but from a history of solving practical problems—from drum leaks to tricky purifications and challenging scale-ups.

    Customers notice how quickly they can slot our batches into their existing recipes. Those relationships grew over countless phone calls, shared experiment logs, and fielding urgent troubleshooting requests at inconvenient hours. Every improvement cycle in our warehouse or loading dock reflects the needs of end-users who can’t afford downtime or risk batch failures. Our teams now know how seemingly minor tweaks—dryer cycle length, solvent ratio, filter grade—carry through to the success of entire synthesis sequences. Each production run carries layers of experience, feedback, and learning that extend far beyond the simple transfer of molecules from one vessel to another.

    Looking Forward

    As demand for unique furoate derivatives increases, we believe staying attentive to both technical detail and user feedback will remain the backbone of quality manufacturing. New technologies and regulatory shifts will keep challenging the ways Ethyl 5-(4-Chlorophenyl)-2-(Trifluoromethyl)-3-Furoate fits today’s and tomorrow’s needs. Our approach remains focused on honest communication, clear documentation, and a willingness to adapt—qualities shaped by the practical realities of chemical production. Every bottle, drum, or batch of this compound tells a bigger story—one where quality, safety, and partnership live at the source.