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HS Code |
193962 |
| Name | 1H-pyrrolo[2,3-b]pyridine, 4-chloro-3-iodo- |
| Molecular Formula | C7H4ClIN2 |
| Cas Number | 1362295-36-8 |
| Appearance | light brown to brown solid |
| Smiles | ClC1=CC2=C(NC=C2I)N=C1 |
| Inchi | InChI=1S/C7H4ClIN2/c8-6-1-2-11-7(9)5(6)3-4-10-11/h1-4H |
| Solubility | Soluble in DMSO and DMF |
| Purity | Typically ≥97% |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Synonyms | 4-Chloro-3-iodo-1H-pyrrolo[2,3-b]pyridine |
As an accredited 1H-pyrrolo[2,3-b]pyridine, 4-chloro-3-iodo- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle, 5 grams, with tamper-evident seal, hazard labels, and chemical identification label: “4-Chloro-3-iodo-1H-pyrrolo[2,3-b]pyridine.” |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 1H-pyrrolo[2,3-b]pyridine, 4-chloro-3-iodo- involves careful drum arrangement, palletizing, and secure packaging for export. |
| Shipping | 1H-pyrrolo[2,3-b]pyridine, 4-chloro-3-iodo-, is shipped in tightly sealed, chemical-resistant containers to prevent moisture and light exposure. Packaging complies with DOT and IATA regulations for hazardous materials. Proper labelling and documentation accompany each shipment, ensuring safe and traceable delivery. Handle with appropriate personal protective equipment upon receipt. |
| Storage | 1H-pyrrolo[2,3-b]pyridine, 4-chloro-3-iodo- 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. Keep the container away from direct sunlight and sources of heat or ignition. Use appropriate personal protective equipment when handling, and clearly label the storage container. |
| Shelf Life | 1H-pyrrolo[2,3-b]pyridine, 4-chloro-3-iodo- typically has a shelf life of 2 years when stored cool, dry, and protected from light. |
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Purity 98%: 1H-pyrrolo[2,3-b]pyridine, 4-chloro-3-iodo- with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal byproduct formation. Melting point 189–192°C: 1H-pyrrolo[2,3-b]pyridine, 4-chloro-3-iodo- with melting point 189–192°C is used in medicinal chemistry compound libraries, where it provides stable handling and reproducible crystallization. Molecular weight 283.48 g/mol: 1H-pyrrolo[2,3-b]pyridine, 4-chloro-3-iodo- with molecular weight 283.48 g/mol is used in structure–activity relationship (SAR) studies, where it enables precise compound tracking and analytical validation. Stability at 25°C: 1H-pyrrolo[2,3-b]pyridine, 4-chloro-3-iodo- with stability at 25°C is used in long-term storage conditions for research materials, where it maintains chemical integrity over extended periods. Particle size <50 μm: 1H-pyrrolo[2,3-b]pyridine, 4-chloro-3-iodo- with particle size <50 μm is used in solid-phase synthesis techniques, where it improves reagent dispersion and reaction efficiency. High solubility in DMSO: 1H-pyrrolo[2,3-b]pyridine, 4-chloro-3-iodo- with high solubility in DMSO is used in biological assay preparation, where it allows for accurate dosing and homogeneous sample solutions. HPLC purity ≥99%: 1H-pyrrolo[2,3-b]pyridine, 4-chloro-3-iodo- with HPLC purity ≥99% is used in custom synthesis projects, where it guarantees reliable analytical performance and low impurity profiles. Storage under inert atmosphere: 1H-pyrrolo[2,3-b]pyridine, 4-chloro-3-iodo- stored under inert atmosphere is used in organometallic cross-coupling reactions, where it prevents oxidative degradation and ensures optimal reactivity. Low residual solvent (<0.2%): 1H-pyrrolo[2,3-b]pyridine, 4-chloro-3-iodo- with low residual solvent (<0.2%) is used in regulatory-compliant API manufacturing, where it meets stringent safety and purity requirements. Glass transition temperature <0°C: 1H-pyrrolo[2,3-b]pyridine, 4-chloro-3-iodo- with glass transition temperature <0°C is used in advanced material research, where it facilitates formulation of amorphous solid dispersions. |
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Anyone on the production floor understands that bringing 1H-pyrrolo[2,3-b]pyridine, 4-chloro-3-iodo- to a consistent and high purity isn’t simple work. We start from the core understanding that the demands for modern pharmaceuticals and materials research keep changing. Synthetic chemists are always asking for building blocks that can unlock new possibilities. Our drive to produce this compound grew straight out of the lab benches, where every step in the process means dealing with real-world challenges: scale-up issues, batch consistency, controlled atmospheric conditions, and safe handling of iodine-based intermediates. As a manufacturer, we live these challenges day in and day out.
The push for products like 4-chloro-3-iodo-1H-pyrrolo[2,3-b]pyridine comes from genuine needs. Over the past decade, more research teams have shifted their focus to nitrogen-containing heterocycles as key fragments in medicinal chemistry. Pyrrolopyridines, in particular, show up in kinase inhibitor exploration, agricultural research, and the design of advanced materials. What makes this particular derivative interesting for many is its dual halogen substitution. Introducing chloro and iodo groups together on a rigid, aromatic heterocycle doesn’t just add complexity for the synthesis—it opens up plenty of new routes for derivatization that aren’t so easily achieved using only traditional pyridine or pyrrole derivatives.
Buyers of 4-chloro-3-iodo-1H-pyrrolo[2,3-b]pyridine don’t just look for a simple bag of powder. Whether the destination is a research facility or a pilot synthesis suite, the end users care about the trace metal content and halide purity because these have a direct impact on downstream catalytic coupling reactions. Suzuki, Buchwald-Hartwig, and other palladium-catalyzed reactions begin to show significant yield losses with trace contaminants. Our experience tells us that keeping the iodine content controlled throughout packaging and storage safeguards our clients’ projects and budgets. There’s little room for compromise—an extra percent of moisture, off-spec melting point, or unseen decomposition products pile up as failed experiments and wasted resources in labs across the world.
We run each batch through a battery of checks—NMR, LC-MS, HPLC, and elemental analysis—because the fine details do matter. The entire team, from synthesis chemists to our quality assurance group, has faced the tension between higher yields and uncompromising quality standards. If a batch doesn’t meet our specifications, it gets held back. This way, we don’t risk introducing variables that would ripple down the line into a synthesis campaign.
Conversations with project leads often return to the theme of versatility. Compared to the less functionalized pyrrolopyridines, this molecule packs extra value for structure-activity research. The iodo group gives a vast toolbox for cross-coupling reactions—its reactivity far surpasses bromo- or chloro- analogues, with faster activation under milder conditions and broader compatibility with newer catalytic systems. On the other hand, the para-chloro group allows for further selective transformation or retention when selectivity matters in multi-step synthesis routes.
Pharmaceuticals benefit directly from this level of control. For example, kinase inhibitor programs utilize the electron-rich N-heteroaromatic ring system and often tweak substitution patterns to optimize pharmacokinetics and receptor binding. Using 4-chloro-3-iodo-1H-pyrrolo[2,3-b]pyridine as a scaffold provides a strong starting point for iterative rounds of SAR, letting chemists bolt on different aryl or alkyl groups, thanks to the unique positions of halides.
From our experience supporting scale-up projects, being able to offer this compound consistently helps move programs along. Rarely does a single fragment open such a range of downstream transformations; most other aromatic heterocycles—like a simple pyridine—don’t allow this degree of selective halogen manipulation. Research teams often combine this core with boronic acids, alkynes, or amines for tailored library construction. Those who have wrestled with less reactive bromo-derivatives see real gains in yield and selectivity using the iodo variant.
Handling compounds with dual halogen substitution challenges our logistics operations as much as it does our synthetic unit. Like many other high-value intermediates, this product requires close control of humidity and light during storage. Iodinated organics can suffer slow degradation over time, leading to coloration and unwanted side products. Drawing on past recalls and customer feedback, our packing and shipping standards reflect hard lessons learned. We store the material under an inert atmosphere and ship only in certified containers that resist iodide leaching and minimize headspace.
Safety isn’t just a line in a brochure for us. Everyone moving, packaging, or cleaning up around this intermediate handles it with gloves and full ventilation. Nobody wants to deal with volatile halogen vapors or accidental contact, so our team trains regularly on the hazards specific to both chloride and iodide organics. Overexposure risks aren’t always obvious to outside observers, but we see what a lapse looks like, and we don’t cut corners.
Clients sometimes ask about shelf stability—how well does the compound hold up at room temperature over weeks or months? In our experience, purity above 98 percent endures at least one year under dry nitrogen, with no loss in active halide content. Left open, though, iodoarene degradation creeps in slowly; spotted it often enough by changes in appearance and HPLC signals. We invested in dedicated cool storage after catch a few borderline batches in routine QA checks. That’s the cost of learning alongside the market, and the lesson is clear: better control, fewer surprises.
For many chemists, the product needs to show up ready to dissolve in their favorite solvents—usually DMF, DMSO, or the common chlorinated solvents. We take product solubility seriously because stubborn residue at the start can sabotage fine work farther down the line. Our team filters every lot to ensure tiny particulates don’t interfere with reactions, especially where stringent mass spec requirements exist.
Compared to other halogenated pyrrolopyridines, this compound balances reactivity with manageability. Brominated analogues frustrate researchers with their sluggishness in palladium-catalyzed couplings; those that swap iodine for fluorine lose the breadth of subsequent modification. Chloro-only derivatives trade away the easy installation of larger or more sensitive groups. In practice, users want the flexibility to pull off one halogen selectively and tweak the scaffold while maintaining enough reactivity for downstream steps. Our product stands out because it supports those goals—no more compromises between selectivity and yield, no more lengthy workaround syntheses.
Most of the time, questions come back to reliability. What sets product from a genuine manufacturer apart from resellers isn’t just the paperwork—it’s a knowledge of the process, batch history, production quirks, and the warning signs one picks up after countless runs. Our clients rely on us for answers: which solvents work best, how to minimize by-products, and why they’re seeing an unusual NMR shift. Feedback from users shapes the way we handle and package things. In one memorable case, a site flagged a stubborn contaminant during a scale-up. We got on a call, dug into both our analytics and theirs, and found that small shipping delays resulted in temperature swings that drove a side reaction. After that, we switched to vacuum-sealed cold packs for every mid-summer shipment.
Trust doesn’t grow from standard paperwork. For us, manufacturing is personal, and that responsibility carries over to our support before and after each order leaves our gate. Customers often reach out when troubleshooting experimental failures; we’ve sent follow-up analyses, confirmed lot lineage, even reworked material at our own cost to meet critical deadlines. Our chemists keep records of every tweak made, every unexpected impurity tracked, every improvement added to the workflow. Over the years, these details have stacked up as a huge knowledge bank, helping us steer clear of familiar pitfalls and keep delays short when issues crop up.
One defining difference working as a direct manufacturer is that we see the entire journey of this compound. Handling every stage, from raw material sourcing through to final QA, gives us perspective that goes well beyond trading. Sourcing high purity iodine and chlorinating agents, for example, means dealing with volatile pricing, regulatory paperwork, and occasional customs headaches. Sometimes, lengthening lead times upstream make the critical difference to a customer’s timeline. We’ve learned to overstock raw materials in anticipation of global supply chain disruptions, based directly on signals from regular purchasers and academic labs. In an era of supply uncertainty, our ongoing relationships with chemical suppliers and logistics partners make shipment delays less likely and emergency orders possible.
No manufacturing process ever stands still. Over the years, requests have pushed us to refine purification, drying, and packing processes to improve results in end-use applications. Unexpected feedback often drives process changes; a synthetic challenge faced in one customer’s medicinal chemistry group has often led us back to our own reactors for improved process optimization. From time to time, this means redesigning steps or switching catalyst systems entirely to avoid troublesome side-product formation. We’ve even rolled out pilot runs for ultra-high-purity grades at the request of a collaborative research project. These extra efforts rarely show up in standard specs, but for frequent buyers who know our track record, the added trust carries through every order.
One philosopher-chemist once remarked that “the route is the reaction.” We see the truth of that every day. When a client wants to try an unorthodox coupling or needs a custom halogen ratio, we’re already set up to adjust our workflow, rather than insist on rigid one-size-fits-all solutions. Direct feedback flows swiftly from the bench to the plant floor. Sometimes this means scrambling to adjust drying conditions, running extra purification trains, or hand-checking the final output under strictest standards. This helps reduce batch failures and keeps valuable research on track, saving time and money for everyone involved.
The open exchange of information also means that we pass along real-world tips, not just boilerplate handling instructions. For example, a few years back, a customer’s team struggled with unexplained reactivity loss in large batch couplings. After some digging, it turned out their workup solvents had traces of peroxide—something we started to check for as part of our outgoing QA soon after. These hard-won lessons are part of the package when dealing directly with a dedicated manufacturing partner, instead of sitting at arm’s length through third-party channels.
In our section of the specialty chemical manufacturing world, indirect supply routes can introduce unnecessary risks—untracked substitutions, commingled lots, or repacked material with unclear history. Direct manufacturing means full access to batch data and process controls. More importantly, it means that questions and problem-solving happen without finger-pointing between intermediaries. Our production team keeps continuous logs; details of starting material origins, reaction temperatures, filter types, and even environmental data carry forward from raw material intake to final shipment. This level of documentation isn’t academic—it’s essential for reproducibility, especially for regulated or patent-driven research.
Another distinct point comes from our ability to balance batch sizes. For large clients, the ability to ramp up from analytical to kilo-scale synthesis with consistent product profile offers a head start, bypassing supply bottlenecks that plague limited-stock resellers. At the same time, researchers benefit from the availability of multiple lot sizes rather than being limited to a single format or grain. Adjusting production scale for custom needs allows us to control the process every step of the way.
Whereas the broader market might rely on generic brokers, our hands-on control keeps fraudulent or off-spec product out of circulation. Once, a batch flagged for abnormal NMR signals got tracked to a supplier error halfway through the chain—by owning and investigating our production, we rapidly isolated and resolved the problem, saving a client from costly project delays. This approach has also let us roll out batch-specific documentation and analytical support, which keeps end users confident in their results and lets them trace any anomaly back to real process causes.
The global drive for novel therapeutics, agrochemicals, and advanced materials places growing demand on reliable specialty chemicals. Each year, scientific literature reports new molecules and bioactive scaffolds built by agile manipulation of halogenated pyrrolopyridines. Keeping one step ahead means learning from both success and failure, listening closely to feedback from customers, and leveraging each experience into refined manufacturing method.
We don’t just measure our success in tons of output or the speed of fulfillment. The real value comes from buyers who come back time after time, often with special requests, timeline crunches, or questions that other suppliers won’t touch. In one major research partnership, we devoted plant time to run micro-optimized batches for structure-activity studies, each tuned for slightly different halide loadings. Those seemingly small changes in the workflow allowed the research team to publish groundbreaking SAR data ahead of schedule. Everyone benefits from trusted relationships, honest communication, and deep product understanding.
Manufacturing 4-chloro-3-iodo-1H-pyrrolo[2,3-b]pyridine in today’s world means more than stamping a model number on a container. It demands an ongoing commitment to improvement, quality, safety, and shared progress. Our daily work brings us face-to-face with every challenge, from chemistry to logistics, ensuring that each batch delivers more than just a reagent—it opens new doors for research, industry, and discovery.