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2-Benzofurancarboxylic Acid Ethyl Ester

    • Product Name 2-Benzofurancarboxylic Acid Ethyl Ester
    • Alias Ethyl 2-benzofurancarboxylate
    • Einecs 218-702-0
    • 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

    411468

    Chemical Name 2-Benzofurancarboxylic Acid Ethyl Ester
    Cas Number 57840-18-5
    Molecular Formula C11H10O3
    Molecular Weight 190.20 g/mol
    Appearance Colorless to pale yellow liquid
    Density 1.192 g/cm3
    Boiling Point 318.8 °C at 760 mmHg
    Refractive Index 1.535
    Purity Typically ≥98%
    Smiles CCOC(=O)C1=CC2=CC=CC=C2O1
    Inchi InChI=1S/C11H10O3/c1-2-14-11(12)9-7-8-5-3-4-6-10(8)13-9/h3-7H,2H2,1H3
    Solubility Slightly soluble in water; soluble in organic solvents
    Storage Condition Store at room temperature, keep container tightly closed
    Synonyms Ethyl 2-benzofurancarboxylate

    As an accredited 2-Benzofurancarboxylic Acid Ethyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Glass bottle with secure cap, 25g label, chemical name, purity, hazard symbols, batch number, and handling instructions printed clearly.
    Shipping 2-Benzofurancarboxylic Acid Ethyl Ester is shipped in tightly sealed containers to prevent leakage and contamination. It should be transported according to standard chemical handling regulations, preferably at room temperature, away from heat, flames, and incompatible substances. Proper labeling, documentation, and protective packaging are required to ensure safe delivery and storage.
    Storage 2-Benzofurancarboxylic Acid Ethyl Ester should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect the chemical from light and moisture. Ensure the storage area is equipped with proper spill containment and clearly labeled. Follow standard laboratory safety and handling guidelines.
    Application of 2-Benzofurancarboxylic Acid Ethyl Ester

    Applications of 2-Benzofurancarboxylic Acid Ethyl Ester in Industrial Manufacturing

    As a specialized producer of 2-Benzofurancarboxylic Acid Ethyl Ester, we supply this compound as a targeted intermediate for multiple advanced chemical manufacturing domains. Our material supports diverse sectors that demand tightly controlled synthesis routes, high purity, and traceable regulatory compliance across distinct downstream processes.

    1. Pharmaceutical Intermediate for Benzofuran-Based APIs

    Major pharmaceutical companies incorporate this ester as a crucial intermediate in multi-step syntheses of specific benzofuran-derived active pharmaceutical ingredients. It acts as a protected carboxylic precursor within proprietary routes, particularly in anti-arrhythmic and neuroprotective drug R&D pipelines. The compound integrates during intermediate-stage transformations and undergoes further functional group manipulations before deprotection, ensuring regulatory traceability and batch purity.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. relevant monographs for intermediates
    • 21 CFR Part 211 (FDA) for process controls and traceability
    • EU Directive 2001/83/EC for medicinal product supply chains

    Typical usage ratio

    • Used as 1.0 to 1.15 molar equivalents depending on downstream acylation or reduction steps
    • Manufacturers calculate the input based on theoretical yield and allowed process loss, adjusted per batch protocol

    Downstream process integration

    • Introduced at the protected acylation step after initial benzofuran ring formation
    • Feeds directly to subsequent saponification, reduction, or cross-coupling stages
    • Subject to in-process HPLC purity checks before further conversion
    • Stage-specific handling to prevent contamination or hydrolysis before deprotection

    Final product types

    • Anti-arrhythmic drug raw intermediates
    • Benzofuran-based neuroprotective agents
    • Intermediates for non-steroidal anti-inflammatory drugs (NSAIDs) synthesis
    • Building blocks for proprietary API candidates

    2. Agrochemical Synthesis of Benzofuran-Linked Fungicides

    Global agrochemical formulators use this compound as a building block when manufacturing next-generation fungicides containing benzofuran motifs. The ester group enables selective transesterification or hydrolysis, providing synthetic flexibility in producing active substance cores. It enters the pipeline during targeted synthetic steps and supports stringent agricultural product standards, including residue and purity thresholds.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (JMPS)
    • OECD Series on Pesticides Testing and Assessment
    • ISO 9001:2015 quality management for agrochemical production
    • REACH registration (EC No. 1907/2006) for European supply

    Typical usage ratio

    • Typical loading ranges from 0.8 to 1.2 molar equivalent in alkylation or condensation reactions depending on downstream targets
    • Dosage calculated according to pilot trials and scale-up yields, always referenced to desired actives purity

    Downstream process integration

    • Fed into condensation or cyclization step post-fluorination or halogenation
    • Under controlled pH and temperature to ensure ester stability
    • Intermediate isolated and characterized by GC-MS and NMR before next phase
    • Downstream hydrolysis or amide formation before final formulation

    Final product types

    • Benzofuran-based fungicide actives
    • Crop protection intermediates
    • Pre-mix components for seed coating formulations
    • Specialty pesticide ingredient blends

    3. Performance Material Synthesis for Specialty Dyes & Pigments

    The fine chemicals sector applies this ester as a functional intermediate during the development of advanced benzofuran-derived pigments used in technical coatings, electronic inks, and specialty plastics. The ester’s reactivity ensures precise tailoring of pigment backbones, facilitating controlled ester hydrolysis, oxidation, or cross-coupling. Our QC documentation supports traceability required for advanced colorant applications in industrial products.

    Industry compliance standards

    • ISO 9001/14001 for pigment manufacturing and environmental controls
    • EN 71-3: Safety of Toys – Migration of Certain Elements (for plastics and inks)
    • ASTM D4303: Lightfastness of Colorants
    • RoHS Directive (2015/863/EU) for electronics-related applications

    Typical usage ratio

    • Loading typically 0.75 to 1.05 molar equivalents relative to ring construction units
    • Adjustable according to required shade, pigment strength, and reaction scale

    Downstream process integration

    • Used in early synthesis of chromophore backbone
    • Processed under solvent-controlled conditions to manipulate ester group prior to further functionalization
    • Supports downstream sulfonation, chlorine substitution, or coupling reactions
    • Batch lots analyzed by UV-Vis and HPLC to confirm intermediate specifications

    Final product types

    • Industrial benzofuran-based pigments for coatings
    • Specialty dyes for technical printing inks
    • Color masterbatches for engineering plastics
    • Optoelectronic pigment dispersions (e.g., for conductive inks)

    4. Electronic Chemical Synthesis in OLED Active Layer Materials

    Display and electronics manufacturers leverage this ester as a starting material in the preparative routes for benzofuran-based OLED emitter or hole-transport compounds. The molecule enters multi-step syntheses requiring strict control of electronic properties and impurity levels. Our facility delivers these intermediates in compliance with electronics industry validation, supporting scalable OLED fabrication through both batch and continuous-flow processes.

    Industry compliance standards

    • ISO 9001:2015 for electronic chemical production
    • IPC-5704: Cleanliness Requirements for Unpopulated Printed Boards
    • RoHS compliance (Restriction of Hazardous Substances)
    • REACH registration for import/export within the EU market

    Typical usage ratio

    • Introduced at 1.0 to 1.10 molar ratio relative to other monomers in coupling reactions
    • Process engineers may adjust up to 1.2 equivalents depending on desired molecular weight and device specification

    Downstream process integration

    • Deployed after initial aromatic substitution, serving as a protected carboxyl group donor
    • Hydrolyzed under anhydrous or mild alkaline conditions to prevent loss of function groups
    • Purity checked via LC-MS and GC analysis to meet device-grade material standards
    • Feeds to final coupling, amidation, or polymerization steps for OLED stack segment production

    Final product types

    • OLED small molecule emitters with benzofuran structure
    • Hole-transport material intermediates
    • Electroluminescent materials for flexible and rigid display manufacturing
    • Specialty charge-transport additives for advanced display R&D
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    Certification & Compliance
    More Introduction

    2-Benzofurancarboxylic Acid Ethyl Ester: Practical Insights from a Chemical Manufacturer

    A Close Look at 2-Benzofurancarboxylic Acid Ethyl Ester

    As a chemical manufacturer with years spent refining aromatic compounds, we value clarity when introducing a product like 2-Benzofurancarboxylic Acid Ethyl Ester. This specialized ester, based on the benzofuran framework, continues to draw steady demand from pharmaceutical research, specialty chemical synthesis, and agrochemical industries looking for reliable intermediate options. Over time, we have focused on producing this compound with consistency, knowing that its purity directly impacts downstream applications.

    The structure of 2-Benzofurancarboxylic Acid Ethyl Ester gives it a unique position among aromatic esters. Its core features a benzofuran ring bonded to an ethyl ester group at the second position, striking a balance between reactivity and resistance to hydrolysis. This balance makes it easy to handle in bench-scale or pilot-scale settings. With a molecular formula of C11H10O3, it slots into a mid-range molecular weight bracket that facilitates transport and storage without major hassles. Our in-house methodology focuses on minimizing impurities and residual solvents, so chemists can start from a dependable base.

    Model and Specifications Driven by Real-World Experience

    Chemical manufacturers often encounter discrepancies between laboratory grades and bulk quantities. 2-Benzofurancarboxylic Acid Ethyl Ester serves best in well-defined grades—our standard model offers greater than 99% purity by HPLC. We see that color, odor, and residue thresholds are more than just numbers. Formulation chemists and synthesis specialists rely on these figures to determine stepwise yields, so we have tailored our filtration and crystallization methods accordingly.

    Our batches undergo regular GC-MS analysis. Water content stays below 0.2% w/w, a level reached by vacuum drying techniques that prevent the ester from picking up moisture in humid warehouse environments. We have absorbed plenty of lessons about glass bottle vs. HDPE drum performance, noting that certain storage materials interact with the dry ester over extended periods. We recommend amber glass bottles for smaller volumes, giving extra protection from UV exposure and oxidation, while larger customers have benefited from lined steel drums in controlled warehouses. Customers often report improved shelf life under these storage conditions.

    Applications: Usability for Today’s Synthesis

    Most inquiries for this ester come from medicinal chemistry and agrochemical R&D, though we also notice a rising trend from industrial pigment manufacturers. During consultation with technical teams, we find that this compound’s utility as a building block rests in its activated benzofuran nucleus and accessible ester function. Saponification reactions allow rapid generation of the free acid, supporting the development of anti-inflammatory agents and heterocyclic libraries.

    We have worked with researchers optimizing synthetic routes for new API candidates, using 2-Benzofurancarboxylic Acid Ethyl Ester as an intermediate en route to fused tricyclic compounds. The ethyl ester releases under controlled basic conditions, giving researchers flexibility with downstream amide coupling steps. In cases where purity levels dip, we see notable losses at the hydrolysis stage, confirming the importance of clean feedstocks for scalable medicinal chemistry. Synthesis teams often mention reduced side-product formation compared to methyl ester analogues—with the ethyl moiety bringing the right balance of volatility and selective reactivity.

    Contract researchers tasked with supplying kilogram lots for pre-clinical studies routinely choose this ester in place of free acids, due to improved handling and solubility in typical organic solvents like dichloromethane and ethyl acetate. We receive feedback about its rapid dissolution and the ease of filtration, even at larger scales where filtration clogging can slow a project timeline. In pigment research labs, the ester plays a role in creating new dye precursors by yielding benzofuran-based chromophores with enhanced photostability.

    The Value of Purity and Traceability in Every Batch

    Chemical processes demand trust in raw materials. Real-world synthesis rarely matches idealized reaction schemes, so we keep focus on clear documentation and chain-of-custody in every production run. By using high-quality feedstocks and tightly controlled esterification steps, our 2-Benzofurancarboxylic Acid Ethyl Ester offers reliable batch-to-batch purity. Analytical reports accompany all shipments, so recipients can trace their results back to a specific lot, increasing reproducibility in both academic and industrial research.

    Occasionally, we see requests for customized particle sizes. While the ester demonstrates solid stability, some researchers seeking high-throughput workflows prefer a crystalline powder with defined size ranges. We use sieving and milling techniques to supply either fine or coarse fractions, depending on the recipient’s equipment and process requirements. Customer feedback shows that controlled particle sizing simplifies dispersion in solvent systems, saving valuable time during initial screenings.

    For those managing hazardous waste, we note that 2-Benzofurancarboxylic Acid Ethyl Ester leaves less environmental residue compared to certain chloro- or nitroaromatic esters. Our disposal analyses show low ecotoxicity when handled per established regulations. We often lead training sessions for customer site safety teams to reinforce responsible handling and disposal practices.

    Where 2-Benzofurancarboxylic Acid Ethyl Ester Stands Apart

    Comparing chemical intermediates involves more than analytical specs. Many R&D teams used to work with the common 2-benzofurancarboxylic acid methyl ester and toluene analogues, only to face drawbacks with those alternatives. In our experience, the methyl ester’s volatility poses risks during flash evaporation or distillation—raising potential for losses and contamination of condensate lines. Customers often come to us after dealing with repeated inconsistencies in methyl ester content, leading to variable yields in their target products.

    Our ethyl ester form offers greater thermal stability, keeping evaporation and handling hazards to a minimum, especially in open systems where ventilation is strong but solvent recovery dominates concerns. With this in mind, pharmaceutical partners have documented steadier downstream performance. On the other hand, carboxylic acids themselves absorb water quickly, tending to clump and produce unwanted hydrolysates on the shelf. The ethyl ester’s resistance to ambient moisture lets labs store this intermediate for longer periods—sometimes up to 18 months in controlled environments—without performance drift.

    Looking at broader alternatives, some groups use the corresponding amide or chloride derivatives for coupling reactions, but these require harsher synthesis conditions or pose additional transport challenges under strict regulatory frameworks. The ester’s moderate reactivity bridges the gap between synthetic flexibility and safe, compliant shipment. Compared to halogenated intermediates, 2-Benzofurancarboxylic Acid Ethyl Ester sidesteps many costly transport codes, resulting in fewer regulatory delays or surcharges for international shipments.

    Supporting Discovery and Scale-Up Projects with Our Experience

    Bringing a compound from grams to kilogram quantities brings its own set of practical hurdles. Researchers who move up to pilot plant scale need assurances that a supplier’s processes can scale reliably. We produce this ester in reactors certified for pharmaceutical ingredient manufacture, tracking each input and adjusting agitation and temperature control to ensure uniformity throughout the batch. Scale-up customers often mention the value in being able to order from the same source through successive project phases, eliminating compatibility checks each time numbers change.

    During major supply disruptions, such as pandemics or natural disasters, laboratories see delays when their chemical intermediates come from traders or resellers with little production transparency. By working directly with facilities that hold raw material stock and operate distillation units on-site, clients avoid these headaches. They get access to real-time inventory updates and can negotiate directly for emergency shipments. Our long-term partners highlight how this direct access improves their own project lead times.

    Large synthesis projects, especially those generating reference libraries for AI-driven drug discovery platforms, demand not just reliable quality but consistent timelines. Having invested in automated monitoring for reaction endpoints and solvent recoveries, our teams identify and address process variations before they can affect delivery schedules. Feedback from late-phase development groups confirms that this stability carries through from gram-scale piloting to multi-kilogram lots, lowering the risk of unexpected deviations in their process validation runs.

    Environmental and Regulatory Considerations From Our Perspective

    Customers frequently ask about the sustainability of our aromatic esters—an issue that has come to the fore as environmental regulations grow more stringent. This compound stems from a batch-esterification process using widely available, lower-toxicity reagents. Outgassing and effluent levels meet the current requirements set by regional authorities, with most emissions scrubbed or condensed for safe disposal.

    We note that some related intermediates, like certain nitro- or halogenated benzoic esters, need additional compliance steps through dedicated hazardous goods infrastructure. With 2-Benzofurancarboxylic Acid Ethyl Ester, downstream applications avoid added regulatory reporting found with more active halogenated benzofuran compounds, helping keep projects within both time and budget constraints. Our team works with logistics and regulatory advisors to track shifting requirements for labeling, documentation, and regional chemical safety notifications, passing relevant updates directly to our customers.

    Waste streams from typical laboratory-scale use remain manageable, owing to relatively low toxicity and high conversion rates in target syntheses. We support research groups with advice drawn from our own housekeeping practices, such as routine pH-neutralization and incineration for spent solvent mixtures. This exchange of operational knowledge empowers end-users to adopt similar procedures, easing the burden on local environmental agencies and internal audits.

    Lessons from Real-World Handling and Customer Collaboration

    Every time we ship a batch of our 2-Benzofurancarboxylic Acid Ethyl Ester, we are reminded that a product’s success rides on supporting both straightforward and complex workflows. On several occasions, clients have run side-by-side process trials with competitors’ esters, noting the impact of small differences in melting points, crystal habit, or solubility characteristics. One medicinal chemistry lab reported that our ester shortened total process time in ester hydrolysis and acid re-crystallization, cutting labor hours and reducing loss during workup.

    Handling inquiries from pigment and dye manufacturers, we see that subtle differences in the starting ester control the color purity in finished chromophores. Their feedback underscores the need for a tightly monitored process, as even trace byproducts can impart unwanted hues in downstream products. These conversations spurred us to integrate extra filtration and clarify steps along our esterification route.

    In larger consignment orders, we collaborate directly with technical buyers looking for value in the supply chain. Some prefer resin-lined drums, others require eco-friendly transport packaging—the key remains adapting to the specific needs, grounded in logistics experience and feedback from the shipping floor. Real-time communication between production, shipping, and customer tech teams closes the loop and streamlines each transaction.

    The Role of Direct Chemist-to-Chemist Dialogue

    Manufacturing specialty chemicals is not just about filling orders. Experienced process chemists who receive direct input from users deliver more fit-for-purpose materials. We have refined our crystal form and filtration methods based on direct field reports from R&D teams. This chemist-to-chemist dialogue encourages open sharing of on-the-job knowledge, which leads to measurable improvements in reactivity and storage stability.

    Sometimes chemists ask us to tailor specific lot sizes to their synthetic set-ups. Smaller research groups often struggle with minimum order quantities from commodity sources, leading to excess waste or unnecessary cost. By offering flexible packaging—ranging from milligram vials for screening tasks up to custom multi-kilogram containers—we support projects of any scale, and adjust our cleaning protocols accordingly for each product configuration.

    Technical support extends beyond written guidelines. Our teams routinely respond to troubleshooting requests around the world, helping to pinpoint the source of purification losses or unexpected chromatographic traces. This approach ensures that research groups always have the most up-to-date handling advice as conditions change. A two-way relationship creates a cycle of improvement, benefiting both supplier and client.

    Preparing for Future Research with Practical Products

    As innovation evolves, demands on chemical intermediates intensify. High-throughput screening, combinatorial synthesis, AI-assisted drug development, and advanced materials research all place greater value on reliable, pure, and accessible intermediates. We continue to invest in new reaction control systems, analytical tools, and storage solutions for 2-Benzofurancarboxylic Acid Ethyl Ester, anticipating how research workflows will shift over time.

    By drawing from an archive of both customer feedback and in-house testing, we expect this ester to retain its place as a cornerstone intermediate for benzofuran-based projects. Close monitoring of emerging standards in pharmaceutical, environmental, and specialty material fields helps us prepare to meet future requirements, whether those involve new documentation regimes, stricter purity thresholds, or even bio-based approaches to aromatic ester production.

    Our direct experience shapes every batch, every customer conversation, and every improvement along the way. The knowledge we gain from day-to-day problem-solving not only ensures that 2-Benzofurancarboxylic Acid Ethyl Ester stays relevant, but also supports the wider community of chemists as research challenges continue to grow in complexity.