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Methyl Benzo[B]Thiophene-2-Carboxylate

    • Product Name Methyl Benzo[B]Thiophene-2-Carboxylate
    • Alias 2-(Methoxycarbonyl)benzothiophene
    • Einecs EINECS 410-300-4
    • 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

    150777

    Iupac Name Methyl benzo[b]thiophene-2-carboxylate
    Molecular Formula C10H8O2S
    Molecular Weight 192.24 g/mol
    Cas Number 27841-05-2
    Appearance White to off-white solid
    Melting Point 61-64°C
    Solubility Soluble in organic solvents like DMSO, methanol
    Purity Typically ≥98%
    Smiles COC(=O)C1=CC2=CC=CC=C2S1
    Inchi InChI=1S/C10H8O2S/c1-12-10(11)8-6-7-4-2-3-5-9(7)13-8/h2-6H,1H3
    Storage Temperature Store at room temperature
    Synonyms 2-Carboxy methyl benzo[b]thiophene

    As an accredited Methyl Benzo[B]Thiophene-2-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Opaque amber glass bottle containing 25 grams of Methyl Benzo[B]Thiophene-2-Carboxylate, with screw cap and tamper-evident seal for safety.
    Shipping Methyl Benzo[B]Thiophene-2-Carboxylate should be shipped in tightly sealed containers, protected from light, moisture, and physical damage. Use appropriate labels and documentation in accordance with chemical safety regulations. Transport via recognized courier services for hazardous materials to minimize risk and ensure safe and compliant delivery to the destination.
    Storage Methyl Benzo[B]thiophene-2-carboxylate should be stored in a tightly sealed container, away from direct sunlight, moisture, and incompatible substances such as strong oxidizers. Store it in a cool, dry, and well-ventilated area, ideally in a chemical storage cabinet. Ensure proper labeling, and restrict access to trained personnel. Avoid sources of ignition and handle under appropriate safety protocols.
    Application of Methyl Benzo[B]Thiophene-2-Carboxylate

    Applications of Methyl Benzo[B]Thiophene-2-Carboxylate in Industrial Manufacturing

    Methyl Benzo[B]Thiophene-2-Carboxylate serves as a specialized intermediate across several mature chemical sectors, supporting high-value transformations and advanced syntheses. As the direct manufacturer, we focus on verified application channels where this compound integrates into established downstream processes for pharmaceutical, agrochemical, and material science industries. Below, we highlight each scenario with process-specific insights and regulatory benchmarks.

    1. Pharmaceutical API Synthesis: Heterocyclic Scaffold Construction

    Pharmaceutical development teams value this molecule as a key intermediate in constructing novel heterocyclic cores for active pharmaceutical ingredient (API) candidates, especially for small-molecule drug projects targeting oncology and CNS applications. Chemists use it to yield substituted benzothiophene analogs via ester hydrolysis, amidation, or Suzuki coupling within complex stepwise processes under cGMP conditions. Sourcing consistency and impurity profile control remain critical at this R&D-to-scale transition, supporting DMF filings and investigational drug supply.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP/EP raw material purity specifications
    • FDA and EMA IND filing requirements
    • ISO 9001:2015 Quality Management System

    Typical usage ratio

    • 20–35% molar proportion relative to target scaffold in the early-stage route; adjusted per reaction scale and yield optimization during process validation

    Downstream process integration

    • Introduced at scaffold-forming step, often immediately prior to selective functionalization or ring-closure stages; batch-fed into reaction sequences under controlled temperature and solvent conditions

    Final product types

    • API intermediates for investigational and generic pharmaceuticals
    • Reference standards for clinical research
    • Building blocks for kinase or nuclear receptor inhibitor classes

    2. Agrochemical Active Ingredient Development

    In crop protection R&D, formulators employ this intermediate for constructing benzothiophene-based herbicidal and fungicidal agents. Its unique heterocyclic core enables downstream derivatizations, providing a platform for safer, target-selective crop protection products. Usage must align with regional residue and environmental testing programs; hence, downstream synthesis includes rigorous impurity characterization and scale-up documentation required for field trial registration.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for registration batches
    • REACH Annex VII–X registration provisions
    • FAO and WHO specification for agricultural chemicals
    • ISO 17025 testing for analytical method validation

    Typical usage ratio

    • 5–15% of target synthesis pathway; ratio adjusted according to lead candidate optimization and impurity burden in pilot-scale

    Downstream process integration

    • Charged during early-stage heterocycle assembly; allows functional group modifications to introduce bioactive moieties prior to formation of active ingredients

    Final product types

    • Precursor to selective fungicide actives
    • Synthetic intermediates for post-patent herbicides
    • Key units in combination crop protection formulations

    3. Specialty Dye and Pigment Intermediate

    Methyl Benzo[B]Thiophene-2-Carboxylate provides process chemists in the colorant sector with a platform molecule for preparing high-performance, sulfur-containing dyes used in advanced textile and plastics applications. Its aromatic backbone yields custom chromophore precursors for dyes exhibiting lightfastness and chemical resistance. Downstream production requires monitoring of sulfonation and condensation reactions closely, especially for colorimetry and batch consistency qualification.

    Industry compliance standards

    • EN 71-3 Safety of toys (migration of certain elements in pigments for children's products)
    • OEKO-TEX® Standard 100 for textile dyes
    • GMP for pigments (EC 1223/2009 for cosmetic colorants)
    • ISO 9001 for production batch control and traceability

    Typical usage ratio

    • 10–25% by mass in initial chromophore reaction mixture; fine-tuned by target shade, solubility, and light stability requirements

    Downstream process integration

    • Fed into the first step of chromophore backbone synthesis, followed by post-coupling or condensation for molecular tuning; typically processed via aqueous or solvent extraction depending on end-use sector

    Final product types

    • Aromatic sulfonated dyes for synthetic fibers
    • High-stability colorants for plastic masterbatches
    • Intermediates for printing ink pigment dispersions

    4. Advanced Organic Electronic Material Synthesis

    Within organic electronics research and pilot-scale production, chemists employ this compound as a precursor to customized benzothiophene derivatives for organic semiconductor layers, OLED emitters, and hole-transport materials. Integration focuses on monomer purity, batch reproducibility, and downstream scalability as functionalized monomers are polymerized or coupled to tune electrical and photonic properties critical for display and sensor manufacturing.

    Industry compliance standards

    • IPC-4101B for organic substrate materials in electronics
    • RoHS Directive (2011/65/EU) for restricted substances
    • ISO 14644 for cleanroom environment production
    • Vendor-specific QC protocols (e.g., Samsung SDI, Merck KGaA)

    Typical usage ratio

    • 15–30% of total organic deposition feedstock for material development; adjusted by target film morphology, charge carrier mobility, and device architecture

    Downstream process integration

    • Undergoes functionalization or polymerization upstream of final layer deposition; controls optical gap and stacking order as electronic-grade intermediate in spin-coating, vapor, or solution processes

    Final product types

    • Benzothiophene-based monomers for OLED or OFET fabrication
    • Charge-transporting material for photovoltaic modules
    • Specialty semiconducting resins for sensor devices
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    Certification & Compliance
    More Introduction

    Methyl Benzo[B]Thiophene-2-Carboxylate:
    Precision from the Chemical Manufacturer

    Our Direct Experience with Methyl Benzo[B]Thiophene-2-Carboxylate

    Across years of producing specialized aromatic compounds, we have seen how Methyl Benzo[B]Thiophene-2-Carboxylate shapes the work of research chemists and pharmaceutical companies. From our factory floor to the packaging line, every kilogram passes through our hands and processes, giving us a front-row seat to the strengths and quirks of this molecule.

    Physical Form and Purity Matter in Real-World Use

    This compound’s reputation starts with its clean, consistent crystalline state and defined melting point, minimizing batch-to-batch headaches. Chemists in fine chemical synthesis often chase purity close to 99%, especially when their work heads to regulated pharmaceutical or agriscience labs. Our onsite teams continually calibrate instruments like HPLC and GC-MS, and we cut out samples for random checks. These steps have proven to filter out byproducts and persistent isomers, leading to low waste and fewer headaches in downstream reactions. Our ability to deliver a consistent melting point and spectral profile eliminates much of the detective work that buyers face when quality drifts between sources.

    Model and Batch Consistency: Why Structural Clarity Wins

    With every run, our engineering teams focus on the structure of the benzo[b]thiophene core. The methyl ester at the 2-carboxylate position is more than a functional label: it’s where subtle shifts in process can have an outsized impact. Minor temperature spikes or misjudged solvent ratios will change the ratio of side products, and we’ve fine-tuned our steps to minimize these scenarios. These refinements don’t only improve final purity; they give researchers freedom to skip lengthy sample pre-treatment.

    Laboratory partners come back for this compound specifically because they trust the accuracy of our characterization: clear NMR signatures, reliable melting range, and consistent element analysis. Research never runs smoothly if the initial sample underperforms or includes residual meta isomers or heavier sulfur analogues. Batch records, logged by technicians who have worked with aromatics for years, serve as a foundation for each customer’s own regulatory filings.

    Uses That Drive Our Focus

    This molecule lives in the heart of synthetic campaigns aimed at new pharmaceutical scaffolds or advanced materials. In medicinal chemistry, the benzo[b]thiophene ring presents a starting point for modification, allowing for exploration of new biological space. Researchers rely on its established core as they introduce halogenations, cross-couplings, and amide linkages, accessing generations of published structure–activity data. Our product has launched projects targeting anti-inflammatory, anticancer, and central nervous system compounds, where bench chemists demand that starting reagents do not introduce ambiguous byproducts. The methyl ester functional group brings in both stability and reactivity, giving users flexibility with ester hydrolysis or transesterification depending on their end goal.

    For the specialty chemicals sector, this compound anchors dyes and pigment intermediates. Having a reliable source of the 2-carboxylate ester reduces the failure rate in color performance tests and makes downstream customization—like sulfonation or ring substitution—more predictable. Academic labs often investigate these modifications as well, publishing their results in organic letters and catalysis journals.

    Not Just a Centrifuge Output: The Real Differences from Other Benzo[b]Thiophenes

    Every chemist knows structures matter, but experience tells that subtle structural differences can derail or accelerate a project. Many competitors in the market sell generic benzo[b]thiophene carboxylates that float between the 2- and 3- positions, or they turn up methylated at unpredictable locations. This isn’t a small detail for anybody scaling reactions: products with positional uncertainty create new, often unknown, impurities.

    We control substitution patterns using precise temperature intervals, glassware design, and reagent purity. Synthesizing the 2-carboxylate ester means avoiding decarboxylative byproducts or unwanted ring contraction, issues traced directly to variable pressure or aging catalysts. Our protocols avoid ambiguous isomerism and ensure our certificates of analysis match what actually comes out of the reactor.

    Some producers cut steps to reduce cost, risking ester hydrolysis and generating free acid that hydrolyzes further in storage—an issue uncovered through stability trials tracking retention rates over six months in real warehouse environments. What we’ve learned, and shared with partners, is that an uncontaminated methyl ester resists slow hydrolysis and delivers molecule-for-molecule reliability, even following long transport.

    Practical Considerations: Stability, Handling, and Downstream Impact

    On the production floor, batch crystallization and drying often test patience. The choice of solvent, drying pressure, and temperature walk a fine line between speed and purity. Our staff manage each drying cycle by monitoring residual solvent content, adjusting vacuum pressure and heat, and stopping long before thermal decomposition starts. These steps matter, especially since buyers increasingly run sensitive reactions downstream, sometimes in the same flask without purification. Missing a drying endpoint by fifteen minutes leaves solvents behind that react with certain bases or metal catalysts, undermining yield.

    We package each lot in sealed, inert-lined containers that prevent the same slow hydrolysis or accidental mixing that cause purity to drop during ocean transport or long-term storage. These details matter because downstream customers in pharma are sensitive to even trace differences—documentation can be delayed for months if a batch starts out unstable.

    Sustainability in Manufacturing, and How it Shapes Final Products

    Chemical manufacturers face pressure to reduce environmental impact and hazardous waste. In past years, many benzo[b]thiophene syntheses used halogenating agents or high-temperature sulfur sources that released harmful byproducts. We revisited all steps, minimizing reliance on hazardous organosulfur reagents and swapping to greener oxidants when lab trials proved they reduced waste. Wastewater from our plant undergoes staged aerobic and anaerobic treatment, cutting total chemical oxygen demand and sulfur residuals. These upgrades required years of optimization but pay off in reduced environmental risk and better relations with regulators and neighboring communities.

    Long-time customers often request sustainability data. For us, this dialogue rewards investment in higher-yield syntheses and lower-waste protocols. Chemists developing new therapeutics or crop protectants value these improvements when documenting the life-cycle of their end products, which increasingly face regulatory review on both safety and sustainability grounds. By tweaking source material ratios and piloting solvent recycling, we translate production improvements right into the user's technical documentation.

    Putting Safety First: Lessons Learned from Production

    During our early years, a minor mishap involving batch heating nearly caused a runaway reaction. This taught us that careful monitoring surpasses traditional expectation. Each run since then, we monitor every exothermic phase using real-time temperature probes and pressure shutoffs, with operators standing by to intervene at a moment's notice. This vigilance has prevented a repeat incident and, by listening to frontline workers, our engineers designed easier process shutdown features and safer ventilation.

    On the end-user side, any compound containing the benzo[b]thiophene structure needs careful handling and clear documentation, given sulfur’s tendency to form odorous or even toxic byproducts in side reactions. We provide clear storage recommendations and hazard information based not only on regulations, but also on our own internal risk reviews from years of direct handling. Better safety translates to fewer days lost to investigation or unexpected downtime.

    Market Adaptation and New Applications: What We’ve Seen Over Time

    Originally, demand centered on classic pharmaceutical research. The pattern shifted in the last decade, and we witnessed advanced materials labs request our Methyl Benzo[B]Thiophene-2-Carboxylate for organic electronics, co-monomer development, and heterocyclic dye projects. Their requests challenged us to raise documentation standards and batch traceability, especially as new fields enforce stricter audits. Again, our years of direct manufacturing experience enabled us to implement process tracking upgrades much faster than middlemen or traders could even source their next lots.

    For projects exploring new drug scaffolds, researchers now ask for not just an analytical summary, but spectra and sample batch reserves, held for years in case of future regulatory questions. Our close relationships with top synthetic laboratories gave us new insight on the value of sample retention and full documentation, which today forms a part of our product batches as standard procedure.

    Challenges Faced: Quality Control under Tight Market Pressure

    Tough years for global supply chains taught hard lessons about the stakes of quality slipping even once. Shortages of starting materials, energy cost surges, and unexpected customs delays all threatened production. Our direct ownership of both reaction and analytical equipment gave us options to recertify incoming materials, adjust process scales, or pivot quickly to verified substitute reagents. Technical staff share a deep knowledge of alternates, built from years actually running bench and pilot syntheses at scale. Outsourcing or reselling just can’t deliver the same flexibility or speed when things go off-script.

    We were able to keep delivering on time by carrying backup lots, investing in advanced chromatography and spectral analysis hardware, and cross-reacting with small-run test batches to make sure every incoming batch met our thresholds for purity and yield. These practices underline the critical difference between a manufacturer with onsite labs and a distributor two links removed from actual production.

    Why Users Should Demand the Manufacturer’s Touch

    End-users—from ambitious graduate researchers to industrial lab supervisors—routinely find value in direct lines of communication. We field technical queries that reach back into the details of batch origin, handling conditions, or unusual spectral perturbations. No middleman can supply that sort of institutional memory. In one case, a laboratory noticed slight shifts in melting point that we traced back, through batch logs, to a change in solvent system months earlier. This transparency means users don’t need to guess at the source of discrepancies or chase a supplier for incomplete records.

    By delivering every order directly from our production site, we implement specialized packing, rapid sampling, and flexible substitutions for customers with tight experimental protocols. Our quality staff routinely run cross-batch comparisons, especially on recurring orders. Over years, such attention creates a track record of reliability hard to match when product changes hands several times before the laboratory even receives it.

    Continued Improvement: What Real Feedback Yields

    The chemical industry can feel resistant to change, but face-to-face collaboration—not survey feedback—drives innovation. From direct conversations with process chemists running glass reactors or technicians prepping microbatches for scale-up, we retrieve valuable critiques: which solvent leaves less residue, which batch handles best, which affixes better to resin for purification. This process of incremental troubleshooting results in long-term improvements that cut out half steps, reduce hazardous waste, and streamline product handoff.

    Guided by dozens of such hands-on exchanges, we moved toward a more modular production workflow. If a batch calibrates slightly outside spec, instead of offloading to traders, we can efficiently reroute the process, requalify the lot, and ship validated product without delay. This policy comes directly from the needs and feedback of those who rely on timely, reliable deliveries over beautiful documentation or the lowest possible price alone.

    Tackling the Unknown: Future Applications

    The synthetic science field moves quickly. A few years ago, nobody predicted use-cases like high-conductivity polymers or sustainable pesticide intermediates. Our willingness to invest in small exploratory batches of Methyl Benzo[B]Thiophene-2-Carboxylate opened doors to these surprises. Customization requests grew, and we found ourselves collaborating closely with labs trialing unique ligands or pharmaceutical intermediates far outside the boundaries of generic benzo[b]thiophenes.

    We enable these innovations by holding enough process flexibility to pivot response: adjusting batch size, tweaking purification gradients, partnering on co-packaging for multi-step syntheses. As practical chemists, our team recognizes the importance of being ready for left-field developments and supporting pilot projects without the drag of complex purchasing bureaucracy.

    Confidence, Not Hype: What Sets Manufacturer-Grade Apart

    So many stories in the specialty chemicals market turn out to be about paperwork or pure price. Consistent results, proactive communication, and direct process accountability deliver the true hidden value, especially as more labs demand end-to-end traceability. We see customers return year after year, citing our responsiveness, our detailed batch histories, and the practical value of knowing exactly what left our facility and how it was made. The story of Methyl Benzo[B]Thiophene-2-Carboxylate in our hands is one of real-world cooperation—stretching from raw material intake to high-stakes pharmaceutical launches and advanced materials research.

    By prioritizing structure-verified product, hands-on quality control, and continuous improvement, we give each user a real edge: confidence to scale up reactions, to pursue new applications, to invest in ambitious research—all on the solid ground of tested, consistently manufactured material.