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5-Chloro-2-Methoxyphenylboronic Acid

    • Product Name 5-Chloro-2-Methoxyphenylboronic Acid
    • Alias 5-Chloro-2-methoxybenzeneboronic acid
    • Einecs 418-020-5
    • 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

    985154

    Product Name 5-Chloro-2-Methoxyphenylboronic Acid
    Cas Number 365543-42-4
    Molecular Formula C7H8BClO3
    Molecular Weight 186.40 g/mol
    Appearance White to off-white solid
    Melting Point 152-156 °C
    Purity Typically ≥97%
    Solubility Soluble in DMSO, slightly soluble in water
    Storage Temperature 2-8°C (refrigerated)
    Smiles B(C1=CC(OC)=C(C=C1)Cl)(O)O
    Inchi InChI=1S/C7H8BClO3/c1-12-7-3-2-5(9)4-6(7)8(10)11/h2-4,10-11H,1H3

    As an accredited 5-Chloro-2-Methoxyphenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "5-Chloro-2-Methoxyphenylboronic Acid, 5g," with CAS number, purity, and hazard warnings displayed.
    Shipping 5-Chloro-2-Methoxyphenylboronic Acid is shipped in tightly sealed containers to protect from moisture and air. It is typically packed in compliance with chemical safety regulations, labeled appropriately, and transported at ambient temperature. Shipping may be subject to regulations for hazardous chemicals, so check local and international guidelines before ordering or transporting.
    Storage 5-Chloro-2-Methoxyphenylboronic Acid should be stored in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizing agents and acids. It is advisable to store the chemical under an inert atmosphere, like nitrogen, to prevent degradation and preserve its stability.
    Application of 5-Chloro-2-Methoxyphenylboronic Acid

    Applications of 5-Chloro-2-Methoxyphenylboronic Acid in Industrial Manufacturing

    5-Chloro-2-methoxyphenylboronic acid is a specialized boronic acid derivative used across several segments in chemical synthesis and advanced material development. As a direct manufacturer, we supply this intermediate for integration in regulated pharmaceutical, agrochemical, electronics, and specialty polymer fields. Below we detail downstream scenarios with tailored compliance, usage, process, and finished product guidance.

    1. Pharmaceutical Intermediate Synthesis

    Downstream pharmaceutical manufacturers employ 5-chloro-2-methoxyphenylboronic acid as a key building block in Suzuki-Miyaura cross-coupling reactions. This intermediate enables the construction of complex biaryl structures essential in the synthesis of targeted small molecule therapeutics. Formulation chemists select its reactivity for the assembly of APIs requiring chloro- and methoxy-functionalized phenyl rings, ensuring efficient yields and process repeatability during multi-step syntheses of antineoplastic and anti-infective drug candidates.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF requirements for drug substance manufacturing
    • European Pharmacopoeia (Ph. Eur.) monographs where applicable
    • 21 CFR Parts 210/211 cGMP for Finished Pharmaceuticals

    Typical usage ratio

    • Applied at a 1.0–1.2 molar equivalent excess relative to halogenated substrate in Suzuki coupling; ratio optimized based on the required reaction scale and stoichiometry in API route design

    Downstream process integration

    • Charged during initial stages of Suzuki or related palladium-catalyzed couplings for API core structure assembly in reactors with temperature and atmosphere control systems

    Final product types

    • Anticancer agents containing biaryl motifs
    • Fluoroquinolone antibiotic intermediates
    • Central nervous system drug precursors
    • Pharmaceutical reference standards

    2. Agrochemical Active Ingredient Development

    Producers in the crop protection sector utilize this boronic acid in the synthesis of agrochemical actives, especially those relying on aryl-substituted scaffolds. The material's functional groups support selective coupling steps, allowing for the creation of advanced herbicides and insecticide intermediates displaying high field stability and plant compatibility. Its integration ensures precision during scale-up and impurity control to safeguard downstream formulation quality.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 for chemical process manufacturing
    • REACH (EC 1907/2006) compliance for European distribution
    • OECD Guidelines for Testing of Chemicals

    Typical usage ratio

    • Employed typically in 1.1–1.5 molar ratio versus halogenated partner in batch synthesis; ratio determined by desired conversion and minimization of by-product formation

    Downstream process integration

    • Added during key aryl-coupling steps within the multi-stage synthesis of active ingredient cores, preceding downstream formulation and encapsulation

    Final product types

    • Selective herbicide active ingredient intermediates
    • Broad-spectrum insecticide synthons
    • Fungicide precursor compounds
    • Pesticide technical grade actives

    3. Organic Light-Emitting Diode (OLED) Material Synthesis

    Advanced electronics manufacturers integrate this compound as an aryl source for the synthesis of conjugated organic materials in OLED display and lighting fabrication. Its structural attributes support the fine-tuning of emission wavelengths and charge transport in organic semiconductors, contributing to consistent thin-film performance for next-generation electronic display panels and lighting solutions. Precise process and purity control are essential for downstream device reliability.

    Industry compliance standards

    • RoHS Directive (EU 2011/65) for hazardous substance restrictions
    • IEC 61249-2-21 Halogen Free Material standards
    • ISO 14001:2015 for environmental management in material production
    • Internal QC protocols for trace-level metal and halide residues in electronic raw materials

    Typical usage ratio

    • Used in 1.0 equivalent relative to the aryl halide coupling partner; adjusted by material scientist for batch scale and electronic performance targets

    Downstream process integration

    • Charged during the synthesis of emitter or transport layer precursors; post-reaction, the material is purified and processed for polymerization or solution casting

    Final product types

    • Small molecule OLED emitters
    • Conductive polymer intermediates
    • Precursors for display-grade organic semiconductors
    • Thin-film organic lighting materials

    4. Specialty Polymer Modification

    Producers in the specialty polymer industry exploit this boronic acid derivative to introduce functionalized aromatic units into polymer matrices via post-polymerization modification pathways. The methoxy and chloro substituents impart unique polarity and compatibility with engineering polymers, influencing thermal and mechanical performance for advanced coatings, adhesives, and engineered composite components. Controlled grafting and copolymerization protocols determine final product consistency and application suitability.

    Industry compliance standards

    • ISO 9001-certified polymer manufacturing and process control
    • FDA 21 CFR 177.1520 for indirect food contact (where applicable)
    • ASTM D256 for polymer mechanical performance
    • REACH pre-registration for modified polymer constituents in the EU

    Typical usage ratio

    • Incorporated at 0.5–2% w/w relative to total monomer or polymer backbone in post-modification; ratio adjusted based on required end-use functionality and mechanical property targets

    Downstream process integration

    • Employed in graft-copolymerization or chain-end functionalization after initial polymer synthesis; incorporated via solution or melt-phase blending using controlled addition and reaction monitoring

    Final product types

    • High-performance coating resins
    • Engineering thermoplastics with custom aromatic functionalities
    • Adhesive formulation additives and binders
    • Advanced composite resin systems
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    Certification & Compliance
    More Introduction

    5-Chloro-2-Methoxyphenylboronic Acid: Deep Value for Synthesis and Research

    The Shifting Role of Boronic Acids in Modern Chemistry

    Anyone who’s been around chemical synthesis for long knows the persistent demand for clean, functional, and dependable boronic acids. Our team has watched this class of compounds cement its place in all sorts of reactions. From pharmaceutical labs optimizing targets to material scientists shaping electronic polymers, the wide reach of boronic acids stands out. Each variation brings its own quirks and skills, and 5-Chloro-2-Methoxyphenylboronic Acid has stepped up in ways that keep many research and manufacturing channels humming efficiently.

    Meet 5-Chloro-2-Methoxyphenylboronic Acid: Structure with Purpose

    In the lab, little details shape the course of a synthesis. Here, the molecular structure of 5-Chloro-2-Methoxyphenylboronic Acid makes it a regular visitor to our benches. The combination of chloro and methoxy functional groups leads to more than just another addition to the boronic acid catalog. The chloro group holds its own against many conditions, offering resilience and specific reactivity. The methoxy group, on the other hand, changes the electronic properties of the aromatic ring and gives this compound a versatility that can sway both the direction and outcome of Suzuki–Miyaura coupling reactions, among others.

    Too often, chemists get stuck patching systems with generic building blocks. Out in the field, we’ve tackled these same challenges: unpredictable yields, off-target reactivity, and frustrating purification routines. Each time, selecting the right starting material trimmed down wasted time and money. Among the choices on the shelf, 5-Chloro-2-Methoxyphenylboronic Acid consistently brings clarity to synthetic problems: less byproduct junk, more straightforward isolation, and solid performance under scalable conditions.

    A Manufacturer’s Lens: From Sourcing to Scale-Up

    Making this compound on a steady, reliable schedule isn’t as easy as tossing reagents together and crossing fingers. We’ve spent years narrowing the window between stability and reactivity, because it’s the edge that makes or breaks performance downstream. Even the temperature and humidity control during crystallization shape the final workup: with boronic acids, those tweaks prevent oxidative degradation and keep purity levels strong batch after batch.

    Each kilogram we release into the world reflects a tug-of-war between cost, safety, and reproducibility. With 5-Chloro-2-Methoxyphenylboronic Acid, purity levels at or above 98% (with consistent HPLC profiles) have pushed our partners’ results to more predictable spaces. Run-to-run reproducibility matters: one missed impurity, one slip in moisture content, and the whole forward synthesis can spiral, wasting valuable material and labor.

    Why 5-Chloro-2-Methoxyphenylboronic Acid Stands Out

    Comparisons with other boronic acids pop up routinely in meetings with clients and partners. It’s only fair—tons of lookalike molecules fill the catalogs. The distinction for this specific compound grows clear once people look past the basic specifications and see how it handles real-world chemistry.

    Compounds bearing an extra methyl group or missing the chloro function might look attractive at first, but final reaction profiles tell a different story. Meticulous characterization demonstrates that 5-Chloro-2-Methoxyphenylboronic Acid delivers a tighter range of side products in cross-coupling reactions. The methoxy substituent gives just the right balance—enough electron donation to activate the aromatic ring, but not so much as to destabilize the system. Particularly in Suzuki couplings where electronic tuning dramatically sways product outcome, we’ve watched it outperform analogs time and again, both in reaction scope and selectivity.

    One of the lessons from handling boringly similar molecules: every tiny change in the aromatic system impacts whether a chemist spends a night in the lab or gets home for dinner. For 5-Chloro-2-Methoxyphenylboronic Acid, we’ve seen improved yields, increased substrate compatibility, and simpler purification versus rows of less tailored starting materials. It isn’t magic. It’s incremental trust earned from hundreds of runs and partnerships with process chemists who test every claim with industrial scale-ups.

    Practical Results in Pharmaceutical and Materials Chemistry

    Demand in pharmaceuticals is easy to understand. What the world often overlooks is how small changes in boronic acids translate into massive gains for medicinal chemists. We’ve supplied our product to projects chasing kinase inhibitors, dopamine analogs, and a range of anti-infectives. Here, the subtle electron effect induced by chloro and methoxy groups enables selective bond formation, especially when every atom counts in late-stage functionalization or fragment-based design.

    In our experience, generic phenylboronic acid fails more times than it succeeds in advanced, heteroaryl cross-couplings. Materials science, especially for OLED and organic polymer research, tells a similar story. Connectivity, color tuning, and charge properties all react sharply to small tweaks in the aromatic building blocks. Our partners in the electronics sector have chosen this compound for improved performance in conductive polymers. They’ve shared results where injection-molded devices display sharper emission spectra and more stable device lifetimes, all starting from carefully built monomers leveraging the specific structure of the phenylboronic acid we produce.

    The Human Factor: Scale, Safety, and Process Tolerance

    Our work often starts with concept meetings—chemists mapping out retrosynthetic routes with markers on whiteboards. The reality of taking a reaction from milligram scale in a university lab to multi-kilogram runs for industry plants brings technical hurdles. The stability, solubility, and safe handling profile of 5-Chloro-2-Methoxyphenylboronic Acid added flexibility for every stage, from pilot projects up through kilo lots.

    Solubility in common organic solvents—THF, toluene, dioxane—means the compound drops seamlessly into most operational flows. We’ve tuned the crystal form to minimize caking during shipping and storage. Handling this compound requires no exotic hazard protocols, as long as normal organic synthesis hygiene is followed. With shelf-stable packaging, we’ve removed a common frustration for users who want to avoid repeat testing or reworking old stock after a humid summer.

    It’s easy to overlook safety until something goes wrong—a leaky drum or an incompatible secondary containment can reset progress overnight. Through batch testing and close attention to impurity profiles, we’ve kept heavy metal content and trace halide impurities well below the thresholds set by industry standards. The end result is a smoother regulatory review for downstream products.

    Building on Feedback: Improving Every Run

    We don’t print new brochures every month advertising improvements. Instead, we listen to the researchers who hit roadblocks. Analytical teams at pharmaceutical and materials companies often surface challenges that textbooks didn’t predict—trace degradation pathways, sensitive byproducts, sudden color changes on standing. Our work as the manufacturer means we own those results and learn from every complaint or glowing report.

    With 5-Chloro-2-Methoxyphenylboronic Acid, direct conversations with end users led to tweaks in granulation (reducing dust, improving pourability) and packaging changes that made cold-chain storage unnecessary for many climates. Where clients flagged issues with moisture-induced aggregation or slow dissolution in polar solvents, we changed drying techniques and particle size filtering procedures. These adjustments delivered measurable gains in ease of use and final yields at customer sites without heavy additional cost.

    Quality isn’t something that comes from a certificate alone. It’s a direct result of care and vigilance in production—things you can’t delegate to a third party. We run every batch through our own HPLC and NMR routines, cross-checking for isomeric purity and breakdown patterns. This investment pays off as peers upstream and downstream avoid unpredictable snags and delays once the material hits their benches.

    The Craft of Manufacturing—Beyond Catalog Numbers

    Many customers first contact us because they tired of unexplained failures with materials from traders or faceless catalog houses. As the manufacturer, we focus on reproducibility over mass marketing. Our jobs depend on earning the trust of chemists who stake career-defining runs on the starting material they receive. The difference shows up in fewer rejected lots, higher conversion rates, and less downtime for plant techs who need to keep timelines on track.

    We look beyond simple price competition—anyone can dump tonnage onto the market and hope something sticks. Instead, process experience creates a buffer against cascading problems. Our field teams share production schedules and documentation with users so they understand the backgrounds and can adjust for tight program deadlines. Rigorous audits on incoming raw materials and continuous training ensure that each output matches the last, regardless of order size or destination.

    Why Not Settle for Generic Boronic Acids?

    Generic compounds tempt with low prices and rapid shipment, but the real cost builds with inconsistency and uncertainty. We watched some clients chase savings by substituting lower-spec material, only to lose weeks troubleshooting strange NMR peaks or flakey conversion rates. With 5-Chloro-2-Methoxyphenylboronic Acid, the difference jumps off the page—cleaner reactions, reduced batch-to-batch variation, and dependable metrics every time.

    We remember one customer trying unsuccessfully to scale a key Suzuki coupling for a late-stage pharmaceutical intermediate. Generic boronic acid routinely yielded inconsistent transfer hydrogenolysis results, adding cost and risk to a critical project milestone. After switching to our product and adjusting only minor variables, the route stabilized, and failed reactions dropped almost to zero. This isn’t an isolated case—it repeats in settings from pilot-scale tablets to kilogram-scale materials chemistry syntheses.

    Continued Improvements—What’s on Our Bench Now

    Industry needs continue to evolve. New reaction conditions, greener solvent systems, and more demanding regulatory expectations shape how we approach 5-Chloro-2-Methoxyphenylboronic Acid and all our core outputs. We’re pushing toward more sustainable production routes, investing in reagent recovery and energy-efficient crystallization, and scaling green chemistry programs tightly tied to market feedback.

    For large-scale partners, we’ve started to develop custom intermediates where a similar substitution on the aromatic nucleus shifts properties for niche downstream uses. Sharing data from batch stability studies across multiple climates, we’re responding to customer requests for more granular impurity profiles and even cleaner baseline spectra. Some collaborators want above-99% purity or tailored particle sizes, and our process designers are bringing those requests into active workflow—always balancing the technical tradeoffs at hand.

    Every change—tweaking the drying curve, adjusting crystallization time, evaluating alternate solvents—gets measured against our experience keeping processes safe and scalable. Through honest dialogue with research and production chemists across the world, we sharpen each aspect of our manufacturing routines to serve a range of disciplines: pharma, agrochemical, fine chemicals, and the rapidly changing space of printable electronics.

    Ownership, Commitment, and Accountability

    As manufacturers, we answer every question about our process, batch records, and analytical reports. We shoulder the responsibility for what arrives in a customer’s plant—no excuses, no backpedaling with blame on mysterious vendors or brokers. From the head chemist who signs off each release to the line technicians packing up finished product, everyone here knows their work ends up under the microscope at research sites, production lines, and third-party audits.

    Open communication keeps relationships with clients strong. We share documentation ahead of shipments, plan logistics to avoid customs hangups and weather delays, and stay available for troubleshooting—even if the synthesis result points back to an unlikely source of impurity downstream. This approach fosters smarter partnerships: chemists tell us when something’s wrong, and we learn together, preventing the same issues on future orders.

    At the scale of industrial chemistry, no single product holds all the answers. Still, reliable, high-performing materials like 5-Chloro-2-Methoxyphenylboronic Acid give researchers and manufacturers the confidence to map out long development cycles without guessing at every step. This mindset pushes us to do better—not just for one cycle, but across the evolving landscape of synthetic science.

    In Summary: The Manufacturer’s Promise

    Each batch of 5-Chloro-2-Methoxyphenylboronic Acid represents years of expertise and adaptation, not just stock in a warehouse. Every improvement comes from listening to the community and rigorously scrutinizing outcomes. Whether the destination lies in early-stage drug discovery, final active ingredients, or cutting-edge materials science, we back each shipment with process transparency and personal accountability. These principles drive every kilogram produced and shape the reputation we stand behind in the market.

    We welcome feedback, collaboration, and challenge—that’s how chemistry moves forward. With 5-Chloro-2-Methoxyphenylboronic Acid and the team standing behind it, your work gains a partner defined by reliability, honesty, and the drive to push above just “good enough.”