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Ethyl 2-Bromo-3-Chlorobenzoate

    • Product Name Ethyl 2-Bromo-3-Chlorobenzoate
    • Alias Ethyl 2-bromo-3-chlorobenzoate
    • Einecs 261-540-9
    • 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
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    Specifications

    HS Code

    416259

    Product Name Ethyl 2-Bromo-3-Chlorobenzoate
    Cas Number 69418-26-4
    Molecular Formula C9H8BrClO2
    Molecular Weight 263.52 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 344.6°C at 760 mmHg
    Density 1.544 g/cm3
    Refractive Index 1.565
    Purity Typically ≥97%
    Solubility Soluble in organic solvents (e.g., ethanol, dichloromethane)
    Smiles CCOC(=O)C1=C(C(=CC=C1)Cl)Br
    Inchi InChI=1S/C9H8BrClO2/c1-2-13-9(12)7-5-3-4-6(11)8(7)10/h3-5H,2H2,1H3

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

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    Application of Ethyl 2-Bromo-3-Chlorobenzoate

    Applications of Ethyl 2-Bromo-3-Chlorobenzoate in Industrial Manufacturing

    Ethyl 2-Bromo-3-Chlorobenzoate serves as a critical specialty intermediate in diverse industrial synthesis routes, supporting finished goods production in multiple regulated sectors. As a direct manufacturer with active partnerships in fine chemicals, we supply this raw material for multiple value-added transformations. Below we outline specific downstream application scenarios, supported by real usage practices, integration stages, and market-driven compliance requirements.

    1. Pharmaceutical Intermediate Synthesis for Active Pharmaceutical Ingredients (APIs)

    Pharmaceutical manufacturers utilize this compound primarily as a halogenated ester intermediate for the synthesis of targeted APIs, especially within anti-inflammatory and anti-neoplastic research pipelines. The unique substitution pattern on the benzoate ring enables selective reactions in multi-step organic transformations, including halogen exchange and subsequent coupling, which are necessary for achieving high purity and structural specificity in final API molecules. Integration into cGMP-compliant facilities requires strict traceability and analytical validation at each processing step. Downstream sites implement robust in-process controls to ensure consistent incorporation and minimal residual content.

    Industry compliance standards

    • ICH Q7 – Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • Ph. Eur. (European Pharmacopoeia) monograph reference for intermediate control
    • US FDA 21 CFR Part 211 – Current Good Manufacturing Practice for Finished Pharmaceuticals
    • China GMP (2020 Edition) for intermediates and raw materials

    Typical usage ratio

    • 5–20% molar ratio in stepwise synthesis protocols, adjusted according to desired target yield and impurity profile; molarity and equivalents strictly calculated per synthetic route requirements

    Downstream process integration

    • Added during the esterification or halogen substitution stage of multi-step organic synthesis; monitored using LC-MS and NMR throughout reaction and purification phases

    Final product types

    • API intermediates for non-steroidal anti-inflammatory drugs (NSAIDs)
    • Precursors to anti-cancer and anti-microbial chemical entities (under patent development)
    • Specialty pharmaceutical research compounds

    2. Agrochemical Active Ingredient Building Block

    Downstream agrochemical producers adopt this specialty benzoate ester as a halogenated intermediate for targeted synthesis of fungicides and herbicide active ingredients. The well-defined bromine and chlorine functional groups aid in introducing selective efficacy in the parent molecule, optimizing biological activity upon further derivatization. Process engineers involve the material at intermediate coupling or halogen-exchange steps to build robust crop protection actives, ensuring raw material compliance with agricultural safety frameworks.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Annex II (EU) – Requirements for active substance intermediates
    • ISO 9001:2015 Quality Management System in fine chemicals production
    • US EPA 40 CFR Part 158 – Data Requirements for Pesticide Registration

    Typical usage ratio

    • Range: 8–25% by weight in reaction mixtures; actual dose depends on required derivative type and batch scale-up considerations

    Downstream process integration

    • Employed at the stage of ring functionalization and halogen exchange prior to formulation of technical-grade agrochemical actives; involves continuous monitoring of conversion and residuals as per GLP protocols

    Final product types

    • Intermediate compounds for triazole- or strobilurin-based fungicides
    • Precursors to selective herbicidal molecules for cereal and fruit crops
    • Fine chemical intermediates for custom agricultural solution providers

    3. Specialty Dye and Pigment Intermediate

    In the colorants sector, producers of high-performance dyes and pigments incorporate this material as a functionalized benzoate to impart thermal and photostability. The ortho-halogen substitutions create unique platforms for further substitution or azo-coupling, expanding the range of chromophores available to specialty textile and ink formulators. Its reactivity supports batch and continuous processes demanding precise dosing and high reaction efficiency while aligning with manufacturing regulations for restricted aromatic amines and residual halides.

    Industry compliance standards

    • OEKO-TEX® Standard 100 – Safety for textile and leather chemicals
    • EN 71-3:2019 – Safety of Toys: Migration of Certain Elements (for pigment use in children’s products)
    • EU REACH Regulation 1907/2006 Annex XVII – Restrictions on azo dyes
    • ISO 14001:2015 – Environmental Management Systems in chemical plants

    Typical usage ratio

    • 2–10% by weight, with precise adjustment based on target chromophore properties and process scaling; higher ratios reserved for multi-halogenated pigment series

    Downstream process integration

    • Introduced during coupling reactions for azo dye precursors and in the synthesis of halogenated pigment backbones; ratio monitored alongside color intensity and fastness testing protocols

    Final product types

    • High-stability textile disperse dyes
    • Ink pigment intermediates for UV-curable formulations
    • Specialty pigments for plastics and coil coatings

    4. Fine Chemical Intermediate for Advanced Materials

    Manufacturers developing high-purity specialty chemicals for electronics and materials science applications use this compound in process streams where tight halogen control and aromatic substitution are essential. The ability to produce highly pure, structurally defined building blocks enables fabrication of functional materials such as liquid crystal intermediates and performance polymers. Each processing stage requires strict adherence to material compatibility and cross-contamination avoidance, with extended batch records required for QR-traced end-uses.

    Industry compliance standards

    • IPC-4101B – Specification for base materials for printed boards (where chemical intermediates are used in substrate coatings)
    • RoHS Directive 2011/65/EU – Restriction of Hazardous Substances (for electronics chemicals)
    • ISO 9001:2015 and ISO 14644-1 (cleanroom standards for electronics-related fine chemical handling)
    • Japanese Industrial Standards (JIS) for advanced materials supply chain

    Typical usage ratio

    • 0.5–5% by weight, determined by critical design parameters for material function and impurity limits defined by customer QC protocols

    Downstream process integration

    • Blended in during the pre-polymerization phase for specialty polymers, or at the coupling stage for assembling liquid crystal intermediates; process validated for avoidance of halide cross-reactivity and contaminant carryover

    Final product types

    • Liquid crystal material intermediates used in display technology
    • Performance aromatic polymers for electronics and optics markets
    • Functional coatings for microelectronic substrate applications
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    More Introduction

    Ethyl 2-Bromo-3-Chlorobenzoate: An Inside Look at a Key Chemical Building Block

    Product shelves are full of compounds that might not mean much to the average person, but Ethyl 2-Bromo-3-Chlorobenzoate, with its CAS number 90833-47-5, stands out once you dig into the world of fine chemicals. Lab workers, research scientists, and the teams that push new medicines forward have come to know this product for its reliability and unique chemical structure. I’ve found that whenever a molecule needs precise functionalization – where every atom makes a difference to biological activity – the combination of a bromine at the 2-position and a chlorine at the 3-position on the benzoic core gives chemists control that’s hard to match elsewhere.

    Understanding What Makes It Unique

    Ethyl 2-Bromo-3-Chlorobenzoate isn’t just any benzoate ester. With a melting point typically in the mid-40s Celsius and a molecular weight around 263.5 g/mol, its physical appearance as a colorless to pale yellow liquid fits well on a synthetic chemist’s bench. The key difference sits in the precise placement of bromine and chlorine atoms on the aromatic ring. That arrangement doesn’t just make the molecule look interesting on paper; it also dictates how it will behave in cross-coupling reactions and halogen exchange processes.

    Over the years, I’ve noticed that substitutions on a benzene ring are not interchangeable. A bromine, thanks to its larger size and better leaving group character compared to a chlorine, opens doors to Suzuki, Stille, and Heck couplings. With both halogens present, chemists can pick and choose which group to swap out, tuning reactivity in a way that’s simply not possible with benzoates containing just one halogen. The ethyl ester, meanwhile, brings moderate hydrolytic stability and smooths out purification, avoiding some of the stickiness of methyl esters or the stubbornness of bulkier alkyl groups that slow down transesterification.

    Putting It to Work: Applications That Matter

    Researchers don’t pick chemicals at random for complex molecule synthesis. The specialty lies in how certain compounds, like Ethyl 2-Bromo-3-Chlorobenzoate, unlock pathways that traditional precursors don’t. I’ve worked on projects where a team needed a reliable route to generate biaryl units or to introduce a specific building block late in the process. The compound’s ability to undergo site-selective substitution offers freedom during synthetic route development. Medicinal chemists, for example, routinely reach for such molecules in the search for new anti-inflammatory or anticancer agents. The benzoate core shows up in non-steroidal anti-inflammatory drugs and agrochemicals, but it’s the tailored halogenation that opens new possibilities for patentable drug scaffolds or faster lead optimization.

    Traditional benzoates, or those with just one halogen, usually have limited reactivity, forcing chemists into protection-deprotection games or longer synthetic sequences. With 2-bromo and 3-chloro functionality, you can step directly into coupling reactions or plan orthogonal strategies for stepwise modification. This matters a great deal in an industrial setting, where shaving even a single step off a multistep synthesis can mean huge savings in time and waste.

    Model and Specifications: Clarity for Buyers

    Out in the market, the compound mostly appears with assay purities above 98%, often checked by GC or HPLC. You’ll find the model name lining up with its structure, ETHYL-2-BROMO-3-CHLOROBENZOATE, and the molecular formula C9H8BrClO2 captures its essentials. In practice, samples arrive in amber vials or drums, ready to weigh, dissolve, and push forward through reactions. Labs with stringent regulatory requirements look for tight controls on water content, metal impurities, and residual solvents — and suppliers who care about reputation won’t ship products without confirming those details in a batch COA.

    Customization matters, too. Some teams want milligram samples to pilot a reaction; others demand multikilogram lots for scale-up. Producers who understand the needs of research are responsive about packaging and can handle cold-chain shipping or special documentation for regulated industries. The point is, a company that takes E-E-A-T (Expertise, Experience, Authority, and Trustworthiness) seriously makes sure that every lot exactly matches the buyer’s requirements, taking traceability and reproducibility seriously if the customer wants to move seamlessly from R&D to pilot scale.

    How Ethyl 2-Bromo-3-Chlorobenzoate Differs from the Crowd

    I’ve seen plenty of esters and halogenated aromatics in my time, but not all offer the same balance of versatility and selectivity. Derived compounds lacking the second halogen, or with substitutions at the wrong ring position, often show poor yields under cross-coupling conditions or require fiddly workup to separate side products. This molecule’s design allows practitioners to choose which halogen reacts first, keeping synthetic options open.

    Many benzoate esters in the catalog either lack halogens altogether or stick with mono-halogenation. You end up with less control in regioselective reactions or lose performance in late-stage functionalizations. Some alternatives try to blend reactivity by adding activating groups — nitro, trifluoromethyl, or alkoxy — but these sometimes complicate downstream chemistry or introduce safety hazards. Ethyl 2-Bromo-3-Chlorobenzoate stakes out its own place with reliable halogen chemistry without ushering in those complications. In practical terms, if you need a handle to tweak your molecule one atom at a time, this product delivers.

    Why Choosing the Right Supplier Matters

    Anyone who’s handled specialty chemicals for long learns that not all suppliers produce a consistent product. Small differences in starting materials or purification lead to issues later down the line. I’ve run into batches that look fine visually but perform poorly — either the GC shows mysterious peaks, or downstream reactions go off the rails. That’s not just frustrating; it wastes time, materials, and sometimes impacts patent filings if an impurity turns up late in the process. Top suppliers treat their product line as a partnership with the scientific community. They provide robust documentation, keep their records straight, and stand behind every bottle, knowing that reputations in the fine chemicals industry are built year by year.

    GMP compliance, traceable batch records, and transparent analytical data matter a lot, especially for those in regulated industries like pharmaceuticals or agrochemicals. Some of the better companies go an extra step, sharing nitty-gritty details like NMR spectra, GC-MS traces, or even offering samples for confirmation runs. Ethical, experienced producers who value long-term relationships don’t cut corners on purity, documentation, or customer support.

    Staying Safe with Specialty Chemicals

    Working in a lab teaches respect for chemicals, even those with an innocent appearance. The halogenated benzoates present specific safety considerations, both for handling and for long-term workplace hygiene. Ethyl 2-Bromo-3-Chlorobenzoate usually lands somewhere in the middle with respect to risk — not as aggressive as trifluoromethylated compounds, but not something to taste or handle casually. Skin contact or inhalation can bring irritation, so standard safety kit applies: gloves, fume hood, and clear labels to avoid slip-ups.

    Having MSDS documentation on hand becomes more than a formality once you’ve worked through enough incidents. It’s not just about regulations, it’s about keeping lab colleagues safe. Disposal also matters, because local rules on halogenated waste vary between regions and organizations. People who take chemical safety seriously make it part of the onboarding for every new product, not just an afterthought during scale-up.

    Impact on Research and Industry

    A product like Ethyl 2-Bromo-3-Chlorobenzoate rarely finds its way into news headlines, but without this sort of building block, countless breakthroughs would grind to a halt. The pharma sector, for one, depends on accessible and well-characterized intermediates to push projects from discovery to clinical candidates. Patent literature confirms that substitutions on benzene rings drive changes in biological activity, and this ester turns up in structure-activity relationship studies wherever nuanced control over halogenation is needed. Agricultural research, too, makes use of precisely halogenated aromatics to tune activity in herbicides or pest control agents, especially as resistance grows and new modes of action are sought.

    Cost pressures push buyers to seek the best value, but experience has taught me that a cheap, off-spec sample often leads to headaches. Regulatory headaches can mount if a sample deviates from published specs, and wasted man-hours quickly eat up whatever the initial savings looked like. For buyers with a long project horizon and a need for consistent results, it pays to demand proof of expertise from their suppliers.

    Getting the Best from Ethyl 2-Bromo-3-Chlorobenzoate

    Using this compound to its fullest means understanding both the chemistry and the context of your project. In my own work, I’ve see teams make the most out of this molecule by mapping out their reaction sequence in advance, selecting conditions that make the most of the dual halogen pattern. Suzuki couplings, for instance, often start with the bromine, keeping the chlorine ready for another transformation. By planning ahead, chemists avoid dead ends and squeeze more out of every reaction.

    To maintain batch-to-batch consistency, careful recordkeeping helps. Running a quick NMR or GC analysis before embarking on a major synthesis may seem tedious, but it can save an entire run from going sideways. Open lines of communication with suppliers also make a difference – a partner who’s willing to answer technical questions or provide in-depth quality data helps keep projects on track. As chemical supply chains encounter more global uncertainty, reliability and transparency from suppliers become more than just buzzwords; they're a form of risk management built into everyday workflows.

    Sustainability and the Future of Halogenated Benzoates

    As the scientific world looks harder at green chemistry and sustainability, halogenated aromatics like Ethyl 2-Bromo-3-Chlorobenzoate sometimes come under increased scrutiny. Production and downstream use generate waste streams that need careful treatment. The best suppliers don’t just stop at selling the product — they support laboratories in managing waste, handling regulatory filings, and developing safer protocols. I've seen teams work with procurement staff and safety officers to minimize environmental impact, whether it means substituting reagents or improving waste segregation.

    Some new routes aim to make halogenated benzoates with fewer byproducts, turning toward catalytic, solvent-minimized, or atom-economical processes. Synthetic organic chemistry continues to evolve, and the sustainability of specialty reagents will always matter to those with an eye on the future. This means researchers and suppliers have to keep up with both advances in process chemistry and shifts in environmental regulation. Genuine experience shows up in how well a supplier can help navigate these changes, keeping your research compliant and ahead of regulatory demands.

    Potential Solutions to Common Bottlenecks

    Problems never really disappear in chemical synthesis — they just change shape. One frequent headache involves poor reactivity in late-stage functionalization. Here, the advantage of dual halogenation shows itself. By carefully choosing coupling partners and catalysts, chemists have more than one route to reach their target, avoiding the need to backtrack and redesign their approach. Experienced practitioners get the most out of what a product like Ethyl 2-Bromo-3-Chlorobenzoate offers by staying nimble and having backup plans for changing priorities or unexpected results.

    Waste handling also gets easier with planning. Partnering with organizations that recover and recycle halogen-containing waste, or that offer compliant disposal, takes the burden off small labs and makes for a smoother audit process when inspectors come calling. It's worth building these solutions into lab SOPs rather than trusting that disposal will sort itself out at the last minute.

    Supporting Innovation in the Chemical Industry

    In the end, the role of Ethyl 2-Bromo-3-Chlorobenzoate stretches far beyond the reaction flask. As part of the toolkit that drives modern organic synthesis, it supports projects that range from new drug discovery to materials science and agricultural advances. Its blend of reactivity and selectivity, combined with trusted quality from reputable suppliers, makes it a cornerstone for chemists pushing the boundaries of what’s possible. I’ve watched the industry move from batch-by-batch improvisation to a model where traceability and transparency unlock new efficiencies, opening the doors to faster development cycles and higher-value outcomes.

    For anyone looking to take on the challenges of modern synthesis, picking the right building blocks, partners, and processes will always matter. Ethyl 2-Bromo-3-Chlorobenzoate stands as a reliable choice for those who demand both performance and peace of mind. And through its impact on both the bench and the broader industry, it reminds us that real progress in science comes not just from ideas, but from the people and products that turn those ideas into results.