Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

Ethyl 2-Bromo-4-Methyl-1,3-Thiazole-5-Carboxylate

    • Product Name Ethyl 2-Bromo-4-Methyl-1,3-Thiazole-5-Carboxylate
    • Alias Ethyl 2-bromo-4-methylthiazole-5-carboxylate
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    471091

    Chemical Name Ethyl 2-Bromo-4-Methyl-1,3-Thiazole-5-Carboxylate
    Cas Number 134115-07-6
    Molecular Formula C7H8BrNO2S
    Molecular Weight 250.11
    Appearance Light yellow to brownish solid
    Solubility Soluble in organic solvents like DMSO and DMF
    Purity Typically >95%
    Storage Conditions Store at 2-8°C, keep container tightly closed
    Smiles CCOC(=O)C1=NC(Br)=C(C)S1
    Inchi InChI=1S/C7H8BrNO2S/c1-3-11-7(10)5-6(8)9-4(2)12-5/h3H2,1-2H3

    As an accredited Ethyl 2-Bromo-4-Methyl-1,3-Thiazole-5-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing
    Shipping
    Storage
    Application of Ethyl 2-Bromo-4-Methyl-1,3-Thiazole-5-Carboxylate

    Applications of Ethyl 2-Bromo-4-Methyl-1,3-Thiazole-5-Carboxylate in Industrial Manufacturing

    Ethyl 2-Bromo-4-Methyl-1,3-Thiazole-5-Carboxylate plays a key role as an intermediate in specialized segments of industrial manufacturing, providing a targeted building block for downstream synthesis within pharmaceutical, agrochemical, and fine chemical sectors. Our facility supplies this material in bulk volumes directly for integration into regulated processes, serving established product pipelines that rely on defined formulations and compliance protocols.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical companies use our thiazole-based intermediate for the synthesis of select active pharmaceutical ingredients, notably where thiazole cores or bromo-containing heterocycles are essential in the final API structure. Our compound enters multi-step synthesis pathways, reacting with nucleophiles to form key heteroaromatic linkages. Production lines require strict impurity control and documentation for regulatory auditing, with our material purity supporting consistent batch results and downstream validation.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for APIs)
    • USP/NF (United States Pharmacopeia)
    • EU GMP Part II (Active Substances)
    • DMF submission for US FDA reference

    Typical usage ratio

    • 0.25–0.75 molar equivalents per batch, adjusted based on targeted API route and step conversion efficiency

    Downstream process integration

    • Thiazole intermediate enters after initial core assembly, typically in the heterocycle functionalization stage before final API tail modifications

    Final product types

    • Thiazole-based antihypertensive APIs
    • Bromoheterocycle-containing antiviral compounds
    • Specialty antibiotics with thiazole pharmacophores

    2. Agrochemical Synthesis for Fungicide Actives

    Leading crop protection manufacturers incorporate our compound as a precursor in the production of advanced thiazole-based fungicides. The presence of both bromine and ester groups enables downstream chemists to selectively modify the molecule via transesterification, Suzuki coupling, or nucleophilic substitution, forming target active ingredients for use in registered plant protection formulations. Trace contaminant limits and full batch traceability apply throughout agrochemical routes due to regulatory standards.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • OECD GLP (Good Laboratory Practice) for toxicological assessment
    • EU 1107/2009 (Authorization of Plant Protection Products)
    • ISO 9001 certified production batch records

    Typical usage ratio

    • 10–28% w/w of total precursor load per actives batch, depending on target fungicide and required step yield

    Downstream process integration

    • Intermediate introduced during heterocycle extension and halogenation steps, prior to bulk formulation of technical-grade active ingredient

    Final product types

    • Thiazole-based systemic fungicide actives
    • Crop seed treatment agents with enhanced root uptake
    • Leaf-applied fungicide concentrate products

    3. Veterinary Drug Intermediate

    Veterinary drug producers source this thiazole derivative as a required intermediate for synthesizing API candidates for animal health, especially for anti-infective formulations targeting pets and livestock. QC labs audit trace impurity levels and stereochemistry throughout batch runs, as veterinary medicinal compounds observe residue restrictions under veterinary drug regulations across export regions.

    Industry compliance standards

    • VICH GL2 (Good Manufacturing Practice for Active Substances used as Starting Materials)
    • Ph. Eur. (European Pharmacopoeia)
    • Chinese Veterinary Pharmacopoeia for export batches to Asia
    • EC 37/2010 (Veterinary drugs residue control)

    Typical usage ratio

    • Primarily 0.30–0.90 equivalents to reactant in coupling steps, ratio selected per synthetic route and purity requirements

    Downstream process integration

    • Integrated into nucleophilic substitution and ester hydrolysis reactions during penultimate steps before API crystallization

    Final product types

    • Anti-parasitic veterinary actives with heteroaromatic motifs
    • Antibiotic feed additives for monogastric animals
    • Oral suspension veterinary formulations

    4. Fine Chemicals for Specialty Dye Synthesis

    Dye synthesis labs use this compound as a structural core for developing specialty thiazole dyes and brightening agents, exploiting its bromo and carboxyl functionalities for targeted condensation and coupling chemistry. Process engineers ensure tight control of reaction parameters as color properties and product lightfastness rely on precise precursor ratios and impurity profiling.

    Industry compliance standards

    • REACH Annex VII (Registration of Substances in Europe)
    • OEKO-TEX Standard for input chemicals in textiles
    • GMP for Industrial Dyes (EFfCI guidelines)
    • ISO 9001/14001 Quality and Environmental Management Systems

    Typical usage ratio

    • Variable, typically 5–22% w/w in core dye-condensation reaction, based on desired chromophore strength and target batch size

    Downstream process integration

    • Introduced during azo or thiazole chromophore condensation step, immediately prior to sulfonation and salt formation for final dye product

    Final product types

    • Thiazole-reactive textile dyes
    • Fluorescent brightening agents for paper and plastics
    • Color-fast PU coating additives

    5. Electronic Chemical Intermediate for Organic Semiconductors

    Manufacturers in the electronics sector utilize this thiazole ester to synthesize advanced organic molecules for organic semiconductors and OLED precursors. The bromo substitution facilitates further cross-coupling reactions, notably in C-H activation and Stille/Suzuki-Miyaura couplings, allowing for fine-tuned control of electronic and optical properties critical for device applications.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances Directive)
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals)
    • IEC 62474 (Material Declaration for Electrical Products)
    • UL 94 (Flammability Rating for Plastics Materials)

    Typical usage ratio

    • Range of 3–17 mole% in batch synthesis of intermediate layers, precise ratio selected per target functional group density and device architecture

    Downstream process integration

    • Enters small molecule and polymer synthesis routes for hole-transport and electron-blocking layers, introduced at aromatic coupling or condensation stages

    Final product types

    • OLED emitter precursors
    • Organic photodetector functional materials
    • Thin film transistors for display panels
    Free Quote

    Competitive Ethyl 2-Bromo-4-Methyl-1,3-Thiazole-5-Carboxylate prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

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

    Certification & Compliance
    More Introduction

    Exploring Ethyl 2-Bromo-4-Methyl-1,3-Thiazole-5-Carboxylate: A Trusted Intermediate in Modern Synthesis

    A Close Look at Ethyl 2-Bromo-4-Methyl-1,3-Thiazole-5-Carboxylate

    Chemistry rarely stands still, especially in the search for sharper tools and smarter building blocks. Ethyl 2-Bromo-4-Methyl-1,3-Thiazole-5-Carboxylate has carved out a real role in laboratories and industries rooted in fine chemicals and complex pharmaceutical synthesis. I remember the first time I watched a colleague weigh out this precise compound—the deep trust she had in its consistency, the intention behind her workbench prep, and the silent promise of reliable results. This specialty molecule serves more than one purpose. Researchers and development teams keep turning to it, not just for what it is, but for what it does, and the way it keeps showing up to solve demanding synthetic challenges.

    Breaking Down the Model and Key Specifications

    Chemical suppliers list this compound by its technical name, but real work with it confirms why it attracts attention: a thiazole ring functionalized with both a bromine and a carboxylate ester. The formula speaks for itself: C7H6BrNO2S. The bromine atom, locked on the thiazole ring at position 2, introduces useful reactivity when it comes to coupling reactions and targeted modifications. The methyl group at position 4 brings just enough electron-donating influence to help with selectivity—it's not just decorating the ring, it nudges reactions down a more predictable path. The ethyl ester, dangling from the carboxylate at position 5, serves as more than a handle for purification; it primes the molecule for more selective hydrolysis or amidation, which often streamlines downstream chemistry.

    I’ve seen specifications vary slightly across suppliers, but quality control never feels like a side issue. Purity often sits north of 97%, backed by chromatographic analysis or NMR to check for key contaminants. Moisture content matters too, since hydrolysis can threaten stability over time. Technical teams don’t just take these numbers for granted—they chase them, batch after batch, since one impure load can sideline weeks of effort. Packaging, whether in smaller glass vials for research or in industrial drums for production runs, invariably leans on air-tight seals and careful labeling. These practical details may sound dry, but they end up saving real money and helping avoid mysterious reaction failures down the line.

    How Ethyl 2-Bromo-4-Methyl-1,3-Thiazole-5-Carboxylate Finds Its Calling

    Applications, not specs, bring a molecule to life. Chemists often reach for this bromo-methyl thiazole ester as a keyed-in intermediate, not a final stop. The presence of the bromine atom means you can form carbon-carbon bonds in a controlled way, especially during Suzuki or Stille couplings. There’s a reason these reactions sit at the core of many medicinal chemistry campaigns; they save steps, cut down by-products, and yield libraries of analogues without starting from scratch every time.

    My own run-ins with this compound have come through collaborative projects where the goal is new lead structures for anti-infectives or anti-inflammatories. Teams rush to create small-molecule libraries, each with subtle tweaks to this essential core. The thiazole ring itself isn't just a pretty scaffold—rich literature points to its presence in pharmaceuticals, agrochemicals, and even dyes. Conjugating new groups at one end while tuning ester reactivity at the other unlocks all sorts of structure-activity relationships you’d never dream up from a textbook alone.

    Beyond drug discovery, this esterified, brominated thiazole anchors itself in custom synthesis for research tools and specialty reagents. Several biotech firms now rely on similar scaffolds to generate tailored probes used in imaging or diagnostics, betting on thiazole's properties to site-specifically label proteins or modulate enzyme function. A typical chemist, facing a complex target, chooses this intermediate because it cuts through synthetic hurdles and reduces development cycles, often making the difference between a stalled project and a promising one.

    Comparison With Other Building Blocks

    With chemical building blocks, choice rarely feels arbitrary. Each feature of this molecule has a job. Comparing Ethyl 2-Bromo-4-Methyl-1,3-Thiazole-5-Carboxylate to its cousins reveals what’s unique. Many labs use similar thiazole derivatives—sometimes a plain methylthiazole, other times a non-brominated version, or switches to a methyl ester instead of ethyl. Features like ester chain length or halogen substitution sound subtle on a supplier’s page, but real-world outcomes diverge. A methyl ester might show slightly less stability under certain reaction conditions, or it might hydrolyze too fast for a given need. Swapping bromine for iodine may change reactivity but spikes cost or lowers availability.

    You notice these differences only after hours spent troubleshooting a sluggish coupling or tracing down where an unexpected impurity creeps in. Quality matters most when scale goes up. A good batch of Ethyl 2-Bromo-4-Methyl-1,3-Thiazole-5-Carboxylate delivers predictable coupling yields, smooth hydrolysis, and less by-product—a tighter window of error that makes or breaks late-stage projects. While other thiazole esters can, technically, supplement for certain steps, the precise placement of bromine and the ethyl ester mark this one out for its balance of reactivity and stability. In short, it’s not just functional; it’s adaptable.

    Reliability and Reproducibility—Why They Matter

    In chemistry, trust in a reagent often comes from hard-won experience. Tackling multi-step syntheses means betting that every building block will behave the same way every time. Labs might switch suppliers, but no one takes supply chain reliability for granted—missing or mischaracterized intermediates have sunk major programs before. In crowded fields like medicinal chemistry, tight deadlines and budgets punish anything less than dependable performance.

    Repeated success with this thiazole ester links directly to robust test data, experienced distribution networks, and a willingness by suppliers to openly share specification sheets and analytical data. The industry grows more demanding every year; companies want not just to save cost per gram but to shave week-long delays caused by failed reactions or product recalls. Third-party analytics—HPLC reports, proton and carbon NMR, even mass spectrometry—form part of the product’s identity, not an afterthought. My former lab mates swapped horror stories about poorly characterized lots that tanked yields or, worse, introduced sneaky impurities only detected by eagle-eyed analytical chemists months after launch. A consistently pure supply minimizes these risks.

    Supply Chain, Storage, and Handling: Real-World Details

    This compound isn’t particularly difficult to store, but small missteps add up. Extended exposure to air or moisture nudges the ester toward unwanted breakdown. Most researchers I know stash it in tightly sealed amber bottles, often in dedicated refrigerators to guard against temperature swings. Transport protocols matter, especially for larger operations. Careful packaging avoids cross-contamination or spillage, which keeps both quality and safety standards high.

    Some may shrug at these logistics, but lost product and wasted time often stem from neglected storage guidelines. Chemical stability studies provide reassurance that the compound, if left undisturbed away from direct sunlight and strong acids or bases, retains its sharp performance profile month after month. That dependability translates all the way into the data my colleagues and I depend on for regulatory filings, academic publications, and patent submissions.

    Ethical Sourcing and Environmental Impact—A Long View

    I’ve watched the chemical market shift in real-time toward more transparent, responsible sourcing. Regulatory pressure aside, researchers and companies increasingly ask tough questions about how their reagents are made and shipped. This thiazole ester, with its bromine atom and organic synthesis background, presents risks if produced in poorly managed facilities. Top suppliers publish more about their raw material traceability, waste handling, and ongoing efforts to limit emissions. Buyers don’t just want purity anymore; they want proof their purchase won’t haunt their compliance logs years later.

    Beyond paperwork, greener chemistry initiatives now encourage the use of reagents that avoid or minimize toxic by-products. Some labs seek thiazole intermediates crafted with safer solvents and renewable feedstocks, even when cost hovers a bit higher. Over time, this preference hasn’t only improved public perception; it’s also tightened margins and pushed suppliers to invest in better purification technology and waste recycling—making the best products also the most ethically sound.

    Innovation and Access: Why This Building Block Still Matters

    Athletes of chemistry do more than just repeat old moves. They push limits, often blending intuition honed on the benchtop with technical breakthroughs from across the globe. Ethyl 2-Bromo-4-Methyl-1,3-Thiazole-5-Carboxylate might not make explosive headlines, but it forms the backbone of countless exploratory projects. Advanced synthesis groups have leveraged slight tweaks to the ester or ring system to open doors no one saw even a few years ago. As patents expire and new diseases demand fresh treatments, the versatility of this specific intermediate unlocks options—producing molecules that shape future therapies and research tools in ways other, less tuned, reagents can’t match.

    Innovation doesn’t always sprout from the most glamorous sources. More often, it comes from perfecting basics until they work under the toughest conditions. Ethyl 2-Bromo-4-Methyl-1,3-Thiazole-5-Carboxylate has stuck because it outperforms similar thiazoles with less fiddling, reducing rework and helping scale pilot reactions to commercial processes. Even academic researchers—those working under tight grants and steep journal requirements—know they’re more likely to succeed when starting with a well-characterized, consistent intermediate.

    Research Challenges and the Path Forward

    No chemical is perfect. Even the most respected intermediates show limitations. Some users have flagged occasional issues with limited solubility in non-polar solvents, or the need for extra steps to achieve ultra-pure material for sensitive biological work. But these challenges rarely stall progress outright. What matters most is open, clear communication between suppliers and users, making sure each new lot comes with the right documentation and that buyers aren’t left guessing about reactivity quirks or hidden incompatibilities.

    I’ve often traded stories with peers about optimizing the use of this reactivity—sometimes by tweaking solvent conditions, other times by fine-tuning reaction temperature or stoichiometry. The feedback loop between bench chemists and suppliers fuels real improvements, whether in packaging improvements or purification upgrades. As more teams share what works and what falls short, the overall quality and value of the product continues to rise, benefiting everyone along the pipeline—from research associate to final patient or customer.

    Cost Considerations and Maximizing Value

    Budgets fill every conversation in modern labs. Pricing on Ethyl 2-Bromo-4-Methyl-1,3-Thiazole-5-Carboxylate has settled into a competitive range—as expected for a mid-level specialty intermediate not tied to rare feedstocks or exotic manufacturing routes. Bulk buying provides healthy discounts, but savvy teams know that skimping on quality for a few dollars per gram rarely pays off. Opportunities to economize come from smarter planning and accurate forecasting, not gambling on unproven sources or skipping needed analytics.

    Buying high-grade intermediates in bulk requires trust—not just in the molecule, but in the partner. Best practice leans toward qualified suppliers with strong logistics, custom lot reservation, and robust after-sales support. Mistakes in chemical buying sometimes only reveal themselves months later, often during scale-up or regulatory inspection. Investing in strong partnerships up front—even if every molecule looks the same on paper—guards against those costly surprises.

    Potential Solutions to Limitations and Industry Needs

    Improvements always seem possible. End-users would benefit from more granular characterization for each batch, with streamlined access to certificates of analysis and up-to-date safety guidance. In my experience, better supplier communication prevents confusion—and supports researchers when issues arise. Automated lot tracking and digital certificate sharing can cut administrative lag and bolster supply traceability, supporting both compliance and user confidence.

    Industries hungry for low-impact, high-performance intermediates keep pushing for greener solvents, energy-efficient synthesis, and packaging options built for both safety and sustainability. Ongoing collaboration between users and vendors can advance low-waste, closed-loop manufacturing, reducing risk and improving market reputation. Stronger partnerships between chemical producers, academic labs, and pharma developers make it easier to iterate at every stage, from bench to batch scale, cutting down waste and keeping only the best material in play.

    Why Experience Matters—Personal Reflections

    Working with Ethyl 2-Bromo-4-Methyl-1,3-Thiazole-5-Carboxylate has taught me that the best results in chemistry come from a blend of technical rigor and lived experience. Every reliable reaction outcome builds on a foundation of unwavering product quality, transparent supplier relationships, and the willingness to troubleshoot and improve with each use. The compound’s enduring presence across diverse chemical domains isn’t just a result of clever design on a chalkboard; it’s the sum of trust, effort, and persistent trial and error in the world’s labs.

    This compound, like many unsung heroes of synthesis, tells a story not just of atoms and bonds but of people—experimenters, analysts, and buyers—invested in moving science forward. They depend on this intermediate to behave as expected and adapt to unpredictable challenges. As research grows more demanding and timelines shrink, products that marry versatility with reliability help carry the load. That’s true value—delivered not in abstract promises, but in results that matter day after day.

    Looking Ahead

    Demand for specialized chemical intermediates only accelerates. Ethyl 2-Bromo-4-Methyl-1,3-Thiazole-5-Carboxylate, through years of steady performance and constant refinement, stands as a testament to how practical chemistry evolves. New users come for the technical perks; they stay for the certainty that the molecule won’t let their projects down. In a crowded market where some compounds are forgotten as soon as they’re replaced, this one has earned its place—not through hype, but through results only true experience can deliver.