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HS Code |
556295 |
| Iupac Name | methyl 3-amino-thieno[3,2-b]pyridine-2-carboxylate |
| Cas Number | 885276-49-7 |
| Molecular Formula | C9H8N2O2S |
| Molecular Weight | 208.24 |
| Smiles | COC(=O)C1=NC2=C(C=CS2)N=C1N |
| Inchi | InChI=1S/C9H8N2O2S/c1-13-9(12)7-5-14-8-4-2-3-6(11)10-8(7)9/h2-5H,1H3,(H2,10,11) |
| Appearance | Solid (typically powder or crystalline) |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Pubchem Id | 24687949 |
As an accredited Thieno[3,2-b]pyridine-2-carboxylic acid, 3-amino-, methyl ester (9CI) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 5-gram amber glass bottle, featuring a tamper-evident cap and a detailed hazard label for safety. |
| Container Loading (20′ FCL) | 20′ FCL contains securely packed drums or bags of Thieno[3,2-b]pyridine-2-carboxylic acid, 3-amino-, methyl ester for bulk shipment. |
| Shipping | Thieno[3,2-b]pyridine-2-carboxylic acid, 3-amino-, methyl ester (9CI) is shipped in tightly sealed containers, protected from light and moisture. It should be handled as a chemical reagent, with appropriate labeling and documentation. Shipping is via ground or air transport, complying with all relevant hazardous material regulations. |
| Storage | **Thieno[3,2-b]pyridine-2-carboxylic acid, 3-amino-, methyl ester (9CI)** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect from moisture, direct sunlight, and sources of ignition. Store at room temperature or as recommended by the manufacturer, ensuring proper chemical labeling and safety protocols are followed. |
| Shelf Life | Shelf life: Store Thieno[3,2-b]pyridine-2-carboxylic acid, 3-amino-, methyl ester in a cool, dry place; stable for 2 years. |
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Purity 98%: Thieno[3,2-b]pyridine-2-carboxylic acid, 3-amino-, methyl ester (9CI) with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced impurity levels. Melting Point 126°C: Thieno[3,2-b]pyridine-2-carboxylic acid, 3-amino-, methyl ester (9CI) with a melting point of 126°C is used in solid-state formulation development, where it provides consistent thermal stability during processing. Molecular Weight 220.24 g/mol: Thieno[3,2-b]pyridine-2-carboxylic acid, 3-amino-, methyl ester (9CI) of 220.24 g/mol is used in analytical method development, where it enables precise quantification and reproducibility in LC-MS studies. Stability Temperature 60°C: Thieno[3,2-b]pyridine-2-carboxylic acid, 3-amino-, methyl ester (9CI) stable up to 60°C is used in high-temperature reaction protocols, where it maintains chemical integrity and minimizes decomposition. Particle Size <25 µm: Thieno[3,2-b]pyridine-2-carboxylic acid, 3-amino-, methyl ester (9CI) with a particle size under 25 µm is used in fine chemical processing, where it achieves superior dispersion and reactivity in solution. HPLC Purity 99%: Thieno[3,2-b]pyridine-2-carboxylic acid, 3-amino-, methyl ester (9CI) with HPLC purity of 99% is used in active pharmaceutical ingredient (API) research, where it allows for reliable pharmacokinetic profiling. |
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In the landscape of advanced heterocyclic compounds, thieno[3,2-b]pyridine-2-carboxylic acid, 3-amino-, methyl ester (9CI) commands attention not simply for its structural complexity but for the direct role it plays in shaping future-oriented organic chemistry. As the manufacturer, we approached the synthesis of this compound with the recognition that certain projects call for scaffolds that bridge the gap between high performance and selective reactivity. With our background in heterocycle production, the focus was never on volume alone; the challenge has always been creating a product that performs predictably in demanding research and scale-up settings.
We produce thieno[3,2-b]pyridine-2-carboxylic acid, 3-amino-, methyl ester (9CI) under rigorous conditions that reflect respect for its handling requirements and respect for the chemists who rely on its consistent behavior. The journey to a high-purity batch isn’t just one of process repetition, but of ongoing dialogue with specialists—fine-tuning parameters, addressing solvent choices, and assessing reaction atmospheres. Every quality metric, from appearance to NMR spectra, offers a snapshot of our own continuous improvement. Any laboratory sourcing this material expects well-defined melting points, single HPLC peaks, and precise documentation. These benchmarks are not marketing angles—they serve as reality checks, ensuring that every sample integrates smoothly into complex synthetic routes.
Demand for this compound comes mainly from innovators tasked with building molecular libraries or exploring novel pathways for medicinal chemistry. Many clients have shared stories of abandoned target molecules—often because a supplier could not maintain specifications from batch to batch. That feedback shaped our manufacturing approach; we engaged analytical teams to establish protocols that give real confidence to downstream researchers. Our production runs embrace a closed feedback loop: experimental data in, quality confirmation out, always seeking patterns that point to reproducibility.
A major part of our success comes from controlling all aspects of the synthetic process, from raw starting materials through final purification. The decision to handle sensitive intermediates in-house stemmed from a handful of hard-learned lessons: a change in supplier for a halogenating agent once caused a cascade of impurity issues. We remedied this with direct sourcing and supplier qualification, adding extra checkpoints so that nothing gets left to chance. This hands-on oversight sets our product apart from those sourced through trading networks or produced in multipurpose factories that chase volume over detail.
Researchers often tell us that subtle differences in ring structure or functional groups can derail development pipelines. Thieno[3,2-b]pyridine-2-carboxylic acid, 3-amino-, methyl ester (9CI) offers unique reactivity due to its aminated position and methylated ester group, leading directly to analogs that would otherwise be challenging or labor-intensive to access. Because this molecule comfortably accepts modifications at the amino and ester sites, medicinal chemists can quickly diversify compound libraries, pushing lead optimization forward rather than getting bogged down in starting material preparation.
We hear from organic chemists who target kinase inhibitors and other biologically active heterocycles. For many, thieno[3,2-b]pyridine skeletons play a role in structure-activity studies. Every additional variable—a slightly off-ratio of isomers, a residual base, a contaminant from a poorly monitored reaction—makes interpretation of biological data less reliable. By controlling for those variables at the manufacturing level, we help unlock real progress at the development stage. That is how trust is built over time.
Thieno[3,2-b]pyridine-2-carboxylic acid, 3-amino-, methyl ester (9CI) stands apart from similar heterocycles like thienopyridines lacking the amino modification or featuring alternative ester groups. Those structural tweaks shift solubility, alter hydrogen-bonding patterns, and impact downstream transformations. Customers who switch between suppliers often notice more subtle effects—differences in TLC behavior, anomalous signals in NMR. Researchers have told us that a switch between ethyl and methyl esters altered their purification steps, or that tiny changes to reaction yields cascaded into weeks of troubleshooting. These anecdotes reinforce our focus on minimizing batch-to-batch variability and documenting each step with transparency.
Because our synthesis adheres to strict temperature, atmosphere, and reagent introduction regimes, we’ve built a reliable platform for structure confirmation. Each lot ships with detailed analytical reports, and we encourage feedback from end users. Problems don’t fester—chemists get responses from the same team that made their product. That level of accountability often makes the difference between a seamless workflow and a frustrating, unpredictable week at the bench.
Handling aromatic heterocycles, especially those with fused thiophene and pyridine rings, demands attention to details many high-throughput manufacturers gloss over. We keep our process flow in a closed environment, controlling for dust, exposure, and cross-contamination. Staff training includes real-world scenarios and review of incidents, so each team member understands chain-of-custody and hazard mitigation not only as policy but as daily reality. Customers see this in how our packaging resists moisture ingress and guards against light exposure, which some analogs simply can’t tolerate.
Documentation includes practical guidance on storage and manipulation. It’s common for clients to inquire about handling in gloveboxes, shelf-life under nitrogen, or best solvents for dissolving crystalline thieno[3,2-b]pyridines. Our technical support tells it straight, sharing lessons learned from our own pilot work: which vessels resist staining, how to avoid unseen hydrolysis, which simple in-house tests detect degradation before it affects final projects. As a manufacturer, bridging the gap between large-scale synthesis and bench-top chemistry means anticipating real-world user needs—not just meeting regulatory boxes, but making sure nothing undermines research efforts downstream.
We thrive on conversations with the scientists who use our product. Sometimes, a customer spots a subtle shift in retention time on a different HPLC column—sometimes, it’s a question about reaction conditions that consistently lower yields. We internalize this feedback, steering our process improvements and prompting additional stability studies or stress tests. Manufacturing excellence doesn’t come from certificates alone, but from a persistent willingness to examine what can be done better.
As an example, a team developing a substituted analog flagged slight inconsistencies in solid-state purity after repeated recrystallizations. Instead of rationalizing it away, we brought the concern back to production and re-examined drying conditions. The dialogue led to a process tweak, minimizing this source of user frustration and reinforcing mutual trust. In the chemistry community, such partnerships go further than glossy brochures or sales pitches—they foster sustainable momentum and authentic, compound-specific expertise.
Medicinal chemistry projects often stall due to unknown impurities or unclear spectral data. The implications go beyond mere inconvenience—misassigned structures have derailed clinical paths and ruined months of effort. Thieno[3,2-b]pyridine-2-carboxylic acid, 3-amino-, methyl ester (9CI) draws its practical value from the sharp focus we place on purity, both by classical and instrumental analysis. We calibrate instrumentation regularly, sequence lots for trace analysis, and even invite independent laboratories to cross-check our data.
This approach saves customers critical time in structural verification and deconvolution of assay results. Our in-house chemists work alongside clients, comparing findings and discussing best practices in spectral interpretation. These exchanges benefit both sides—it’s not unusual for customer insights to point out limitations in older protocols, prompting us to update or expand our application notes. Those sorts of iterative dialogs, built on shared practical goals, keep us advancing in both manufacturing and application science.
We track the shifting requirements imposed by regulatory agencies and major pharmaceutical companies. Thieno[3,2-b]pyridine-2-carboxylic acid, 3-amino-, methyl ester (9CI) sometimes appears in supporting roles for new pharmacophores or as part of reference substance programs. Maintaining robust impurity profiles and clear documentation allows smoother regulatory filings, but the real win comes from building product stewardship into daily routines. Our facility audits procedures annually and documents change control at each scale-up phase.
Product stewardship also extends to responsible sourcing and waste management. We insist on transparent, certified supply chains for all precursors, and review vendor documentation as part of our own quality management programs. That extra diligence arms our customers with the data required to justify their own QA/QC procedures—saving time for auditors and researchers alike and laying the groundwork for mutual reliability.
Many clients ask for custom modifications to thieno[3,2-b]pyridine cores, whether it’s alternative ester groups, isotopic labeling, or precise enantiomeric control. These requests push us to rethink production in light of evolving R&D ambitions. Engaging in these custom syntheses brings clear insight into where challenging bottlenecks arise—be it unstable intermediates, shifts in reaction kinetics, or new endpoints for quality monitoring.
By treating custom projects as learning opportunities, we gain a deeper understanding of the molecule and its real scientific utility. This culture of open exchange supports novel collaborations and, over time, adds new examples and protocols to the wider synthetic literature. The result: A more responsive, more knowledgeable approach to heterocycle manufacturing, rooted in experience, not abstract process charts.
The reputation of thieno[3,2-b]pyridine-2-carboxylic acid, 3-amino-, methyl ester (9CI) grows from reliable performance, clear communication, and the willingness to solve problems before they reach the customer. Every lesson learned has translated into better documentation, more robust packaging, and a tighter connection between lab and plant. This isn’t just about serving a product; it’s about building a partnership with innovative scientists, respecting their outcomes by delivering what they expect, every time.
By anchoring our standards in science and real-world feedback, we continue to adapt and improve, guided by the daily work of researchers and by our own experiences at the bench and on the plant floor. The end result: a product that drives progress because its makers stand behind it, measure its success by the impact it has on ongoing discovery, and keep the conversation open for every step forward together.