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2-Amino-4,5,6,7-Tetrahydro-Benzo[B]Thiophene-3-Carboxylic Acid Methyl Ester

    • Product Name 2-Amino-4,5,6,7-Tetrahydro-Benzo[B]Thiophene-3-Carboxylic Acid Methyl Ester
    • Alias Methyl 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate
    • Einecs 681-984-8
    • 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

    426322

    Iupac Name Methyl 2-amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate
    Molecular Formula C10H13NO2S
    Molecular Weight 211.28 g/mol
    Cas Number 120672-73-9
    Appearance White to off-white solid
    Solubility Soluble in common organic solvents (e.g., DMSO, methanol)
    Smiles COC(=O)C1=C(N)SC2CCCC2C1
    Storage Conditions Store in a cool, dry place, keep tightly closed
    Pubchem Cid 10128301
    Synonyms Methyl 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate

    As an accredited 2-Amino-4,5,6,7-Tetrahydro-Benzo[B]Thiophene-3-Carboxylic Acid Methyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, opaque plastic bottle with secure screw cap, labeled "2-Amino-4,5,6,7-Tetrahydro-Benzo[B]Thiophene-3-Carboxylic Acid Methyl Ester, 25g".
    Shipping This chemical ships in a secure, sealed container to ensure stability and prevent contamination. It is packaged according to safety and regulatory guidelines for hazardous materials. Shipping includes clear labelling, appropriate cushioning, and temperature control if required. A safety data sheet accompanies each shipment for handling and emergency reference.
    Storage Store 2-Amino-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxylic acid methyl ester in a tightly sealed container, protected from moisture and direct sunlight. Keep it in a cool, dry, and well-ventilated area, ideally at 2–8°C (refrigerator) unless otherwise specified by the manufacturer. Avoid exposure to strong oxidizing agents and incompatible materials. Ensure proper labeling and access is limited to qualified personnel.
    Application of 2-Amino-4,5,6,7-Tetrahydro-Benzo[B]Thiophene-3-Carboxylic Acid Methyl Ester

    Applications of 2-Amino-4,5,6,7-Tetrahydro-Benzo[B]Thiophene-3-Carboxylic Acid Methyl Ester in Industrial Manufacturing

    As an established manufacturer, we provide 2-Amino-4,5,6,7-Tetrahydro-Benzo[B]Thiophene-3-Carboxylic Acid Methyl Ester to a focused base of industrial customers. The applications below illustrate the actual integration of our material in several downstream processing fields where its chemical structure and properties address critical process requirements.

    1. Advanced Pharmaceutical Intermediate Synthesis

    Our material frequently serves as an advanced intermediate for synthesizing complex heterocyclic active pharmaceutical compounds, especially in small-molecule APIs development. Pharmaceutical manufacturers employ the ester group for direct coupling or hydrolysis to access free acid intermediates. It enters multi-step synthesis pathways, benefitting from high reactivity under mild conditions. This integration minimizes by-product formation and offers firm control over product yield and purity. The downstream pathway adopts inline reaction monitoring to assure batch reproducibility and regulatory compliance.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • European Pharmacopoeia (Ph. Eur.) standards for intermediates
    • US FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • Chinese Pharmacopoeia compliance for raw material controls

    Typical usage ratio

    • 5% to 20% molar ratio as a core building block in multi-step flows; actual loading adjusted based on route design and batch scale

    Downstream process integration

    • Charged at Stage 2 or higher in API synthesis; typically enters after base structure assembly to introduce thiophene moiety
    • Utilized in amidation, Suzuki coupling, or ester hydrolysis stages under controlled temperature and pH
    • Reacts under nitrogen atmosphere to suppress oxidative degradation
    • Subjected to purification (such as flash column or crystallization) before entering final API coupling steps

    Final product types

    • Active pharmaceutical ingredients (APIs) for neuroprotective drugs
    • Anti-inflammatory drug intermediates
    • Novel central nervous system (CNS) drug candidates
    • Reference standards for analytical and regulatory submissions

    2. Development of Agrochemical Actives

    Agrochemical formulators employ this compound as a key intermediate in producing selective fungicide and insecticide molecules. The compound’s heterocyclic core structure contributes to high binding affinity for target enzymes in pests and plant pathogens. Process control includes overseeing hydrolysis and substitution reactions to install crop-specific functional groups. Material purity and residual solvent content must meet strict local and international criteria due to traceability requirements and safety assessments.

    Industry compliance standards

    • FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act, USA)
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • ISO 17025 laboratory accreditation for QC testing
    • China GB/T 1604-2016 for agrochemical intermediates

    Typical usage ratio

    • 8% to 14% w/w depending on the final molecule’s synthetic complexity and intended application spectrum

    Downstream process integration

    • Fed into intermediate coupling step for new triazole or strobilurin scaffold synthesis
    • Undergoes substitution reactions (nucleophilic/electrophilic) to attach custom side chains or halogen groups
    • Subject to final step purification and residual solvent analysis before formulation
    • Integrates into pilot and large-scale plant runs with real-time process analytical technology (PAT)

    Final product types

    • Systemic fungicide actives for cereal and fruit crops
    • Insecticidal intermediates for rice farming
    • Formulation bases for combined pest management agents
    • Benchmark samples for pesticide residue labs

    3. Material for Specialty Dye Synthesis

    Manufacturers in the fine chemical sector utilize this raw material for the synthesis of high-performance dyes and colorants. Its unique thiophene core enables the introduction of extended π-conjugation through further functionalization, which imparts enhanced lightfastness and thermal stability in the final pigment structures. Strict batch consistency is necessary to avoid hue variation for industrial textiles or plastics. Downstream processes often operate under closed-loop solvent recovery to meet environmental and product safety guidelines.

    Industry compliance standards

    • REACH Regulation (EU) 1907/2006 for chemical safety
    • OEKO-TEX Standard 100 for dye contaminants
    • ISO 9001:2015 QMS for color and pigment production
    • EN 71-3 for pigment use in children’s toys

    Typical usage ratio

    • 2% to 8% by mol as the primary nucleophilic aromatic module; varying with color depth and chromophore strength desired

    Downstream process integration

    • Introduced in initial ring construction or core extension phases of dye molecule assembly
    • Undergoes electrophilic aromatic substitution or cross-coupling reactions
    • Subjected to QA for batch-to-batch color consistency
    • Feeds into final salt formation or dispersant blending before product dispatch

    Final product types

    • Technical textile dyes for automotive upholstery
    • Thermal transfer pigments in specialty printing inks
    • Plastic colorants for high-temperature applications
    • Conductive polymeric pigments for electronics

    4. Intermediate in Heterocyclic Building Block Supply

    Research and custom synthesis firms source this methyl ester as a modular building block for constructing various fused bicyclic and tricyclic heterocycles. Its structure allows for selective amination, oxidation, or ester cleavage, supporting the rapid assembly of diverse libraries for pharmaceutical or material science uses. The integration process requires precise control over reaction stoichiometry, temperature, and impurity profile to meet client screening library requirements. Post-reaction, extensive LC-MS and NMR analysis ensures delivered fractions meet narrow specification bands.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for raw material handling
    • GMP-like documentation for chemical research supplies
    • Sigma-Aldrich Aldrich Sure/Select standards as a secondary reference
    • Internal client purity and structural standards for library compounds (often >98%)

    Typical usage ratio

    • 1% to 10% w/w, adjusted according to the complexity of the targeted heterocycle; higher ratios for multi-component reactions

    Downstream process integration

    • Reacted in sealed reactors during stepwise amination or cyclization
    • Feeds both solution-phase and solid-phase synthesis platforms
    • Handled in anhydrous or oxygen-controlled settings to minimize side-product formation
    • Undergoes immediate fractionation or chromatography within the same day to maintain integrity

    Final product types

    • Diversity-oriented synthesis (DOS) compound libraries for pharmaceutical screening
    • Modified heterocycles as material science standard references
    • Lead compound scaffolds for medicinal chemistry programs
    • Custom research samples for university and industrial R&D
    Free Quote

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    Certification & Compliance
    More Introduction

    2-Amino-4,5,6,7-Tetrahydro-Benzo[B]Thiophene-3-Carboxylic Acid Methyl Ester: Trusted Quality from the Manufacturer’s Floor

    Shaped by Practical Manufacturing Experience

    Every batch of 2-Amino-4,5,6,7-Tetrahydro-benzo[b]thiophene-3-carboxylic acid methyl ester that leaves our facility reflects the daily reality of working with sulfur-containing heterocycles and the demands placed on intermediates in modern chemical development. This compound, though its name can look intimidating at first glance, earns its spot on our line due to its steady performance in synthesis scenarios where precision and stability matter. From process to practice, it stands as a familiar backbone for researchers working on pharmaceuticals, fine chemicals, or specialty materials that lean on the unique blend of aromaticity and flexibility present in the benzo[b]thiophene system.

    Many years in chemical synthesis push a team past the point of seeing a product as just a formula or code. Our crew learns the quirks of each molecule, the subtle cues from color and texture, and the way tiny shifts in process conditions ripple through a production run. With this API intermediate, the methyl ester modification improves certain reactivity features and solubility traits compared to its free acid sibling. Staff recognize when its crystalline form comes out right and know the satisfaction of seeing a clean NMR spectrum after a carefully controlled batch. Our protocols around this methyl ester grew through repeated runs and real-world feedback from our own laboratory and pilot plant projects.

    Why This Methyl Ester Matters Beyond the Lab Bench

    Sulfur-containing intermediates rarely linger on the shelf. This compound draws considerable attention from medicinal chemists searching for a reliable building block that tolerates a broad range of reaction conditions. We see its core framework woven into experimental CNS agents and, at times, into agrochemical leads that owe their activity to the unique profile of this fused ring. The methyl ester group—no mere afterthought—offers just enough mobility during coupling reactions. Friends in synthetic teams mention how the compound’s clean reactivity helps circumvent side reaction issues they run into when using less substituted analogues.

    From our side, physically handling the solid form day-in and day-out, one learns how small variations in particle size or moisture content change the way a charge flows into a reactor. These aren’t academic concerns. Consistency at the 100 kg batch level separates suppliers meeting scale-up timelines from those causing monthly headaches. We’ve put a lot of attention into controlling drying curves, optimizing filtration steps, and maintaining batch-to-batch reproducibility. Every improvement traces back directly to our technicians’ feedback and analytical lab’s close monitoring. There’s a certain pride in shipping drums that look identical whether they’re bound for a start-up lab or a multinational pilot program.

    The Value Built Into Our Product Experience

    Working as a direct manufacturer means living with every tweak to process optimization—facing practical consequences and real costs when a run doesn’t meet expectations. We set our specifications around both analytical purity and practical usability, based on the granular reality of our operation. This establishes a reference point for our production team: GC-MS and HPLC backing up hands-on tests for flow, color, and melting point. By the time our methyl ester variant leaves the warehouse, it’s passed through several pairs of experienced eyes and hands, not just automated quality-control software.

    Customers remark on the transparency we maintain about each product’s journey—where it originates in our raw materials, how it’s monitored, cleaned, and packaged. That traceable thread from starting material to finished drum gives researchers downstream more confidence as they pursue new actives or seek regulatory approvals. Our shared commitment to documentation never drifts into bureaucracy; rather, it keeps us grounded in the practical truth of daily operations. Audit teams visiting our site see our work in action, not just in records.

    What Sets This Compound Apart from Similar Intermediates

    Plenty of chemical suppliers offer aromatic methyl esters or thiophene-building blocks, but many lack the production depth or specialized know-how we have accumulated with benzo[b]thiophene derivatives. In practice, many competitors deliver products with acceptable nominal purities, but close inspection reveals unaddressed trace impurities or inconsistent appearance from one drum to the next. These small oversights magnify downstream, often forcing reactive purification steps and introducing scheduling uncertainty.

    On our end, our experience turning out production runs for both research and commercial-scale customers means we continually close gaps in process reliability. Our staff’s focus on high-throughput purification and chromatographic evaluation cuts down on risk. Direct communication with end-users lets us immediately troubleshoot any observed solubility, stability, or compatibility hiccups. If tendering to pharmaceutical partners, we anticipate questions about both elemental impurities and residual solvents—issues best addressed face-to-face between chemists, not through secondary resellers.

    From a more hands-on perspective, colleagues in R&D appreciate the convenience of the methyl ester group in this context. They comment on its cooperative profile in alkylation, acylation, and amide-coupling reactions compared to bulkier or more labile ester derivatives. Achieving high yields and clean transitions into subsequent synthetic steps becomes routine rather than exceptional—an outcome shaped by careful selection of starting reagents and a few critical steps often honed through after-hours experimentation.

    Behind Every Lot: Leaning on Experience Over Theory

    Unlike outsourcers or catalog middlemen, we process each order from raw material receipt to final shipment—a long, sometimes unpredictable journey. Building trust batch after batch starts with the hands mixing the reactants and ends with the logistics team ensuring a reliably packed and labeled container lands at its destination in good condition. Over the years, our operators learned to recognize lot-to-lot nuances. Minor color shifts might mean only a slight adjustment in drying time, but we know how to catch these small changes before they influence a product’s performance in the next synthetic step.

    Every customer inquiry becomes an opportunity for us to share insights from past problem-solving runs. If a downstream reaction shows an unexpected byproduct or a solubility twist, we’re ready to revisit preparative records and sample out representative lots to replicate their scenario and dig into root causes. Our continual tracking—NMR, FTIR, moisture analysis, and specialist impurity screening—evolves with both regulatory landscapes and the creative ambitions of academic and industrial chemists.

    Standing Up for Transparency in Chemical Manufacturing

    Working inside a manufacturing facility means seeing the entire universe of pressures facing modern chemistry. Environmental compliance and process safety are never background concerns; they help guide all routine choices. Our methyl ester product draws on decades of environmental safety protocol design. By integrating emission mitigation steps, solvent recycling, and containment engineering, we keep occupational exposure low and waste streams manageable. We believe meeting these standards benefits every party downstream and sustains the long-term use of compounds like this across the industry.

    Production runs translate regulatory intent into physical outcomes. Our batch monitoring doesn’t just tick regulatory boxes; it tells us where wastage or process drift might sneak in. Attention to solvent purity, validated cleaning, and complete documentation form the backbone of our daily work. Each improvement—an extra minute in a drying cycle, a finer grind, a shift to a lower-residue solvent—emerges from dialogue between process chemists and operators. This real-world feedback loop creates practical improvements that persist across product lines and generations of plant staff.

    Practical Solutions to Manufacturing Challenges

    The reality of producing advanced intermediates means facing, and adapting to, ever-changing raw material availability and evolving synthetic priorities. Our sourcing group vets suppliers not just for price, but for consistency, traceability, and backup planning. The same logic applies to energy management. Whether power disruptions threaten a batch or a key plant utility nears downtime, our maintenance crew steps in before anomalies become lost product. This diligence reduces waste and keeps promised delivery dates meaningful.

    Technicians on the floor confront unpredictable events—a pump hitting low pressure, a filtration step slowing down in humid weather, or a drum closing that needs resealing after a snowstorm supply run. Each instance brings out lessons that shape future protocols. For example, summer high temperatures near crystallization zones prompted ventilation and scheduling adjustments; winter freezes led to modified storage practices. Over time, these “minor” adaptations stack up, yielding a consistent final product no laboratory-scale synthesis or distributor repack offers.

    Looking Forward: Meeting Tomorrow’s Industry Needs

    Throughout our history, we watched needs shift from high-volume bulk commodities to targeted, high-purity niche intermediates. Now, customers often demand adaptability—revised specifications, novel grades, or integrated analytical services. Our team approaches each new request with the same on-the-ground mentality that guides our core methyl ester production. Direct lines of communication with researchers and development chemists make a real difference during scale-up or regulatory reviews. They want answers born from direct experience, not generic corporate policies.

    In response, our technical team ramped up both our analytical depth and responsiveness. Expanded capabilities in LC-MS, long-term stability monitoring, and impurity tracing allow us to anticipate rather than simply react to changes in customer demands. We maintain close ties with academic groups advancing benzo[b]thiophene chemistry and partner with industrial consortia tracking regulatory and toxicological changes. Our commitment roots itself not just in the compound’s profile, but in a systems-level awareness of how each molecular batch moves through customer hands toward its final service—be that a medication, crop science agent, or specialty additive.

    Why Manufacturers Matter More Than Ever

    Direct chemical manufacturers stand at an intersection between traditional craft and modern science. We think this compound’s journey best illustrates this unique role. No catalog copy or distributor’s promise substitutes for the everyday business of monitoring, adapting, and improving batch processes. By keeping our focus both on the shop floor and in customer labs, we build something more enduring than a single intermediate—a reputation for consistency, trust, and accountability achieved only through repeated, hands-on engagement with challenging chemistry.

    Every shipment of 2-Amino-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxylic acid methyl ester from our site reflects proven practice and the effort of a team committed to continuous learning. We view each order as both a technical and professional responsibility. The long-term partnerships that emerge from this shared commitment keep us motivated to refine, innovate, and deliver a product that chemists expect, industry needs, and global progress relies on.