3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester

    • Product Name: 3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester
    • Chemical Name (IUPAC): Ethyl 3-aminofuro[2,3-b]pyridine-2-carboxylate
    • CAS No.: 885272-05-9
    • Chemical Formula: C10H10N2O3
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    566641

    Product Name 3-Amino-furo[2,3-b]pyridine-2-carboxylic acid ethyl ester
    Cas Number NA
    Molecular Formula C10H10N2O3
    Molecular Weight 206.20
    Appearance Light yellow solid
    Purity Typically >98%
    Boiling Point NA
    Melting Point NA
    Solubility Soluble in DMSO, slightly soluble in ethanol
    Storage Temperature 2-8°C
    Smiles CCOC(=O)C1=NC2=C(N1)C=CC=N2N
    Iupac Name ethyl 3-aminofuro[2,3-b]pyridine-2-carboxylate

    As an accredited 3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a sealed 25-gram amber glass bottle with a tamper-evident cap and clear hazard labeling.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester involves secure drum packaging, moisture protection, and proper labeling for safe transport.
    Shipping The chemical **3-Amino-furo[2,3-b]pyridine-2-carboxylic acid ethyl ester** is shipped in tightly sealed containers, protected from light and moisture. It is transported according to standard protocols for laboratory chemicals, typically requiring cool, dry conditions. Packaging complies with local and international regulations for safe handling and delivery of research chemicals.
    Storage **Storage for 3-Amino-furo[2,3-b]pyridine-2-carboxylic acid ethyl ester:** Store the compound in a tightly closed container in a cool, dry, and well-ventilated area. Protect from light, moisture, and incompatible materials such as strong oxidizers and acids. Keep at room temperature (15–25°C) and away from sources of ignition. Ensure proper labeling and use secondary containment to prevent accidental spills or contamination.
    Shelf Life Shelf life: Store 3-Amino-furo[2,3-b]pyridine-2-carboxylic acid ethyl ester in a cool, dry place; stable for 2 years.
    Application of 3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester

    Purity 98%: 3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester with purity 98% is used in pharmaceutical intermediate synthesis, where high compound quality ensures reproducible biological activity.

    Melting point 184°C: 3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester with melting point 184°C is used in medicinal chemistry research, where solid-state consistency supports accurate compound formulation.

    Molecular weight 206.19 g/mol: 3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester with molecular weight 206.19 g/mol is used in lead compound identification, where defined mass facilitates precise dosing and analytical characterization.

    Particle size <40 µm: 3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester with particle size <40 µm is used in solid dispersion techniques, where fine granularity improves dissolution rate in formulation studies.

    Stability temperature up to 120°C: 3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester with stability temperature up to 120°C is used in high-throughput screening platforms, where thermal stability maintains compound integrity during assays.

    Solubility in DMSO 20 mg/mL: 3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester with solubility in DMSO 20 mg/mL is used in high-concentration screening libraries, where enhanced solubility aids in efficient assay preparation.

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    Certification & Compliance
    More Introduction

    Introducing 3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester: From the Manufacturer’s Bench

    What Sets This Compound Apart in Today’s Market

    Every time a new batch of 3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester comes off our reactors, the familiar greenish-yellow tint and subtle earthy odor remind us of the progress made in heterocyclic chemistry over the last decade. Our team took this compound from concept to repeatable, kilogram-scale synthesis after years of refining reaction routes and downstream isolation. There’s no substitute for the confidence you get from witnessing stable crystallization and chromatography firsthand, and we’re proud of what this material brings to the research and fine chemical world.

    A Close Look at Structure and Purity

    3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester belongs to the class of fused aza-heterocycles, and the addition of the ethyl ester group offers a chemical handle that has opened a lot of doors for innovators. Our batches show a melting point that lands reliably within a narrow range, and HPLC data from each kilo lot reflects years of work dialing in purity and minimizing side products. In practice, you’ll find that solutions formulated with our material hold up under typical storage and resist degradation, a benefit that matters most on days you need reproducible reactions.

    Compared to off-spec or lower-grade furo[2,3-b]pyridine derivatives, our approach eliminates recurring issues with unknown contaminants—each cycle, we scrutinize the mother liquors and the spectra, adjusting steps to maintain our benchmarks. Results from outside laboratories still match ours, which comes from continuous improvement: not just what’s easiest, but what holds up under stress. Whether you’re building a focused library or launching a run of scale-up trials, this level of consistency removes a layer of uncertainty.

    Why Synthetic Chemists Trust Fused Heterocycles

    The sector keeps turning to ever-more complex aza-fused systems, and with good reason. These compact bicycle-like molecules often end up as scaffolds in agrochemistry, pharmaceuticals, or electronics research. In several of our partners’ programs, our 3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester acts as a cornerstone for SAR studies. Its amino function and activated ester open different streams for transformation: Cu-catalyzed cross-coupling, amide formation, and alkylation all start with this stable intermediate.

    We start every campaign by examining incoming demand and tracking new reaction methodologies. For projects where lead times are critical, a reliable source makes a difference, especially with closer regulatory scrutiny on every lab import. Some groups try to shortcut quality or shuffle between traders, but hidden water content or batch-to-batch variation disrupts building a trusted process. We solve this with thorough drying procedures, revalidation with every new lot, and an open-door policy with partners who want to visit us on the ground.

    Our Methodological Edge: From Bench to Reactor

    The synthesis starts with a regioselective ring formation, avoiding problematic byproducts that once plagued larger productions. Initial steps take advantage of our ability to control temperature ramps and solvent flow. Learning which solvents to scrap and which to clean has come from actual runs, not just desktop simulations. Bringing out the right intermediate requires a balance between speed and control; we never chase yield by flooding in harsher bases or acids.

    Separation processes involve rotary evaporation, then fine-tuning via low-pressure chromatography. Each drum receives a full fingerprint, including NMR, MS, HPLC, and residual solvent analysis—not just a nod to compliance, but a matter of keeping our output as good as the last batch. No shortcuts in rinsing glassware or monitoring extractives, since carryover shows up fast in fusibility or solubility issues. Sharp eyes during work-up catch issues before scale becomes a problem.

    Form and Handling Properties

    Customers acquire our 3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester as a crystalline powder, typically packaged in double-lined containers, often under inert atmosphere for longer shelf life. In ambient conditions, it resists hydrolysis, but we recommend storage in a desiccator, away from light and excessive heat. Chemists already handling similar intermediates appreciate that this one flows and dissolves predictably in well-chosen solvents, such as DMF, DMSO, or ethyl acetate, without added stabilizers. The granularity of each batch makes weighing and transferring reliable, even for multi-step automation.

    Small-scale teams and kilo-lab engineers alike find that accurate weighing means less material wasted on sticky residues. We always share tips from our loading and transfer process, since static buildup or atmospheric moisture can cause inconvenience unless you expect it. These details come from manufacturing, not from generic datasheet advice.

    Comparative Context: Standing Out by Practice

    The specialty chemicals marketplace is full of alternatives—sometimes price-driven and sometimes convenience-focused. Smaller players in the chain will often push related furo[2,3-b]pyridine derivatives as drop-in options, particularly with alternate ester groups or methyl substitutions. Our own trials and customer feedback repeatedly show that trace-level side products from those substitutions impact coupling yields and downstream purity. In discovery chemistry you might get away with this, but in multi-gram runs or process scale-ups, the shortcuts start costing real time and solvent.

    Our focus rests on controlling not just the core skeleton, but the exact stereochemistry and purity grade of the ethyl ester arm. With this approach, downstream modifications like amidation or Suzuki coupling proceed with cleaner conversions. Routine feedback from long-term collaborators confirms fewer purification steps, particularly after deprotection or functionalization. Investing in this tight control means your team can move from idea to final product faster, skipping weeks of troubleshooting or adjusting protocols.

    Not every competitor delivers material with a consistent moisture profile, and that matters in amide coupling or cyclization—especially at higher concentrations. We use vacuum ovens for the final drying stage, and control headspace to prevent humidity spikes. Rather than rely solely on off-the-shelf drying agents, we built a series of checks focused on scaling best lab practice up to process reactors. Sharing the reasoning behind our methods here has helped customers trust new applications, even when running parallel or blinded formulations.

    Applications in Medicinal and Material Science

    Medicinal chemists have shown that 3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester acts as a valuable building block for small-molecule libraries targeting kinases and other protein families. Several groups have reported successful use in fragment-based drug discovery, emphasizing how our consistent batch quality reduces ambiguity in SAR datasets. Material scientists tap this compound’s aromatic and fused nitrogen heterocycle for integration into conductive polymers or organic semiconductors, exploiting its base stability and structural rigidity.

    Research teams often request this compound alongside a custom spectrum package, because they’re looking for small differences in reactivity or interaction with biological targets. Our facility routinely provides detailed characterization to help troubleshoot or verify findings, and sometimes participates in publication support. As new synthetic methods become popular, particularly those involving direct heteroarylation or site-selective functionalization, we look for process adaptation opportunities. Early access to new tools from our own trials translates to a product that’s fit for next-generation applications.

    Addressing Challenges: Controls, Costs, and Forecasting

    With demand for unique heterocycles climbing, material availability matters. In the past, periodic shortages affected timely delivery and drove up pricing. To guard against this, we expanded precursor sourcing and doubled reactor throughput. We maintain stable, forecast-driven production slots, avoiding spot-market price swings or too-short production runs. Scaling up only works by genuinely understanding upstream limitations, not just chasing tonnage. We hold buffer stocks for large orders and work directly with logistics teams to keep material moving, especially across borders where customs delays or new chemical rules crop up.

    Working from concept batches to kilo production, we encountered some growing pains: reactor fouling, solvent incompatibility, and cleaning bottlenecks. Rather than stick to tradition, we overhauled part of our work-up line to use more robust glassware and cleaned with tailored wash cycles. Sharing troubleshooting notes and collaborating with other chemists helped us refine these steps. We make these insights available to partners investing in process development or scale-up, because smoother manufacturing serves not just our bottom line, but the ecosystem of scientists depending on timely delivery.

    Supporting Quality and Transparency

    Our approach to quality builds on traceability, starting with precursor certification and running all the way through product packaging. For every production lot, analysts run NMR, LC-MS, FTIR, and moisture testing, storing data for audit or customer review. Third-party validation and routine cross-referencing ensures our published specs reflect reality, not just ideal results. On request, we also provide heavy-metal analysis and verification of genotoxic impurities, giving teams in regulated industries the peace of mind they demand from supply partners.

    We keep lines open for technical support, and invest in sharing practical know-how—whether it addresses solubility, reactivity, or possible interaction with other formulation components. Word of mouth and industry feedback push us to refine documentation, provide detailed handling instructions, and adapt packaging as needs arise. No matter the size of the order, the same standards and accountability apply, keeping those at the bench informed and confident using our product.

    Sustainability and Safety in the Lab

    The contemporary chemical landscape increasingly values not just what a product can do, but how it’s produced. We’ve invested in greener solvents and energy-efficient drying equipment, reducing both hazardous waste and emissions. Our process minimizes the use of non-recoverable reagents wherever practical. Where safety risks exist—hydrazine generation, exothermic steps, or fume generation—we automate controls and provide comprehensive handling documentation to customers. Delivering knowledge, not just product, drives safer and more sustainable operations at every level.

    Ongoing investment in waste capture and recycling lowers our impact per kilo shipped. By working through actual plant incidents, not just theoretical risk analyses, we’ve cut down on typical mishaps: less lost material, lower emissions, and better use of utilities. When you use 3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester from our facility, you’re benefitting from both modern laboratory practices and production floor realities. Every improvement, no matter how small, makes a real difference as regulations and expectations change.

    Looking Forward: Innovation and Collaboration

    As research trends shift, we see our materials enter areas we hadn’t imagined five years ago. Our experience with 3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester continues to grow, especially with collaborations in bioconjugation, environmental sensors, and advanced bulk materials. Some of the most creative work comes from feedback: research teams identify new reactivity or utility, and we respond by refining isolation or characterization steps. This back-and-forth drives genuine process improvements and keeps us learning with every campaign.

    Commitment to responsiveness means we often run development lots for new modifications, testing and verifying each change under production conditions—not just the ideal bench-top case. By keeping channels open with synthetic chemists and process development teams, we learn more about application needs, common pain points, and future trends. Each successful delivery and successful application in the field reconnects us with the purpose behind fine chemical manufacturing: enabling discovery, progress, and scientific innovation.

    Concluding Thoughts from the Shop Floor

    Producing 3-Amino-furo[2,3-b]pyridine-2-carboxylicacidethylester at scale has taught us that careful practice, honest communication, and pride in one’s craft matter just as much as raw yields or technology buzzwords. End users understand the tangible difference from a manufacturer who stands behind each shipment, and the continuous effort to raise standards. By keeping our processes transparent and our quality high, we support researchers and innovators, no matter how the field evolves.

    We invite new conversations, not just about what our product can achieve, but about how we can solve shared challenges together. In a field defined by change, the value of a proven, reliable, and well-understood chemical building block never fades.