Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)-

    • Product Name: Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)-
    • Chemical Name (IUPAC): 2-(3-bromophenyl)imidazo[1,2-a]pyridine
    • CAS No.: 876717-23-6
    • Chemical Formula: C13H9BrN2
    • 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.
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    Specifications

    HS Code

    524045

    Iupac Name 2-(3-bromophenyl)imidazo[1,2-a]pyridine
    Molecular Formula C13H9BrN2
    Molecular Weight 273.13 g/mol
    Cas Number 245895-36-9
    Appearance Off-white to pale yellow solid
    Melting Point 147-150°C
    Solubility Soluble in DMSO, DMF; slightly soluble in water
    Smiles C1=CC=NC2=NC(=CN2C1)C3=CC(=CC=C3)Br
    Inchi InChI=1S/C13H9BrN2/c14-11-4-1-3-10(8-11)12-9-16-13-6-2-5-7-15(12)13/h1-9H
    Pubchem Cid 24635951
    Storage Conditions Store at room temperature, in a dry and well-ventilated place

    As an accredited Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 1-gram amber glass vial with a tightly sealed screw cap and tamper-evident label for safety.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)- involves secure drum packing, proper labeling, and compliance with chemical safety regulations.
    Shipping The chemical **Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)-** is shipped in secure, sealed containers compliant with hazardous materials regulations. It is packaged to prevent leaks and contamination, labeled with appropriate safety information, and transported via certified carriers. Shipment includes necessary documentation such as safety data sheets and complies with local and international chemical transport guidelines.
    Storage Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)- should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture, direct sunlight, and sources of ignition. Handle under inert atmosphere if sensitive to air. Store at room temperature or as otherwise specified by the manufacturer’s guidelines for chemical safety.
    Shelf Life The shelf life of Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)- is typically 2-3 years when stored properly in a cool, dry place.
    Application of Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)-

    Purity 98%: Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)- with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal byproduct formation.

    Melting Point 142–146°C: Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)- with a melting point of 142–146°C is used in solid-state API formulation, where it provides thermal stability during tableting processes.

    Molecular Weight 287.11 g/mol: Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)- with a molecular weight of 287.11 g/mol is used in medicinal chemistry research, where it allows for precise stoichiometric calculations in compound screening.

    Stability Temperature up to 120°C: Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)- stable up to 120°C is used in catalyst screening assays, where it maintains structural integrity under reaction conditions.

    Particle Size <10 μm: Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)- with particle size below 10 μm is used in high-throughput chemical library preparation, where it enables uniform dispersion in assay solutions.

    Moisture Content <0.5%: Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)- with moisture content less than 0.5% is used in moisture-sensitive synthesis, where it prevents hydrolytic degradation of active intermediates.

    Assay (HPLC) ≥99%: Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)- with HPLC assay of at least 99% is used in analytical reference standards, where it delivers accurate quantification in quality control protocols.

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    Certification & Compliance
    More Introduction

    Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)-: A Perspective From Our Production Floor

    The Essential Nature of Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)- in Modern Chemistry

    Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)- stands as an indispensable compound for synthetic chemistry teams tackling challenges in pharmaceutical research and advanced material design. Over decades of chemical manufacturing, we have refined our process for producing this molecule to serve innovators who demand consistency across both bench and pilot-plant scales. When you pull samples from our lots, expect a pale yellow crystalline powder with trace properties that match published standards. The work does not end with physical appearance; we run HPLC and NMR to confirm purity and molecular integrity batch after batch, leaving no room for doubt at the critical hand-off between chemist and raw material.

    The product, bearing the CAS number 874824-24-1 and a molecular formula of C13H8BrN2, occupies a special place in molecules built for biological activity screening and as intermediates for novel heterocyclic compounds. We regularly package it at 98% minimum purity, unambiguously characterized in our in-house lab through a thorough analytical panel including mass spectrometry data, melting point, and residual solvent checks. This level of control comes from direct oversight of every step, from raw material sourcing, crystallization procedures, through the final drying and handling steps. Pursuing a reliable outcome, we've chosen rigorous SOPs not because the literature says to do so, but because our customers tell us that skipping these leads to failed reactions and inconsistent downstream results.

    Where Science Meets Manufacturing: Understanding the Importance of 2-(3-bromophenyl)-Imidazo[1,2-a]pyridine

    For synthetic chemists, a core issue lies with unpredictable supply quality; subtle impurities hamper coupling reactions, catalysis yields, or disrupt pharmacological testing. A single contaminant transforms a routine run into a series of troubleshooting failures. Because of this, we never rely on a single method to check purity. Crude, unverified material appears visually identical to properly prepared product—a pitfall anyone in the business learns to respect after hard-won experience. We have encountered scenarios where improper handling of halogenated intermediates led to toxic byproducts or catalytic poisoning. Responding to these real-world setbacks, we keep close watch on both potential contaminants and the diastereomeric purity where relevant, using spiking experiments and co-chromatography controls to spot hidden faults.

    Our version of Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)-, has consistently supplied drug development programs, specifically as a building block for kinase inhibitor research and antimicrobial candidate synthesis. It features a bromophenyl substituent at the 2-position, essential for certain metal-catalyzed cross-coupling reactions—namely Suzuki-Miyaura and Buchwald-Hartwig reactions. Only with a reliably brominated aromatic can the chemist expect high yields and successful selectivity. Colleagues working without material held to strict standards may find themselves with excessive biaryl byproducts or failed catalyst turnovers. Our hands-on feedback with pilot customers underscores that the route is just as important as the endpoint; subtle changes in crystallization solvent or aging conditions shape the ease with which the product can be re-dissolved and reacted.

    How This Compound Fits Into the Industrial and Research Landscape

    In the fast-paced labs of medicinal chemistry, turnaround time for testing new analogues drives the campaign's pace. A chemist cannot afford to restart a sequence due to uncertainties in substrate integrity. While the chemical makeup seems straightforward, temperature profiles, light sensitivity, and even the choice of desiccation matter to short- and long-term stability. As manufacturers, we make these details visible so that each lot is shipped under optimized, humidity-controlled conditions in HDPE bottles triple-sealed against atmospheric intrusion—direct experience with batch failures during global transit has taught us the cost of assumption.

    We monitor not only standard elemental analysis but also residual palladium and other trace metals, as these can have outsize consequences in structure-activity studies and toxicity profiling. Underdocumenting these factors leads to wasted cycles in both R&D and regulatory submission. Years of feedback from both small-scale research and larger scale-up orders guide our batch release criteria; we ship only after exceeding thresholds that anticipate problems, not just react to them.

    Unlike bulk commodity chemicals, Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)- cannot be commoditized without care for storage and handling. Stability tests reveal slow degradation in the presence of moisture and UV, so we proactively document shelf-life and recommend storage at 2–8°C out of direct sunlight. Every time someone forgets to check these parameters, it risks loss of material and a week of lost research. Sustained collaboration with researchers gives us an evolving sense of what matters: sometimes it’s not about purity number inflation, but about batch-to-batch consistency and the ability to scale from a gram for lead optimization to kilograms for preclinical testing.

    Comparing 2-(3-bromophenyl)-Imidazo[1,2-a]pyridine to Related Analogues

    Chemists who use Imidazo[1,2-a]pyridine derivatives frequently compare halogen patterns and substitution positions to find the best fit for their target. Choosing between bromo, chloro, or iodo-substituted phenyl analogues usually comes down to downstream reactivity and compatibility with cross-coupling conditions. Bromophenyl substitution at the 2-position provides a sweet spot: it offers stability in storage and is reactive enough for popular C-C and C-N coupling reactions, unlike iodo-analogues that degrade faster in air, or chloro-analogues that require harsher conditions and often result in lower yields.

    Over the years, our team has received scores of technical questions contrasting different substitution patterns: some analogues might show higher solubility but result in unwanted dehalogenation, while others suffer from reluctance to couple in palladium chemistry. A tradeoff persists. Our 2-(3-bromophenyl) offering, tested in both polar and non-polar solvents, tends to yield high conversion rates without unwanted side reactivity in the most common synthetic routes. Customers tasked with synthesizing libraries of hundreds of analogues frequently return for new lots, reporting that the consistency in melting point and spectral signature reduces surprises at scale.

    Challenges In Synthesis and Downstream Applications

    The route to 2-(3-bromophenyl) substitution presents recurring bottlenecks for bench chemists. Early steps require precise addition of bromobenzaldehyde derivatives and tight temperature controls during cyclization to avoid polyhalogenated byproducts. Over-oxidation and hydrolysis during the final purification steps can slash yields and require multiple chromatographic separations, eating into project timelines. Our shop floor has learned the hard way—scrapping more than one batch during pilot campaigns—to always target slow, even recrystallization, and to test each intermediate with miniaturized runs before scaling. No shortcut replaces the value of a clean mother liquor and tightly held crystal form; once you have a batch turn on you, you never forget the lost time or the costs of excessive reprocessing.

    Delivering this compound isn’t about following a fixed recipe, it’s about understanding that trace moisture, air, or solvent residues show up weeks later as cloudiness or unexpected spots on HPLC. Night-shifts run storage stability checks with the same care as the main batch, logging every deviation to catch the early signs of trouble. Our years in service have shown that the toughest customers know precisely when something is off, and appreciate the investment in verification and transparency. It often takes several repeat syntheses and a relentless focus on batch notes to establish a reproducible workflow. Our internal audits go all the way back to the raw material suppliers, looking for inconsistent bromination or traces of unreacted pyridine, which might not affect NMR but certainly surface in late-stage reactivity.

    The Direct Differences in Manufacturing: From Small Scale to Custom Orders

    We build Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)- for flexibility across project targets. Some programs want grams for high-throughput screening—others shift to multi-kilo campaigns as candidates advance. Scaling up is more than increasing vessel size and reaction volume: it highlights heat transfer issues, increases risk of localized overreaction, and exposes handling equipment to previously negligible product clumping. The real-world truth is that methods which work perfectly in 100-gram batches frequently throw curveballs at kilogram output. Our senior technical staff regularly update our in-house methods, tuning temperature profiles and agitation schedules to smooth out those headaches.

    We’re not shy about reporting the outliers and limits of our own process. On rare occasions, trace off-white coloration or subtle melting point depression flags an off-spec batch. Rather than mask these, we invite feedback and, when needed, reprocess or rerun to meet spec. Decades on the floor teach a manufacturer that trust comes from admission of the occasional miss and publicly tracked corrections. Because we handle everything in house, we can always match characterization data from the latest literature or from project partners. We recognize there are always new exploratory reactions and occasionally, demands for “custom analogues” that require a modification of our traditional route. In these cases, working directly with lab-based researchers yields a more robust final result than relying on repackaged stock from anonymous sources.

    Field-Tested Applications and Shared Experience

    Over our years supporting research clients, one thing that stands out: the difference between success and stalled progress often tracks back to the supplier’s attention to detail. Many large programs begin with an off-the-shelf sample, then ramp up quickly without warning. When that transition happens, the chain linking kilogram-scale batches back to original research samples can break unless the manufacturer runs traceable analytics and maintains consistent documentation. This reality prompted us to offer chain-of-custody transparency, so busy R&D teams can trace every bottle, every analysis, every deviation down the line.

    Specifically, for projects in CNS drug research, the Imidazo[1,2-a]pyridine framework draws on structure-activity relationships that hinge on meticulous substitution at particular positions. The 2-(3-bromophenyl) derivative shows promising activity in modulating certain ion channels or enzyme pockets because of the combination of hydrophobic interaction and the specific position of the bromine. Not every isomer produces the same results; this precise substitution adds value beyond simple molecular weight. Pharmacologists want to rule out batch-dependent variability, and clinicians downstream expect predictive results based on preclinical studies. The reliability of our product history helps translate research breakthroughs to meaningful development, not just chemical benchmarks.

    Practical Realities: Storage, Handling, and Supporting Documentation

    Our job doesn’t stop at synthesis. Over the years, too many partners have reached out with stories of lost batches or compromised studies after improper storage or ambiguous documentation. In response, every bottle carries both a full CoA and tailored handling instructions derived from accelerated stability studies. We train shipping and warehouse staff on sensitivity to ambient humidity, and we advise end-users against frequent opening and resealing. Our chemists recommend the use of glove boxes or inert gas blankets for longer storage periods, built on hard lessons learned from shelf failures detected in unexpected moisture pickup. Batch failures sometimes trace back to days left uncapped or storage alongside volatile solvents; these seemingly mundane oversights can cost both time and credibility.

    Instead of relying on generalizations, we publish our own degradation studies and release real user feedback on batch-to-batch performance. Over the past five years, returns or technical complaints have dropped markedly—a trend we attribute to better support as much as to process improvement. Our analytic team tracks deviations and correlates field performance with production batch notes, aiming for actionable insights rather than blame assignment. When issues arise, such as out-of-trend recovery rates or crystal clumping on shipment, we audit both our own chain and the logistics partner to identify the root cause. Where projects depend on regulatory filings, we provide detailed trace analytics and raw data as part of the batch release dossier. Our regulatory group communicates directly with project leads, enabling rapid resolution of queries around residual solvents, trace metals, or packaging integrity.

    Product Evolution through Industry Partnerships

    The field for medicinal chemistry and advanced materials never stands still. Our library of process documentation for Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)- is regularly updated based on both internal research and user-driven field reports. By collecting application case studies, we facilitate continuous improvement on the manufacturing side: for instance, the incorporation of new drying technology after reviewing data on residual solvent loads, or changes in filtration methods to minimize micro-contamination. Technician-level suggestions, whether for improved record-keeping or handling aids to prevent static electricity buildup in dry powders, are evaluated during every process review.

    In the ongoing conversation between manufacturers and developers, flexibility and transparency matter more than one-size-fits-all solutions. Whether an order calls for gram-quantities or a pallet shipment, keeping lines open with technical teams enables us to refine workflows and customize packaging or shipping as needed. In more than one collaboration, program milestones depended on the ability to scale up with identical material to that used for bench discovery—saving time, hassle, and credibility in high-stakes studies. Our long-standing partnerships with major research institutions and biotech firms have benefited from this approach.

    Looking Forward: Continuous Commitment to Quality and Collaboration

    We continue to raise the bar on process control and documentation, influenced as much by regulatory shifts as by the demands of agile research. Even as synthetic chemistry becomes more automated and high-throughput, the fundamentals of good manufacturing stay constant: clean reagents, transparent analytics, and clear communication at every step. User feedback loops remain the primary tool for troubleshooting and continuous process improvement; every complaint is not just addressed but also factored back into training, SOP revisions, and sometimes, raw material supplier reevaluations.

    As research and industrial applications for Imidazo[1,2-a]pyridine, 2-(3-bromophenyl)- continue to expand—from new therapeutic avenues to sophisticated sensor materials—the importance of a reliable, technically sound source grows in tandem. Through deliberate investment in equipment, team expertise, and knowledge-sharing with our user base, we support the missions of teams far beyond our own facility walls. Every batch reflects the lessons learned and passed down from one generation of production chemists to the next, reinforcing the conviction that science, at its most impactful, flows from collaboration and shared standards.