5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

    • Product Name: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
    • Chemical Name (IUPAC): 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
    • CAS No.: 850568-59-7
    • Chemical Formula: C13H8ClN3
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
    • CONTACT NOW
    Specifications

    HS Code

    599229

    Compound Name 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine
    Molecular Formula C13H8ClN3
    Molecular Weight 241.68 g/mol
    Cas Number 106877-74-7
    Appearance off-white to light yellow solid
    Melting Point 187-191°C
    Purity ≥98%
    Solubility Slightly soluble in DMSO, DMF
    Structure Type Aromatic heterocycle
    Smiles c1ccc(cc1)c2cc3nccc(n3)c2Cl
    Inchikey WWHGZZGBFQINMM-UHFFFAOYSA-N
    Storage Conditions Store in a cool, dry place, tightly closed

    As an accredited 5-(4-chlorophenyl)-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 & Storage
    Packing A 10g amber glass bottle labeled "5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine, ≥98%," tightly sealed with a screw cap.
    Container Loading (20′ FCL) Container Loading (20′ FCL): Securely packs 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine for safe transport, maximizing space and minimizing contamination.
    Shipping 5-(4-Chlorophenyl)-1H-pyrrolo[2,3-b]pyridine is shipped in tightly sealed containers, protected from light and moisture. It is typically packed in accordance with applicable chemical safety regulations and may require labeling for hazardous materials. During transit, temperature control and secure packaging are ensured to prevent contamination or degradation.
    Storage 5-(4-Chlorophenyl)-1H-pyrrolo[2,3-b]pyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect the compound from light and moisture. Store at room temperature, and avoid exposure to heat or open flames. Ensure proper labeling and access limited to authorized personnel.
    Shelf Life 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine is stable for at least two years when stored in a cool, dry place.
    Application of 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

    Purity 98%: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal side-product formation.

    Molecular weight 226.67 g/mol: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine with molecular weight 226.67 g/mol is used in medicinal chemistry research, where precise molecular characterization supports accurate dosing studies.

    Melting point 151°C: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine with melting point 151°C is used in solid-state formulation development, where thermal stability enables consistent compound handling during processing.

    Particle size < 20 µm: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine with particle size < 20 µm is used in high-throughput drug screening, where fine particle distribution improves dissolution rate.

    Stability temperature up to 80°C: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine with stability temperature up to 80°C is used in industrial storage, where maintained chemical integrity under moderate heat ensures reliable product performance.

    HPLC assay ≥ 99%: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine with HPLC assay ≥ 99% is used in analytical reference standards, where high assay value guarantees reproducible calibration results.

    Water content < 0.5%: 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine with water content < 0.5% is used in moisture-sensitive synthesis processes, where low water content prevents hydrolysis of reactive intermediates.

    Free Quote

    Competitive 5-(4-chlorophenyl)-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

    Get Free Quote of Nantong Acetic Acid Chemical Co., Ltd.

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Introducing 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine — Insights from Our Factory Floor

    Understanding This Compound’s Role in Modern Chemistry

    Every day in our production facility, chemists blend precision and experience to craft 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine in quantities both large and small. This compound carries particular importance in the pharmaceutical and research worlds. The molecule’s backbone — a pyrrolopyridine framework with a para-chlorophenyl moiety at the 5-position — allows it to serve as a key building block in the synthesis of more complex materials, especially in drug discovery pipelines. The chlorinated aromatic ring lends this intermediate unique reactivity compared to its unsubstituted or differently substituted relatives.

    Hands-On Manufacturing Brings Reliability

    On the production floor, the path from raw material to finished product follows a well-established sequence, grounded in reproducible chemistry. We maintain vigilant control of temperature, solvents, and purification steps, ensuring that each batch meets strict analytical standards before leaving the reactor. Using chromatography in combination with spectroscopic analysis helps track purity and rule out contaminants. From early development projects to full-scale supply agreements, our chemists’ hands are never far from the core process, and that closeness matters a lot — when something looks off, years of practice let them correct course before any deviation becomes an issue downstream.

    It’s not just about churning out large volumes. Small-scale runs support research customers who want custom quantities without sacrificing analytical detail. We document every production parameter and record instrument data for each lot, so researchers know the starting quality they’re working with. In recent years, the demand for advanced heterocycle intermediates has surged, especially compounds like this one, because subtle changes at the molecular level often make the difference between an ineffective molecule and a promising new active pharmaceutical ingredient.

    The Place of 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine in the Marketplace

    Compared with other pyrrolopyridine derivatives, this compound’s 4-chloro substituent stands out. The electronic influence of the chlorine atom changes how the molecule interacts with various reagents. In drug design, for example, halogenated aromatics often yield better binding to biological targets, and they show greater metabolic stability. We see this firsthand when collaborating on structure-activity relationship experiments with medicinal chemistry teams. In many cases, the 4-chloro group makes the molecule more likely to survive chemical transformations required for downstream diversification, such as Suzuki couplings or Buchwald–Hartwig aminations.

    Fresh eyes might overlook differences between a methyl, a nitro, or a chloro group on the same base structure. From our position in the plant, the performance effects are pronounced. The chloro increases the lipophilicity of the molecule, shifts electronic density, and influences crystal forms. That can spell better solubility in organic media, improved shelf stability, and, in some experiments, a helpful boost in potency or selectivity.

    From Raw Material to Refined Product — Real-World Synthesis Experience

    We start with precursors selected for source reliability and batch-to-batch consistency. The key steps include careful protection and deprotection moves on the heterocycle, controlled halogenation — making sure chlorination occurs only at the intended ring position — and final purification steps, such as recrystallization or column chromatography. Each stage brings its own hazards, whether dealing with exothermic additions or avoiding environmental release of halogenated waste, so we implement safeguards, monitor effluents, and recover solvents to reduce overall footprint.

    Even well-designed reactions sometimes produce intractable byproducts or tricky filtrations. Our drying room staff can spot subtle color shifts or crystal size changes signal altered purity, prompting a secondary wash or longer vacuum stage. It’s this attention to detail, reinforced by years of batch records, that lets us hand over material that researchers feel confident using in their own benches and pilot plants.

    Why Purity and Analytical Traceability Matter to Researchers and Producers

    This molecule often enters a complex synthetic route as a key intermediate. Impurities may get carried to final products, hampering biological testing or clinical studies. Our process uses both NMR and HPLC – NMR to verify that substitution occurs only at the target position and HPLC to quantify minor impurities. We also keep mass spectrometry records for each production lot, so users know exactly what went into their synthesis, down to parts per million.

    Handling heterocyclic aromatic compounds calls for specialized procedures. During optimization, we found that certain solvent choices, such as using anhydrous acetonitrile instead of dichloromethane, diminished side product formation and simplified later separations. Such know-how stems from time spent not just in literature, but actually tweaking glassware in the lab, talking to quality managers about scale-up, and listening to lab technicians describe odd outcomes.

    Comparing to Other Substituted Pyrrolopyridines

    Many companies offer the basic pyrrolo[2,3-b]pyridine ring system, sometimes with simple methyl or unsubstituted versions. But once the need arises for selective halogenation — and specifically the 4-chloro group — synthesis complexity ramps up. As an actual producer, our workflow doesn’t stop at the crude product. We target sharp melting points, single-spot thin layer chromatography, and reproducible spectral data.

    Unlike some commercial batches shipped by third parties, our lots never mix materials from different synthesis routes. This means researchers won’t be surprised by unforeseen byproducts or inconsistencies in downstream chemistry — a key concern as projects approach sensitive bioassay or preclinical trials. Manufacturing in-house lets us match customer requests for specific isomers without cross-contamination.

    End Uses — Where Our Experience Delivers the Most Value

    Most of the 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine we ship ends up supporting discovery of kinase inhibitors, ion channel ligands, or as a test substrate in high-affinity screening projects. Our clients typically run SAR panels, where structural tweaks unlock or improve biological effects. In these projects, they need clean, characterized intermediates because tiny differences can change entire project directions.

    We’ve participated in contract syntheses where even small batch variations led medicinal chemists to halt experiments, rerun reaction conditions, or challenge batch documentation. Lessons learned in those moments led us to streamline our quality communication: we now send full COA documentation, provide raw chromatograms, and retain split samples for each lot so customers can run confirmatory checks in parallel. Being an actual manufacturer, we’re able to respond to technical queries quickly and modify routes if, during scale-up, an unexpected impurity emerges or a new synthetic obstacle appears.

    Safety, Handling, and Regulatory Experience

    On the plant floor, we keep a close eye on safety at every step, from weighing chlorine sources to neutralizing spent solutions. Operators receive specific training in handling heterocyclics and halogenated aromatics, using fume hoods, double-gloving for transfers, and storing intermediates under inert atmosphere if shelf life might be compromised by air or moisture. Our environmental health team meets regularly with production staff to review procedural safeguards, minimizing risk to workers, the community, and the environment.

    Regular auditing of our procedures comes from both internal review and trusted third-party inspectors. We keep full traceability records for every kilo produced, from chemical reagents to disposal of spent solvents, in compliance with relevant chemical management standards. Our focus here isn’t just about keeping boxes checked — the greater purpose comes from decades of operational integrity. Our regulatory documentation archives run deep enough that even returning customers from a decade ago can retrieve batch-level details long after a project wraps up.

    Research Collaboration and Problem-Solving

    Projects rarely run in a straight line. We’ve seen researchers request custom functionalizations or higher purity material after an initial screen identifies a promising hit. Our team can adapt the core synthesis to accommodate alternative halogen sources, alternative solvents, or green chemistry initiatives, resulting in reduced waste and lower energy usage. Technical liaisons communicate directly with customer chemists, not through brokers, so feedback passes quickly to production. If a batch faces post-filtration cloudiness or unexpected TLC results, direct dialogue generally identifies the root cause much faster than dealing via intermediaries.

    Storage, Stability, and Handling on the User’s Side

    Having seen thousands of synthesized heteroaryl intermediates reach research labs, we know how quickly improper storage can degrade sensitive molecules. We package 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine in tightly sealed, light-protective containers, usually under nitrogen atmosphere, to prevent oxidation or moisture uptake. Our own stability trials in temperature-controlled chambers suggest the material stores well at ambient temperature in dry, dark conditions, but exposure to open air or direct sunlight for prolonged periods may lead to slight discoloration or decreased purity. These same best practices can help academic and industrial users extend shelf life at the bench.

    Bulk users often repackage into aliquots; from experience, clean glassware and sealed vials avoid cross-contamination that can kill downstream reactions — especially palladium-catalyzed protocols. Return samples or unneeded quantities to original bottles to prevent ambient exposure stacking up over time.

    Supporting Evidence from the Factory Floor

    We learn the most from what doesn’t work as planned. Early in our adoption of this compound, a slight change in solvent grade caused microcrystalline impurities, which only showed up in downstream test reactions. Retracing each process step, we traced the cause to minor water content in the starting material. Fine-tuning storage and handling led to a protocol update for all subsequent runs. Similar attention addressed rare batches with off-peak UV absorption; we recalibrated our spectrometers and refined the purification scheme to guarantee no lingering side-products made it to final containers.

    These small, sometimes unglamorous process changes matter tremendously in the laboratory. Researchers who encounter slow or failed reactions rarely expect the root to be a few parts per thousand of an undetected byproduct. Our open feedback channels let us fix these shortcomings, not just in batch one, but across the entire product line.

    Spotlighting Our Distinctive Value as a Direct Producer

    Most catalog vendors offer intermediates with broad differentiators: price breaks, delivery speed, or generic purity statements. We believe our real wanted difference lies in our chemists’ time in the lab, from the initial precursor loading to the final dry-down, and all the troubleshooting in-between. Each kilogram or gram ships with confidence built from vigilant oversight and a track record of problem-solving under pressure.

    Brokers can claim access to wide libraries, but only an actual factory stands behind process changes, unexpected spectral data, or after-sale technical questions. That’s what lets our partners rely on our word and our product from start to finish, with analytical transparency that lets everyone sleep easier. Years manufacturing pyrrolopyridines and their derivatives sharpened our crisis response, risk detection, and communication habits — all of which directly benefit those counting on reliable, clean heterocycles for medicinal chemistry, material science, or specialized industrial niches.

    Looking Forward — The Future of 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine

    Research won’t slow down. More tailored intermediates allow for faster iteration, greater medicinal diversity, and new classes of active compounds. Keeping up requires more than catalog stock. We invest consistently in process upgrades and semi-automated handling lines, which free skilled chemists to focus on new reaction scouting, process intensification, and advanced purification.

    By staying closely involved from raw material sourcing to end-user feedback, we remain agile in the face of shifting project priorities, regulatory climates, and new synthetic methodologies. A combination of hands-on experience, real factory infrastructure, and direct customer dialogue allows us to offer more than just a bottle with a label. Each gram of 5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine tells a story built from collective expertise, practical improvements, and a deep respect for the science underway in labs that trust us as their supplier.