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3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carbonyl Chloride

    • Product Name 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carbonyl Chloride
    • Alias CMIC
    • Einecs 416-560-1
    • 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

    694368

    Chemical Name 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carbonyl Chloride
    Molecular Formula C11H7Cl2NO2
    Molecular Weight 256.09 g/mol
    Cas Number 31576-27-1
    Appearance White to off-white solid
    Purity Typically >98%
    Solubility Soluble in common organic solvents (e.g., dichloromethane, acetone)
    Storage Conditions Store in a cool, dry place; keep container tightly closed
    Reactivity Reacts with water, alcohols, and amines
    Smiles CC1=CC(=NO1)C2=CC=CC=C2ClC(=O)Cl

    As an accredited 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carbonyl Chloride 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 “3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carbonyl Chloride, 10 grams,” tightly sealed, with hazardous warning symbols.
    Shipping The chemical **3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carbonyl Chloride** is shipped in tightly sealed, corrosion-resistant containers, typically under inert atmosphere. It is packaged and labeled according to hazardous material regulations, protected from moisture and direct sunlight, and transported at ambient temperature, in compliance with relevant local, national, and international shipping guidelines.
    Storage Store 3-(2-Chlorophenyl)-5-methylisoxazole-4-carbonyl chloride in a cool, dry, well-ventilated area away from moisture and incompatible substances such as bases and strong oxidizers. Keep the container tightly closed under an inert atmosphere, such as nitrogen or argon. Protect from light and store at temperatures recommended by the manufacturer, typically at 2–8 °C. Handle with appropriate personal protective equipment.
    Application of 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carbonyl Chloride

    Applications of 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carbonyl Chloride in Industrial Manufacturing

    As an established chemical manufacturer, we focus on supplying high-purity 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carbonyl Chloride for advanced chemical synthesis. This intermediate’s unique structure and reactivity profile support specialized downstream production in pharmaceutical, agrochemical, and fine chemical industries. Below, we detail its real-world industrial integration, based on end-user formulation, regulatory compliance, and practical downstream processing.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    Research-driven pharmaceutical companies select this compound for constructing targeted isoxazole motifs within novel drug molecules, especially CNS-active agents and anti-inflammatory APIs. Its acyl chloride group ensures selective acylation reactions, facilitating the timely build-up of core frameworks critical to API activity and patent protection. Stringent regulatory oversight and validation steps dictate the QA protocols and supply chain transparency in this sector.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU Regulation 2016/161 for APIs traceability
    • USP and Ph. Eur. monographs for relevant intermediates
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • Stoichiometric addition in acylation step: 0.9–1.1 molar equivalents per targeted amine or alcohol group, adjusted based on impurity profile and scale-up parameters.

    Downstream process integration

    • Intermediate introduction occurs after initial ring formation, via direct solvent-phase coupling; downstream purification includes solvent exchange and crystallization before API key-step conversion.

    Final product types

    • CNS-active small molecule drugs
    • Anti-inflammatory pharmaceutical APIs
    • Isoxazole-based experimental compounds for clinical trial batches

    2. Agrochemical Herbicide Intermediate Synthesis

    Major agrochemical manufacturers utilize this material in the synthesis of modern heterocyclic herbicide actives, where it acts as a building block for constructing isoxazole derivatives with high selectivity against weed species. It undergoes nucleophilic substitution or coupling reactions under controlled conditions, with production following strict environmental and worker safety protocols. Quality demands in this application include consistently low side-product profiles and traceability to support downstream registration dossiers.

    Industry compliance standards

    • ISO 9001:2015 for chemical production management systems
    • Regulation (EC) No 1107/2009 on plant protection products
    • FIFRA (USA) registration support data integrity
    • REACH Annex II chemical safety and hazard communication

    Typical usage ratio

    • Reactant charge in coupling stages: 1.0–1.3 equivalents based on downstream crop selectivity screens and target impurity cut-off.

    Downstream process integration

    • Fed into anhydrous solvent phase with heterocycle precursors; intermediates undergo work-up procedures including aqueous wash and silica plug filtration before subsequent formulation.

    Final product types

    • Isoxazole-derived pre-emergent herbicide actives
    • Selective grass weed control products
    • Raw materials for regulatory data package submissions

    3. Advanced Chemical Research and Custom Synthesis

    Leading fine chemical synthesis service providers and life-science R&D centers specify this hydrochloride as a modular intermediate in tailoring bespoke heterocycle frameworks. Its use supports carbonyl derivatization, peptide mimetic synthesis, and probe molecule design—especially where customized isoxazole analogs furnish unique analytical or biological profiles. Operations must fulfill strict confidentiality, reproducibility, and analytical QA requirements to ensure reliable delivery for demanding research applications.

    Industry compliance standards

    • ISO 17025 Laboratory Accreditation for quality control
    • OECD Principles of Good Laboratory Practice (GLP)
    • Customer-specified analytical validation criteria
    • Material transfer safety regulations for research chemicals

    Typical usage ratio

    • Custom syntheses: 0.75–1.2 equivalents, tuned per stepwise substrate reactivity and desired scale (milligram to kilogram bench scale).

    Downstream process integration

    • Charged into solution-phase reaction vessels post-ring closure; in situ monitoring utilizes HPLC/LC-MS to optimize conversion with follow-up micro-scale purification by flash chromatography.

    Final product types

    • Custom heterocyclic research reagents
    • Bioactive probe molecules for screening
    • Peptidomimetic fragment libraries

    4. Specialty Fluorescent Tag and Label Synthesis

    Specialty chemical manufacturers produce fluorescent isoxazole tags for analytical and diagnostic use, exploiting this chloride’s selective reactivity for site-specific attachment to dye scaffolds. Quality-focused production incorporates cleanroom controls to prevent fluorescence quenching and cross-contamination, while each batch must maintain spectral purity for end-use in bioimaging or instrument calibration.

    Industry compliance standards

    • ISO 13485:2016 for medical device and diagnostic component supply
    • RoHS Directive 2011/65/EU for material purity and safety
    • General chemical GMP (where required for in vitro diagnostics)
    • Spectroscopic QC by internal SOP with required traceability

    Typical usage ratio

    • Selective tagging reactions: 0.8–1.05 equivalents, frequently dosed gradually under cooled conditions to control over-labeling and avoid background fluorescence.

    Downstream process integration

    • Introduced in final stage conjugation to fluorescent parent molecules; purification by preparative HPLC, with batch certification via fluorescence spectrometry before packaging for laboratory or diagnostic device integration.

    Final product types

    • Fluorescently labeled diagnostic agents
    • Bioanalytical dyes
    • Research-grade tagged peptides and small molecules
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    Certification & Compliance
    More Introduction

    Introducing 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carbonyl Chloride: Precision for Modern Synthesis

    Leaning on Years of Chemical Manufacturing Experience

    Walking the production floor every day, the importance of well-crafted intermediates stands out as the backbone for success in pharmaceutical and agrochemical innovation. In our pursuit of consistency and reliability, we bring forward 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carbonyl Chloride. Over the years, shifting requirements in custom synthesis have created a need for components that do more than pass a minimum threshold. End users look for products that build confidence batch after batch, without surprises or undetected variables. From sourcing raw materials with full transparency to refining every stage of synthesis, our facility stands rooted in discipline, patience, and continual improvement.

    Product Model and Specifications

    We produce 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carbonyl Chloride under tightly controlled conditions, using protocols developed by process chemists who stay informed on evolving customer demands. The product typically appears as a pale crystalline solid or sometimes as a finely divided powder, depending on customer specifications for downstream processes. Material is available in various lot sizes. Analysis verifies purity at levels suitable for sensitive downstream processes, focusing on the elimination of residual solvents, unreacted starting materials, and by-products. Each batch is reviewed for moisture content and trace metals according to standards set by users in complex molecule synthesis, especially those making the jump from lab scale to commercial production.

    The physical and chemical properties, including melting point, stability, and reactivity, align closely with what custom synthesis and API producers rely on. The product’s isoxazole core, methyl substitution, and specific arrangement of the 2-chlorophenyl group present synthetic opportunities that are not easily matched by other chlorinated isoxazole derivatives or by similar acyl chlorides lacking this constellation of substituents. Weight determination, proper packaging for moisture-sensitive shipments, and full batch traceability come standard, since we’ve learned firsthand the cost of shortcuts in this industry. The documentation provided with every order reflects years of input from end users who have made us tighten controls, improve traceability, and communicate more clearly.

    Application Insights from the Factory Floor

    Lab chemists and synthetic teams reach for 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carbonyl Chloride when constructing scaffolds for pharmaceuticals, crop-protection agents, and advanced materials. The compound’s unique combination of electronic and steric effects opens several reaction pathways that other standard acid chlorides or isoxazole intermediates simply cannot support. It acylates a wide array of nucleophilic partners, from amines to alcohols, often creating products with improved yield or cleaner reaction profiles. This has translated to fewer purification cycles downstream and higher throughput in process development projects.

    With strong deactivating effects from the 2-chlorophenyl group, users harness selective reactivity that streamlines the production of complex heterocycles and peptidomimetic products. Developers working on targeted therapies or enzyme inhibitors appreciate the functionality it brings, not just as a reactive partner but as a molecular fragment with a proven track record in lead identification and optimization projects. Unlike chlorinated acyl chlorides lacking the isoxazole ring, this compound offers building-block versatility while resisting unwanted side reactions, even in multi-step syntheses. Over years of close partnership with innovators, feedback has made it clear: the specific arrangement of atoms pays dividends during late-stage functionalization and combinatorial library diversification.

    What Sets This Compound Apart: Direct Experience Shows the Difference

    The specialty of 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carbonyl Chloride rests on its reliable performance in tough synthetic environments. Feedback from scale-up projects often focuses on how it tolerates less-than-ideal conditions during production. Unlike common carbonyl chlorides, this molecule resists degradation from light and oxygen better, and it remains stable in cold storage for extended periods. Our storage experience backs this up—material holds up without significant decomposition, and returns minimal impurity drift even after months on the shelf.

    We see major differences with similar isoxazoles that carry alternative substitutions. For example, switching the methyl group or the position of the chlorophenyl ring alters reactivity signatures, sometimes in subtle ways that only emerge during pilot production runs. Such experiences have made it clear that cosmetic similarities between isoxazole-4-carbonyl chlorides do not translate to identical performance. Our process development team tackles these differences early, testing across partner laboratories, so no user rounds a product development corner only to encounter a bottleneck.

    Custom reaction needs—such as controlled-release agrochemicals or tailored medicinal compounds—dictate selectivity and safety margins. Here, we’ve documented cases where researchers compared acyl chloride intermediates side-by-side and reported sharper selectivity from this molecule. This led to fewer downstream side products and enabled easier scale-up, directly influencing throughput and project timelines. Years of collaborating with R&D teams has shown that avoiding project delays depends on access to intermediates with documented, consistent behavior—not theoretical yield enhancements. Our crew handles each step with attention to both chemical performance and practical handling, since we know that success on paper means little unless it maps onto actual production.

    Operational Excellence Starts with Control, Ends with Trust

    Manufacturing fine chemicals involves more than mixing the right reagents. Our technicians and chemists manage each lot with the understanding that a single off-spec shipment has ripple effects across customer programs, timelines, and regulatory filings. We have learned through painful experiences that even minor impurity spikes can force partners into repeat work, wasted solvent, and regulatory headaches. So we invest in constant testing and equipment calibration not simply because protocols require it but because one misstep quickly becomes everyone’s problem.

    We recall several scenarios where third-party products underperformed, arriving with out-of-range assay values, high moisture, or unreported polymorphic forms. These incidents drive us to rely on in-house audits and high-frequency equipment checks. Batch records go deep into raw material sourcing and every intervention, building datasets over many campaigns. Any outlier gets flagged and immediately addressed, either by reprocessing or by complete batch rejection. This consistent vigilance yields not only better product but smoother relationships with our long-term partners, who’ve told us how critical this reliability becomes for late-stage development under tight deadlines.

    Fit for Scale-Up, From Kilos to Multi-Ton Lots

    No two clients handle intermediates the same way. Some need small custom lots for bench top trials; others demand reliable scheduling for multiple tons. We’ve grown processes alongside customers, mapping their feedback into our routines. Drying protocols, sieving, and packaging lines adapt to shipment requirements, whether the destination is a neighboring lab or a global API formulation site. We train logistics staff on the importance of prompt, careful delivery. Having addressed mishandling claims in the early years, we now place extra controls on loading, tracking, and secure transport. These lessons protect against delays and ensure product arrives in ready-to-use form.

    Our team recognizes that product waste or deviations quickly add up at large scales. Small improvements to yields or batch reproducibility translate into huge gains, especially when customers are bound to annual contracts. That’s why our process improvement team works hand in hand with R&D, taking feedback straight from customers’ shop floors and embedding it into our SOPs. Over time, this focus on unglamorous details—filter quality, transfer lines, residue collection—has paid off through repeat orders and expanded production commitments.

    Supporting Sustainable Progress in Chemical Synthesis

    Environmental responsibility is no longer optional. Many partners prioritize products that support greener chemistry, and we have responded by optimizing solvent systems, switching to renewable power sources where possible, and treating waste streams for minimal impact. Where the old approach favored speed over safety, the new standard rewards those who plan for both. Multiple rounds of process innovation allow us to run calorimetry studies, minimize hazardous by-products, and extend shelf-life without resorting to excess stabilizers. Reviews from independent auditors and client-led traceability checks all feed into continuous improvement, shaping not only how we make 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carbonyl Chloride but how we view our stewardship as a manufacturer.

    In our direct experience, making process changes that reduce reagent use or boost safety margin pays off twice: it builds loyalty with sustainability-minded customers and cuts long-term operational costs. We view every kilo produced as a chance to make a difference both for users in the lab and for the communities whose land, air, and water we share.

    Addressing Challenges Head-On: Our Real-World Solutions

    Complex intermediates like 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carbonyl Chloride introduce storage, handling, and recipe challenges. We listened as customers explained the cost of even minor moisture uptake, so we refined our storage protocols and now offer packaging tailored for low-humidity transit. Bulk orders come with options for nitrogen blanketing, and each package includes clear handling and storage guidance built from our lab and shipping experience.

    Solution stability ranks high in customer queries. We learned early that dissolution protocols impact downstream results, especially at the transition from DCM to greener solvents. We now guide partners on optimal solvent choices and share comparative stability data from multiple campaigns. Addressing real-world pain points means sharing knowledge beyond what one technician or chemist knows individually—instead, we bundle generations of process insights into every order.

    Transporting sensitive intermediates across borders used to take days of paperwork and uncertainty. Now, thanks to pre-approved documentation packages and careful coordination with freight specialists, we keep regulatory surprises to a minimum. We acknowledge that delays cost more than money—they risk whole project lifecycles. We urge every partner to check local regulations proactively and share any anticipated hurdles early. It’s a partnership built on the knowledge that good manufacturing never ends at the factory gate.

    Safety and Transparency as Core Values

    Our story as a manufacturer includes learning from incidents where a lack of transparency led to cascading problems. Today, every batch of 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carbonyl Chloride ships with full trace documentation, COAs, detailed impurity profiles, and clear guidance material. Customers have shown that access to up-to-date information speeds up validation and material opening, and builds confidence, especially where audit schedules tighten.

    We also promote open dialogue. Our staff picks up the phone, answers tough questions, and tracks unresolved issues with the urgency they deserve. Whether it’s a question about an obscure impurity or a delivery hiccup, our team handles it with the seriousness it warrants. We see tangible results: incorrect assumptions get corrected swiftly, solutions get implemented by operators who understand the risks involved, and project partners move up their schedules, not down. Our cumulative experience has taught us that transparency and urgency save both time and reputation.

    Conclusion: Backed by Experience, Constantly Evolving

    Since stepping into chemical production, the lessons surrounding product reliability and user trust have shaped us. Producing 3-(2-Chlorophenyl)-5-Methylisoxazole-4-Carbonyl Chloride is not just a technical achievement but a matter of daily choices involving ethics, worker training, and attention to customer needs. This is a product built on countless small improvements, tested and refined in real plants, and judged not by claims but by the satisfaction and ongoing business of long-standing partners.

    Every kilogram manufactured is a result of hands-on effort, lessons learned, and a commitment to keep evolving. The teams here continue to listen to the field, implement operational upgrades, and deliver a product that advances innovation for those at the front lines of molecular discovery. The difference between success and headache, in our direct experience, often comes down to having a partner who knows the territory, takes responsibility, and delivers as promised. That has always been the foundation for lasting work in this industry.