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HS Code |
358597 |
| Compound Name | 7-Chloro-2-iodothieno[3,2-b]pyridine |
| Molecular Formula | C7H3ClINS |
| Molecular Weight | 295.53 g/mol |
| Cas Number | 1049127-77-2 |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Solubility | Soluble in common organic solvents (e.g., DMSO, DMF) |
| Smiles | C1=CC2=C(C(=N1)I)SC=C2Cl |
| Inchi | InChI=1S/C7H3ClIN2S/c8-4-1-2-6-5(9)10-3-7(6)11-4/h1-3H |
| Storage Conditions | Store at 2-8°C, protect from light and moisture |
| Synonyms | 7-Chloro-2-iodo-thieno[3,2-b]pyridine |
As an accredited 7-Chloro-2-iodothieno[3,2-b]pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Supplied in a 1g amber glass vial, sealed with a screw cap. Clearly labeled with chemical name, CAS number, and hazard warnings. |
| Container Loading (20′ FCL) | 20′ FCL container typically loads about 8-10 MT of 7-Chloro-2-iodothieno[3,2-b]pyridine, securely packaged in drums or bags. |
| Shipping | 7-Chloro-2-iodothieno[3,2-b]pyridine is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is handled as a hazardous material and transported according to relevant chemical safety regulations, typically via ground or air freight with appropriate labeling and documentation to ensure safe delivery. |
| Storage | 7-Chloro-2-iodothieno[3,2-b]pyridine should be stored in a tightly closed container, kept in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Protect from moisture and heat. Handle under inert atmosphere if required, and ensure proper labeling and secure storage to prevent accidental release or contamination. |
| Shelf Life | 7-Chloro-2-iodothieno[3,2-b]pyridine is stable for at least 2 years when stored cool, dry, and protected from light. |
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Purity 98%: 7-Chloro-2-iodothieno[3,2-b]pyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction selectivity and product yield. Melting point 162°C: 7-Chloro-2-iodothieno[3,2-b]pyridine with a melting point of 162°C is used in medicinal chemistry research, where it supports stable solid-state compound formation. Molecular weight 314.55 g/mol: 7-Chloro-2-iodothieno[3,2-b]pyridine with a molecular weight of 314.55 g/mol is used in heterocyclic compound libraries, where it facilitates accurate structure-activity relationship studies. Stability temperature up to 80°C: 7-Chloro-2-iodothieno[3,2-b]pyridine with stability up to 80°C is used in organic synthesis processes, where it maintains structural integrity during temperature-dependent reactions. Particle size <10 µm: 7-Chloro-2-iodothieno[3,2-b]pyridine with particle size less than 10 µm is used in process formulation development, where it enhances dispersion and reaction efficiency. |
Competitive 7-Chloro-2-iodothieno[3,2-b]pyridine prices that fit your budget—flexible terms and customized quotes for every order.
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Every day on our production floor, the commitment to precision starts with raw materials we trust and ends with products built for practical use in modern chemical research. 7-Chloro-2-iodothieno[3,2-b]pyridine stands out in our lineup as a carefully engineered heterocyclic compound. Over years of direct manufacturing, our familiarity with its characteristics has shaped the way we handle synthesis, testing, and packaging for both scale and consistency.
The structure of 7-Chloro-2-iodothieno[3,2-b]pyridine brings together two key halogens—chlorine and iodine—on a fused thienopyridine ring system. Chemists working in drug discovery and advanced material fields recognize the distinct value that dual halogenation offers. By placing a chlorine at position 7 and an iodine at position 2, chemists have an effective synthetic handle. Common requests for this compound are for material in the 97% or higher purity range, because both pharmaceutical intermediates and specialty chemical innovators notice the difference when impurities creep above 2%: yields drop, side reactions occur, reproducibility falters. Since our plant deals with kilogram to multi-ton batches, we’ve seen how subtle shifts in reaction temperature, solvent purity, or halide sources can tip yield or color. Each lot receives HPLC, NMR, and mass spectrometry checks, because one overlooked contaminant often wastes weeks of customer time.
Chemists approaching scale-up or structure-activity relationship studies look for heteroaryls that offer multiple derivatization points. 7-Chloro-2-iodothieno[3,2-b]pyridine fills this gap at the intersection of cost, versatility, and reactivity. Medicinal chemists, in particular, select it for cross-coupling strategies—Suzuki, Sonogashira, and Buchwald-Hartwig routes—because the iodine at C2 acts as a highly reactive leaving group. The 7-chloro drives regioselectivity while adding electron-withdrawing character, subtly altering reactivity in ways not achieved with non-halogenated or mono-halogenated analogs. From our experience supplying both academic and industrial labs, 7-chloro-2-iodo derivatives form the core of libraries targeting kinase inhibitors, anti-infectives, and select organic semiconductors.
Some clients investigate direct arylation or C-H activation methods on this skeleton. The ability to selectively functionalize the iodine or the ring positions without excessive side products comes as a result of tight process control and fresh stock: old or hygroscopic material always gives headaches at the bench scale. Over the past year, we’ve responded to feedback about sensitivity to moisture and light by installing additional light-impermeable packaging and using desiccant systems in all outgoing shipments. This direct line of feedback from the bench to our blending and filling teams aligns with our understanding that wasted time costs more than any slight savings in raw production.
Having handled dozens of thienopyridine derivatives, we observe significant performance contrasts between 7-Chloro-2-iodothieno[3,2-b]pyridine and its relatives. For example, the mono-chloro version—lacking the iodine—simply won’t deliver the rapid oxidative addition chemists need in many coupling strategies. Iodinated-only thienopyridines have a tendency for off-target byproducts in certain palladium-catalyzed couplings due to increased soft character on the ring, sometimes resulting in reductions or ligand exchange issues. The addition of chlorine shifts the electron density, which our internal studies have linked to both higher selectivity and improved crystalline stability, especially useful for those isolating intermediates by precipitation or filtration. While these are details not always reported in literature, our technical support staff hears from frustrated researchers who compared products from various suppliers, only to find unacceptably slow or capricious reactivity in their set-ups.
Another distinction arises in packaging and shelf-life. Based on our stability studies under both real and accelerated conditions, the chlorine-iodo combination tolerates moderate heat and humidity better than more heavily iodinated analogs, which tend to yellow or decompose if left uncapped or in sunlight. Firms working at remote sites or in limited-infrastructure labs require materials that travel well and arrive intact. Consequently, we moved away from semi-permeable containers toward heavy-duty, re-sealable options with clear desiccant indicators. These changes came directly after feedback from European and Southeast Asian clients who lost several grams to ambient water uptake or light damage, proof that responses to such issues demand an active listening stance from producers.
From our end, the production of 7-Chloro-2-iodothieno[3,2-b]pyridine always starts with consistent sourcing of thienopyridine precursors. Price volatility in the halogen and solvent markets continues to threaten batch reproducibility and customer pricing. In the past two years, we’ve dealt with disruptions in the supply of specialty iodine compounds. To protect our users against sudden shortages or variance in performance, we maintain in-house reserves and multi-source agreements, so even if a global shortage surfaces, our output stays reliable. Our synthetic process relies on carefully optimized halogenation steps, followed by rigorous purification. Teams in our analytics department track impurity profiles by the lot so research customers get actionable, batch-specific certificates tied to exact impurity thresholds.
We’ve also seen the difference that genuine manufacturer support makes in customer projects. Direct contact with production chemists—not sales representatives—lets us answer questions about solubility in uncommon solvents, custom particle size requests, and help users avoid failure-prone paths. This means less reliance on speculation and more actionable results for our clients running real experiments, not just hypothetical ones.
The population of researchers turning to halogenated thienopyridines has clearly grown in the past decade. With new kinase targets and optoelectronic applications in development, demand stems from the flexibility of this scaffold’s substitution pattern. Having delivered this product to both grand-scale pharmaceutical plants and tiny biotech start-ups, we see common patterns in usage and troubleshooting. Success often depends as much on the lot’s physical handling as its molecular quality. Grasping the nature of this sensitivity comes only after repeated direct contact with the material—from seeing how quickly certain batches 'cake' in open air, to observing subtle color changes from storage. We encourage users to communicate practical difficulties, so improvements on future lots reflect real-world lab expectations.
In catalysis applications, our process chemists have tailored drying and packaging steps so that residual water or oxygen interference is consistently sub-ppm. Those running sensitive cross-coupling reactions or scaling up to multistep synthesis directly benefit from this extra care, reporting fewer failed runs and cleaner downstream purifications.
Producing 7-Chloro-2-iodothieno[3,2-b]pyridine does not always go according to plan. Years ago, we underestimated the stability risk posed by iodine-containing materials stored at high room temperatures. Complaints about off-color or sluggish product prompted our technical teams to reevaluate both antioxidant use and UV stabilization. By switching packaging types and reinforcing storage advice for customers, we now see higher retention of expected appearance and fewer returns. Technical feedback influences our scheduling: we hold off on scaling up unless analytics show deviation is below the tightest historical limits. Problems that creep in at this stage—trace metals, halogen overshoot, solvent residues—rarely escape experienced eyes, so our staff remains vigilant at every QC checkpoint.
Another area of learning: not every use case fits best practice. Some clients contacted us after running the product in unconventional solvents, finding unexpected insolubility or degradation. In such cases, direct advice from a synthetic chemist who has handled the same lot typically resolves confusion faster than a standard FAQ. Sustained, detail-focused communication between our plant and end users consistently results in fewer project delays for clients and lower waste in our own facility.
End users benefit most by sourcing directly from those who actually formulate and test each batch. In our operation, technical feedback flows from user bench to production and back, so error corrections and process improvements emerge rapidly. Open dialogue often leads to customizations not available from stock resellers: unusual particle sizes, bulk packaging for automated feeders, modified purity grades for regulatory submissions. Since our quality management systems link every outgoing lot to raw supplier batches, deviations in final product can be traced, corrected, and prevented in real time. That accountability can’t be matched by trading intermediaries who merely move sealed drums without first-hand process control.
Clients increasingly request support documentation: NMR spectra, purity certificates, impurity maps, and MSDS documents tailored to specific national requirements. Providing these up front, tied to unique batch numbers, reduces time lost chasing discrepancies later. We maintain archives of all analytical results and protocol changes so repeat orders reflect the cumulative lessons from previous runs. This open framework of evidence and transparency distinguishes manufacturers invested in quality from bulk re-packagers driven only by volume.
We approach each year of production seeking tangible ways to reduce batch variability and environmental impact. Over the last year, our green chemistry team targeted halogen waste in the synthetic process, converting a previously disposable stream into a recyclable byproduct. Not every experiment yields instant savings, but ongoing process optimization based on lab-scale results often leads to facility-wide efficiency gains. Direct engagement with frontline researchers allows us to test and refine handling protocols: lighter, break-resistant containers; improved tamper-evident sealing; and partially automated weighing systems for smaller fills.
We see future demand drivers coming from both established markets and new discovery fields—next-generation electronics, precision agricultural chemicals, and advanced imaging agents. In each of these, researchers demand provenance and consistency from their starting materials. As a vertically integrated producer, we control every variable from precursor sourcing through final packaging, which lets us provide information and service above generic commodity suppliers. Every improvement we make grows out of real-world laboratory needs, not market speculation.
As the original manufacturer, we carry responsibility not only for molecular quality but also for the ethical footprint of our operations. Dedicated technical support staff address questions from all research backgrounds, including those handling hazardous, regulated, or cross-border shipments. Our QC and logistics teams remain focused on safe, on-time delivery and compliance with both domestic and international standards. Participation in voluntary chemical stewardship programs helps us keep information channels open and up to date, allowing for rapid response should regulations governing halogen- or sulfur-containing materials shift in any significant way.
We also uphold transparency by making detailed stability data available for every new batch, helping end users predict storage needs and prevent unexpected performance loss. This habit of full disclosure means users can plan synthesis schedules without risky guesswork. Upholding this practice over years, we have noticed fewer issues arising in post-delivery analysis and minimal disputes over technical interpretations. Our record for batch traceability and technical documentation reflects a direct manufacturer’s culture where accountability is non-negotiable.
Direct, honest dialogue drives the ongoing refinement of our 7-Chloro-2-iodothieno[3,2-b]pyridine. Success in research and development often rests on tightly coupled support from chemical manufacturers who understand more than sales quotas or stock volume. By keeping our doors open to custom inquiries, process feedback, and reported lab issues, we build products made for progress, not just purchase orders. Every year brings new technical challenges and end-use demands, which we take as opportunities to strengthen our systems and deepen the trust researchers place in our materials.
Our ongoing improvements in purity, packaging integrity, and customer service reflect our philosophy that chemical manufacturing supports far more than today’s sales figures—it supports the full spectrum of discovery and innovation across pharmaceutical, materials, and academic fields. The journey we take with 7-Chloro-2-iodothieno[3,2-b]pyridine, from reaction vessel to the customer’s bench, is marked by experimentation, learning, and a shared pursuit of reliable results.