|
HS Code |
656573 |
| Name | 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine |
| Chemical Formula | C7H3BrIN2 |
| Cas Number | 886362-36-3 |
| Appearance | off-white to light brown solid |
| Melting Point | 112-116°C |
| Purity | ≥98% |
| Solubility | DMSO, DMF, chloroform |
| Storage Conditions | Store at 2-8°C |
| Synonyms | 5-Bromo-3-iodo-pyrrolo[2,3-b]pyridine |
| Inchi | InChI=1S/C7H3BrIN2/c8-5-1-6-7(9)4(11-5)2-10-6/h1-2,11H |
| Smiles | C1=C(NC2=C1N=CC(=C2)I)Br |
As an accredited 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 5 grams of 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine, tightly sealed with hazard labeling and batch details. |
| Container Loading (20′ FCL) | 20′ FCL container can load approximately 10 metric tons of 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine, securely packed in drums. |
| Shipping | 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine is shipped in securely sealed containers, compliant with chemical safety regulations. It is packed to prevent exposure to moisture and light, and labeled per hazardous material guidelines. Shipping is typically done via ground or air by authorized carriers, accompanied by a Safety Data Sheet (SDS). |
| Storage | 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, preferably in a chemical storage cabinet designed for hazardous organics. Avoid exposure to heat or incompatible substances. Clearly label the container and follow standard laboratory chemical storage protocols. |
| Shelf Life | Shelf life: Store 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine in a cool, dry place; stable for at least two years. |
|
Purity 98%: 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine with purity 98% is used in the synthesis of pharmaceutical intermediates, where it ensures high yield and minimized side products. Melting point 207°C: 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine with a melting point of 207°C is used in solid-phase organic synthesis, where it provides thermal stability during reaction conditions. Molecular weight 316.93 g/mol: 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine with molecular weight 316.93 g/mol is used in medicinal chemistry research, where it allows precise stoichiometric calculations for analog development. Particle size <50 μm: 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine with particle size less than 50 μm is used in high-throughput screening assays, where it enhances dissolution and consistency in compound libraries. Stability temperature up to 120°C: 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine with stability temperature up to 120°C is used in heated batch reactions, where it maintains chemical integrity under elevated process temperatures. HPLC purity ≥99%: 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine with HPLC purity ≥99% is used in quality control labs, where it enables reliable analytical performance and reproducible assay results. |
Competitive 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Bringing 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine to life in our plant always gets chemists talking, because this heterocyclic molecule pulls its weight in real research and synthesis. Day in and day out, teams in the reactor room manage the nuanced steps for bromination and iodination, dialed in after years working with pyrrolo[2,3-b]pyridines. Consistency does not happen by accident; every batch faces scrutiny under chromatography and NMR to confirm purity and exact composition, since regulatory scientists and medicinal chemists alike want material free from ambiguous isomers or residual contaminants.
From a manufacturing floor, the heart of 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine’s value beats in its dual halogenation. Most bases in this class capture just a single halogen, so walking into a lab with this substrate unlocks more transformation options. Whether the goal is Suzuki, Sonogashira, or Buchwald-Hartwig cross-coupling, chemists can shape intricate targets by taking advantage of both aryl-bromide and aryl-iodide reactivities. Reproducibility remains a key conversation in scale-up meetings; starting with an authentic, high-quality intermediate like this means researchers sidestep unpredictable side reactions, stepping towards bigger and brighter scaffolds or active pharmaceutical ingredients.
Ask anyone on our technical team, and they’ll say how often the location of each halogen on the pyrrolopyridine core changes the reaction outcome. Small shifts in substitution patterns confuse downstream coupling steps, especially for applications in kinase inhibitor synthesis or building-block assembly. Chemists notice a big difference when using this true 5-bromo-3-iodo isomer instead of mixed or reversed halogen derivatives. In custom synthesis contracts, R&D units often specify the 5-bromo-3-iodo over the alternatives, focusing on direct connectivity, vital electronics, and optimal reactivity profiles. Whether assembling libraries or scaling a promising candidate, only the correct substitution truly moves the project forward.
Purity is not just a buzzword in this line of work. Those learning from experience see it in the way contaminated or mis-substituted feedstocks cause painstaking rework. With this compound, we guarantee only the 5-bromo and 3-iodo substitution—with batches reliably tested by HPLC and LC-MS. We push to keep extraneous halogenated species away because failed reactions in downstream chemistry cost more than starting materials. Each campaign on our reactor line delivers this product with a focus on fit-for-purpose quality, helping our collaborators and customers trust every gram.
Working with dozens of medicinal chemistry groups over the years, it’s clear how prized these dual-activated pyrrolopyridines have become as fragments for kinase inhibitor libraries, especially in early-stage screening. With the pharmaceutical need for molecular diversity growing, the dual halogenation supports chemists methodically altering substituents around the heterocycle and probing SAR landscapes. Unlike plain pyrrolopyridines or single-halogenated variants, this compound spurs the creation of novel analogues in less time. Efficiency in route scouting shines when starting from a true bromo-iodo scaffold—something not easily substituted by non-halogenated or singly halogenated rings.
Outside of pharma, our materials customers value 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine for introducing conjugated heterocycles into advanced organic electronics. The electron-rich core and two functional handles help researchers assemble pi-conjugated polymers, OLED emitters, or new chelating ligands. The fewer synthetic steps between basic building block and final functional device, the stronger the business case for keeping it on hand. Scientists in this branch of chemistry enjoy more flexibility using this substrate over basic halopyridines, both in batch production and in exploratory cycles.
For those manufacturing plant protection compounds, the pyrrolopyridine motif often figures in new crop protection scaffold design. The two halogen groups give agrochemical researchers the versatility to modify physical and biological properties through coupling or further functionalization, opening new doors in the pipeline for pest-resistant or environmentally adaptive actives. Agrochmical chemists often pull these specialty heterocycles as launching points for structure modifications impossible or uneconomic with monofunctional analogues.
Chemists know that not all halopyrrolopyridines perform equally. A laboratory using only 5-bromo or only 3-iodo analogues will soon face bottlenecks—either limited by lack of cross-coupling partners or running into reactivity mismatches. By offering both handles, we give synthetic chemists an upper hand with sequential orthogonal couplings, a feat that single-halogenated products struggle to manage without extensive protection-deprotection choreography. Both aryl halides bring unique reactivity profiles: iodides react under milder conditions, useful in cases sensitive to heat or harsh bases, while bromides permit different catalyst and ligand pairings, fine-tuning selectivity and speed.
Over the years, development teams have evaluated the impact of moving one halogen or the other to a different position. Slight shifts upend both regioselectivity in cross-coupling and biological readouts in medicinal chemistry screening. Even twin brominated or iodinated analogues present less versatile platforms—too reactive, too sluggish, or not distinctive for SAR purposes. Our 5-bromo-3-iodo product offers a perfect compromise in activation and practical handling, balancing chemical stability for storage and shipment with ready synthetic accessibility.
Beyond the lab, procurement teams pay attention to price, shelf stability, and consistency. Halogens placed at other positions may fall in price, but the wasted hours on cleanup, re-synthesis, or revalidation far outweigh any minor savings per kilo. As direct manufacturers, we focus on guaranteed performance, season after season, allowing buyers to sidestep supply chain interruptions common with hard-to-source research chemicals. By specializing in authentic, properly substituted material, we allow businesses to accurately forecast spend and experimental outcomes—something procurement and project management teams bring up repeatedly in their feedback.
Year after year, process improvements in our plant reflect what we have learned delivering this compound to customers with ever-rising expectations. Our operations have seen the necessity for sharp control over halogen source purity, process times, and reaction temperatures. It’s not uncommon for research requests to spike with little warning. Because we already manage logistics, storage, and packaging internally, we can react so researchers never lose momentum waiting on raw materials. Environmental health and worker safety also matter on the production side. We recovered, recycled, or neutralized countless kilos of spent halogen to minimize our impact, inspired by lessons from green chemistry and operational experience. The balance between throughput and stewardship means the next batch leaves as small an environmental footprint as possible, fitting with ongoing sustainability programs requested by many end-users.
Inside the plant, workers avoid shortcuts. Staff are trained not just to follow protocols but to spot early warning signs of impurity build-up, trace color or physical changes, and isolate unexpected side-products when they appear. Each kilogram produced faces not only analytical validation but also hands-on quality checks familiar to those who work regularly with advanced heterocyclic intermediates. With chemists and engineers collaborating daily, feedback loops between plant and lab troubleshoot issues before they leave the factory. This practical experience translates to far lower out-of-spec rates and faster response if technical questions arise.
Equipment wear and batch-to-batch variation get more attention with molecules this finicky. Changes in glassware, impeller coatings, or even atmospheric moisture can alter impurity profiles unexpectedly. Our teams document these factors closely, developing protocols that anticipate such shifts. Attention to detail at each stage—charging, reaction, workup, and final drying—delivers the substance at a level of consistency that downstream chemists rely on to avoid repeating multi-step syntheses because of small contaminants that throw off crystallizations or chromatography.
Having worked alongside chemists in scale-up, custom research, and pilot production settings, we know that subtle differences in chlorinated solvents, drying practices, or storage vessels can influence the shelf life and usability of 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine. Unlike commodity materials, this compound requires commitment to details most people overlook. By collaborating directly with users—commercial clients and R&D partners alike—we emphasize practical support, not just a product in a drum. Feedback from users often leads us to adjust crystal form, particle size, or packaging style to avoid static buildup or clumping, because what works in the lab pack does not always work at scale.
In the early days, demand for such building blocks was more sporadic, handled by specialty shops and small distributors. Now, research and commercial orders both depend on reliable global support. Over the past decade, project managers and purchasing leaders have made it clear that missing a delivery can cascade into lost time and sunk costs on much larger projects. As chemical manufacturers committed to long-haul relationships, we coordinate forecasting and logistics to keep supply resilient, including safety stocks and flexible distribution arrangements that shift with client needs.
One common question from both small labs and large production plants involves the compound’s shelf stability—especially in humid environments or after repeated sack openings. Our teams advise storing in sealed containers under inert atmosphere if possible, and have developed packaging solutions that minimize both moisture ingress and static buildup. For specific end users, we recommend tailored packaging volumes based on throughput rates: smaller, easy-pour bottles for analysts; larger bulk packs for parallel or scale-up work; and customized labels with traceability codes for regulated markets.
Another issue surfaces in scale transitions, as benchwork moves to pilot and production scale. Even robust molecules like this can develop unforeseen quirks—solubility shifts, filter clogging, or subtle impurities showing up only under certain workups. Our plant staff consult directly with end users to share practical methods—choice of antisolvents for crystallization, optimal suspension procedures, or best practices for recovery and storage. This ongoing partnership means less downtime and fewer surprises, especially for clients unaccustomed to handling advanced halogenated intermediates.
Changing regulatory frameworks add a layer of complexity once products move from research to preclinical or commercial pipelines. We keep ahead by internal reviews of regulatory changes, offering analytical support and batch documentation with provenance. Research programs now expect more than a certificate of analysis; they need detailed traceability, impurity breakdowns at ppm levels, and evidence that manufacturing meets ethical and environmental standards. Our teams update documentation and testing practices routinely, supporting customer audits and compliance efforts for projects that move towards regulated therapeutics or biocides.
There’s an ethos in this industry that goes beyond molecule-for-molecule exchange. Supplying 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine reliably, batch after batch, means direct engagement with every step of production, from sourcing raw materials to final packaging. Every team member has firsthand experience with what happens when a batch does not make spec—how quickly a missed impurity or unknown byproduct can spiral into lost time for a customer, and how reassuring it is for users when their feedback shapes our process.
The world of synthetic chemistry moves fast, often pushed by the next discovery or a new biological target. Standing behind the supply of advanced intermediates, we make sure that quality and communication keep pace. Over the years, partnerships shaped by shared challenges—unexpected reactivity, purity requirements, new downstream uses—have shaped our approach. Those who use our products are never just sales statistics. Their insights change how we formulate, handle, and deliver. The presence of both bromine and iodine on one pyrrolopyridine ring gives researchers flexibility, efficiency, and edge. Manufacturing it well brings its own reward: safe, reproducible, and reliable chemistry, made by hands that know what counts inside a bottle or drum.