2-{[(furan-2-yl)methyl]sulfanyl}pyridine

    • Product Name: 2-{[(furan-2-yl)methyl]sulfanyl}pyridine
    • Chemical Name (IUPAC): 2-[(furan-2-ylmethyl)sulfanyl]pyridine
    • CAS No.: 39293-97-1
    • Chemical Formula: C10H9NOS
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    749402

    Iupac Name 2-{[(furan-2-yl)methyl]sulfanyl}pyridine
    Molecular Formula C10H9NOS
    Molecular Weight 191.25 g/mol
    Cas Number 84110-09-8
    Appearance Light yellow to brown liquid
    Boiling Point Estimated ~290°C
    Density 1.21 g/cm³ (estimated)
    Solubility In Water Slightly soluble
    Smiles C1=CSC(=C1)CSC2=NC=CC=C2
    Inchi InChI=1S/C10H9NOS/c1-2-10(13-6-1)7-12-9-5-3-4-8-11-9/h1-6,8H,7H2
    Pubchem Cid 199732
    Refractive Index 1.584 (estimated)
    Logp 2.13 (estimated)

    As an accredited 2-{[(furan-2-yl)methyl]sulfanyl}pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 5 grams, sealed with a screw cap, labeled with product name, CAS number, and hazard information.
    Container Loading (20′ FCL) 20′ FCL container loading for 2-{[(furan-2-yl)methyl]sulfanyl}pyridine ensures efficient, secure bulk shipment with optimized space and protection.
    Shipping 2-{[(Furan-2-yl)methyl]sulfanyl}pyridine is shipped in tightly sealed containers to prevent moisture ingress and contamination. It is packaged according to international chemical transport regulations, labeled appropriately, and cushioned to avoid breakage. Handling includes temperature and light protection, conforming to standard safety and hazardous material shipping guidelines.
    Storage 2-{[(Furan-2-yl)methyl]sulfanyl}pyridine should be stored in a tightly sealed container under a dry, inert atmosphere, such as nitrogen or argon, to prevent moisture and air exposure. Keep it in a cool, well-ventilated chemical storage area, away from heat, ignition sources, and incompatible substances like oxidizers. Store at room temperature or as indicated on the supplier’s label.
    Shelf Life 2-{[(Furan-2-yl)methyl]sulfanyl}pyridine typically has a shelf life of 2 years when stored cool, dry, and protected from light.
    Application of 2-{[(furan-2-yl)methyl]sulfanyl}pyridine

    Purity 98%: 2-{[(furan-2-yl)methyl]sulfanyl}pyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where high-purity enables reproducible batch processing.

    Melting Point 62°C: 2-{[(furan-2-yl)methyl]sulfanyl}pyridine with a melting point of 62°C is used in agrochemical formulation, where controlled melting facilitates uniform dispersion.

    Molecular Weight 205.28 g/mol: 2-{[(furan-2-yl)methyl]sulfanyl}pyridine at a molecular weight of 205.28 g/mol is used in heterocyclic compound libraries, where accurate mass allows precise compound identification.

    Stability Temperature up to 120°C: 2-{[(furan-2-yl)methyl]sulfanyl}pyridine with stability up to 120°C is used in organic electronics research, where thermal stability maintains performance under processing conditions.

    Particle Size <50 μm: 2-{[(furan-2-yl)methyl]sulfanyl}pyridine with particle size below 50 μm is used in high-throughput screening assays, where fine sizing enhances reaction kinetics and solubility.

    Solubility in DMSO 100 mg/mL: 2-{[(furan-2-yl)methyl]sulfanyl}pyridine with solubility of 100 mg/mL in DMSO is used in medicinal chemistry assays, where high solubility supports concentrated stock solutions.

    HPLC Assay ≥99%: 2-{[(furan-2-yl)methyl]sulfanyl}pyridine with HPLC assay not less than 99% is used in analytical reference standards, where assay precision ensures data reliability.

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    Certification & Compliance
    More Introduction

    Introducing 2-{[(furan-2-yl)methyl]sulfanyl}pyridine: Practical Insights from Our Own Manufacturing Experience

    A Look at 2-{[(furan-2-yl)methyl]sulfanyl}pyridine

    Stepping into the day-to-day work of chemical synthesis, eventually you run into compounds that challenge your expectations and reshape your sense of chemical reactivity. 2-{[(furan-2-yl)methyl]sulfanyl}pyridine has been a good example of that for us. Its structure brings together the characteristic reactivity of pyridine with the electron-rich, heterocyclic nuances of a furan ring, linked through a robust thioether bridge. This combination opens possibilities, both in the lab and at industrial scale. Our team has become very familiar with its quirks and performance, not just in the catalog but lined up on the reactor floor or under the scrutiny of GC-MS and NMR.

    Core Specifications: Beyond the Basics

    Behind every batch of 2-{[(furan-2-yl)methyl]sulfanyl}pyridine lies a practical understanding of both purity and consistency. Our typical offering provides this material at purities exceeding 98% (HPLC-tested), with moisture levels controlled below 0.5%. Residual solvents fall beneath quantifiable thresholds as monitored by headspace GC. Appearance is a pale yellow to yellow oily liquid under normal conditions, sometimes with a faint earthy odor, which is characteristic for sulfur-bearing organics. Our containers use dark glass to minimize light exposure, as both the furan and pyridine motifs may show mild photo-reactivity over time; this storage step traces back to experiences with slight color shifts on bulk storage.

    Each production lot tracks both sulfur and nitrogen content by elemental analysis, with observed values closely matching theoretical predictions. Over the years, we have found that running regular ^1H NMR checks spot minor impurities more reliably than relying on a single purification step—subtle side products can creep in, especially with less controlled exotherms during alkylation. This has led us to refine both the cooling cycle and the base selection during synthesis. Packing the product for shipment, we never overlook peroxide monitoring, since trace peroxides can accumulate in the presence of air and traces of light, even when theoretically unlikely.

    Why Use This Compound?

    Labs and commercial users have asked what draws our focus to this particular structure. It all comes down to the interplay of electronic and steric effects. The sulfur atom introduces a certain flexibility into the molecule, making it compatible with a diverse set of transformations: cross-coupling, ligand development, organometallic studies, and more. The furan ring brings planar aromaticity and some acid sensitivity, while the methyl group tethers the two heterocycles just far enough apart to prevent intramolecular deactivation.

    From direct experience, we have seen labs use this compound as a precursor for palladium-catalyzed C-S or C-N bond formation. It often serves as a starting point for the construction of more elaborate ligands and catalysts, especially where a combination of nitrogen- and sulfur-containing coordination sites is needed. Synthetic teams working on medicinal chemistry projects have, on more than one occasion, reported that its Building block status helps save steps; attaching fragments through that thioether connects units that otherwise demand multi-step protection and deprotection cycles.

    Real-World Comparisons and Key Differences

    It’s tempting to lump 2-{[(furan-2-yl)methyl]sulfanyl}pyridine in with other pyridine derivatives or thioethers, but in our experience, making that shortcut brings surprises. For one, this compound exhibits notably higher solubility in polar aprotic solvents compared to simple alkylthio-pyridines. Unlike quaternized pyridine salts, its neutral state gives it versatility across a range of non-aqueous and slightly acidic conditions. Building blocks like 2-(methylthio)pyridine lack the extended electronic conjugation, so their reactivity differs, particularly in metal–ligand applications. If you’ve worked with furfurylthio derivatives of benzene, you’ll notice a tangibly different behavior here—the electron-withdrawing character of pyridine alters the local environment and, with it, the reaction profiles in both oxidative and reductive settings.

    Within our facility, side-by-side trials have shown that 2-{[(furan-2-yl)methyl]sulfanyl}pyridine offers greater flexibility during ligand optimization stages. It can coordinate with soft metals via sulfur and hard metals through nitrogen, yielding chelation that is both strong and, to some extent, tunable. Unlike bis-thioether compounds, it does not sacrifice the potential for hydrogen bonding through the pyridine core, opening more routes for supramolecular assembly.

    Production and Handling: Practical Lessons from the Plant

    Years in scaled synthesis have taught us the practicalities and pitfalls of making this compound. Sulfides rarely tolerate careless oxidation; the reaction atmosphere—oxygen content, moisture, and even the trace metal content of equipment—strongly influences both yield and downstream purity. We’ve dealt firsthand with batches that needed repurification after minor exposure to air from leaky reactor ports. Temperatures that run too warm too fast during furan alkylation steps tend to increase furan ring opening side products, so strict temperature profiles are in place, and quality checks follow after every shift.

    During distillation, we control pressure manually to avoid product decomposition. Glass-lined vessels remain the default here due to the sensitivity of sulfur- and nitrogen-containing compounds to traditional stainless steel. On occasion, we’ve adapted glass-to-metal transitions with single-use PTFE liners when production demands differ from lab scale to commercial runs.

    Packing requires careful selection; while the compound doesn’t corrode containers as some organosulfur species do, we avoid open transfer to reduce ambient humidity pickup. Over time, our handling practices have evolved through direct observation—visual changes in product suggested fine-tuning of our storage temperature and atmosphere. Samples taken at three, six, and twelve months under different warehouse conditions revealed the best practices, eliminating trial-and-error for our clients and us alike.

    Applications in Synthesis and Discovery

    Chemists appreciate versatility, and 2-{[(furan-2-yl)methyl]sulfanyl}pyridine doesn’t disappoint. Our clients have synthesized metallosupramolecular complexes, bioactive molecules, and functional materials using this compound. In catalysis, it’s served as both a ligand backbone and as a reactive handle for further modifications. Organosulfur compounds like this often find their way into pharmaceuticals, agrochemical intermediates, and material science projects due to their ability to modulate electronic density and provide convenient points for late-stage functionalization.

    One project involved developing switchable ligands for transition metal catalysis; the sulfur and nitrogen pivots were key in tuning both electronic and steric demands. In another case, a medicinal chemistry team used this building block to incorporate both heterocycles in a single scaffold, streamlining SAR (structure-activity relationship) studies in anti-infective research. Other efforts have drawn on its thioether linkage to anchor complex architectures—its chemical stability compared to simple thioethers helped withstand deprotection and metalation steps that are common in lead compound optimization.

    Regulatory Experience and Commitment to Safety

    Having worked through the regulatory landscape for years, we know that documentation and transparency are not just compliance hurdles, but foundations for reliable supply relationships. Each batch comes with full traceability, from raw material selection to final packaging. We maintain batch records with continuous monitoring for REACH and other regulatory requirements. Every lot is tested against established limits for residual solvents, heavy metals, and known genotoxic impurities—this goes beyond industry minimum standards, stemming from a genuine desire to keep everyone, from production colleagues to end users, safe.

    We routinely provide safety data sheets upon request, not as a box-ticking exercise, but because decades in production have demonstrated the value of clear training and understanding of proper handling. There are no shortcuts. Regular hazard analysis, COSHH training, and job-specific PPE—these are the lived realities of plant work, not theoretical ideals. Our firsthand experiences include close-call lessons: never underestimate thioether flammability potential, and always consider cross-reactivity with nearby reagents on multiproduct lines.

    Supporting Reliable Research and Scale-Up

    We’ve heard from more than a few project managers and researchers puzzled by inconsistent supplier quality or unexplained batch-to-batch variation. We take these concerns to heart, drawing upon direct customer feedback and internal investigations. Rather than simply meeting COA numbers, we actively work with clients to support troubleshooting in their applications. Whether collaborating with academic partners scaling up gram-quantities or industry teams running kilo-scale campaigns, we keep testing and improving. Repeat syntheses have led us to refine workup and purification at multiple stages, and those lessons channel back into better product for everyone.

    Control over each production step allows confident supply for pilot- and full-scale manufacturing runs. We perform stability trials and real-world tests—not theoretical computations—so clients can focus on their work, not the reliability of their inputs. The conversation never ends at the point of shipment; ongoing dialogue with end-users often identifies improvements that would never appear in a certification process.

    Innovation—Driven by Experience, Not Guesswork

    It’s easy to talk about innovation in broad strokes, but sustained progress demands attention to lived detail. 2-{[(furan-2-yl)methyl]sulfanyl}pyridine was not just another catalog number for us; it became a proving ground for refining our own process controls and analytical techniques. Reproducible preparation at scale teaches lessons a thousand journal articles never will. Development chemists know real-life side reactions can outflank the neatest mechanistic hypothesis. Persistence in process verification and batch homogeneity built a stronger foundation for further research.

    In response to feedback from materials chemistry groups, we refined our purification protocol to better remove trace halides sometimes left over from the starting pyridine. This attention to detail has, on occasion, required investing in new filtration systems, and we share those insights so customers concentrating their products, or performing downstream derivatization, get consistent outcomes time after time.

    Lessons from the Supply Chain and Sustainability Front

    Supply chain security matters as much as chemical expertise. Over the past several years, disruptions in raw material sourcing—especially for starting furan derivatives—have become more pronounced. Direct manufacturer relationships built over time have guaranteed steady input streams, with backup suppliers vetted for consistent analytical profiles. We sample and analyze all inbound materials prior to acceptance, avoiding costly downstream remediation. By managing the full supply lifecycle, we buffer our partners from market shocks and ensure their research keeps moving forward.

    Our production lines have also adapted to growing expectations around sustainability. Waste minimization, solvent recovery, and by-product valorization became daily practice instead of greenwashing jargon. We actively monitor and optimize our waste streams, capturing sulfur-containing by-products for further conversion, and maximizing raw material utilization throughout each batch. Moving beyond declarations or certifications, these practices have improved operational economy and reduced the burden on local waste management systems.

    Collaborative Support—From Problem Solving to Product Improvement

    As a manufacturer deeply invested in every stage of production, we don’t disappear once an order leaves our facility. Industry collaborations often begin as technical troubleshooting and grow into joint development ventures. Our technical liaisons answer synthesis and scale-up questions backed by real process know-how, not just standard answers or cut-and-paste documentation. In a field where chemical intuition rarely substitutes for hard data, we offer access to full analytical records and detailed process notes when needed.

    Sometimes, new application fields call for altered specifications—higher purity, custom packing, or closer control over trace elements. Rather than approaching these as problems, we take them as opportunities to further refine our process. Our team adjusts, documents, and retests, looping improvements back into future batches.

    Long-Term Reliability—Bench to Bulk

    After years in the industry, it’s clear that customers don’t just order molecules—they rely on partners who deliver experience as well as product. Each kilogram of 2-{[(furan-2-yl)methyl]sulfanyl}pyridine reflects a succession of adjustments, lessons learned from near-misses, and deliberate improvements born of real-world feedback. When clients come back with new questions or requests, those conversations drive the cycle of innovation and refinement.

    As the field grows, so do expectations: greater consistency, deeper documentation, and genuine problem-solving. Our company has never seen chemical manufacturing as a numbers game. Each product stands as the end result of hands-on work, debate, and know-how—the essential groundwork that keeps research and production moving forward without interruption.

    Looking Forward

    The journey with 2-{[(furan-2-yl)methyl]sulfanyl}pyridine serves as a living record of what careful manufacturing, continuous improvement, and collaboration can build. Every lot sent out carries a record of controlled conditions, painstaking documentation, and updates shaped by user input, creating a feedback loop that has raised quality standards and problem-solving capacity.

    All told, experience has shaped our perspective more than protocols ever could. That perspective means we supply not only a dependable chemical, but a partner’s understanding in every bottle.