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4-Chloro-6,7-Dimethoxyquinazoline

    • Product Name 4-Chloro-6,7-Dimethoxyquinazoline
    • Alias 4-Chloro-6,7-dimethoxyquinazolin
    • Einecs 629-96-1
    • 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
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    Specifications

    HS Code

    339763

    Product Name 4-Chloro-6,7-Dimethoxyquinazoline
    Chemical Formula C10H9ClN2O2
    Molecular Weight 224.65 g/mol
    Cas Number 21187-22-4
    Appearance White to off-white crystalline solid
    Melting Point 172-175°C
    Purity Typically ≥98%
    Solubility Soluble in DMSO, slightly soluble in water
    Storage Conditions Store at 2-8°C, keep tightly closed
    Smiles COC1=C(C2=NC=NC(Cl)=C2C=C1)OC
    Inchikey PVFJZLKOPAKZSR-UHFFFAOYSA-N

    As an accredited 4-Chloro-6,7-Dimethoxyquinazoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 10g quantity of 4-Chloro-6,7-Dimethoxyquinazoline is supplied in a sealed amber glass bottle with tamper-evident cap.
    Shipping 4-Chloro-6,7-Dimethoxyquinazoline is typically shipped in sealed, clearly labeled containers to prevent contamination or leakage. The chemical is handled as a non-hazardous material under standard shipping regulations. It is protected from moisture and direct sunlight, with documentation provided for proper identification and compliance with international transport standards.
    Storage Store **4-Chloro-6,7-Dimethoxyquinazoline** in a tightly sealed container, away from light and moisture, at room temperature (15–25°C). Keep in a well-ventilated, dry area designated for chemicals, away from incompatible substances such as strong oxidizers. Properly label the container and ensure restricted access to authorized personnel. Use appropriate precautions to prevent inhalation, skin, or eye contact.
    Application of 4-Chloro-6,7-Dimethoxyquinazoline

    Applications of 4-Chloro-6,7-Dimethoxyquinazoline in Industrial Manufacturing

    As a trusted upstream manufacturer, we deliver 4-Chloro-6,7-Dimethoxyquinazoline for specialized industrial sectors requiring high-purity heterocyclic building blocks. Below are the principle downstream segments relying on our material for advanced synthesis and end-product quality.

    1. Pharmaceutical Intermediates: Tyrosine Kinase Inhibitor Synthesis

    Leading pharmaceutical producers select our compound as a core intermediate for the synthesis of quinazoline-based tyrosine kinase inhibitors, central to anticancer agent development. Its chloro and methoxy groups facilitate key N-arylation and substitution reactions in multistep synthesis. The intermediate integrates after halogenation and before coupling processes. Compliance with ICH Q7 and regional pharmacopoeias remains mandatory, and purity above 99% minimizes impurity transfer downstream. Analytical controls ensure consistent performance in pilot and commercial-scale production, with continuous feedback integrated from peptide coupling and hydrogenation steps through to the final active pharmaceutical ingredient (API) formation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (EP) monographs for raw materials
    • US FDA 21 CFR Part 211 for pharmaceutical manufacturing controls
    • Chinese Pharmacopoeia raw material requirements

    Typical usage ratio

    • 0.5–1.5 molar equivalents compared to the substrate, adjusted according to the synthetic pathway and efficiency in arylation/cyclization reactions

    Downstream process integration

    • Added post-halogenation in stepwise API synthesis route, prior to coupling with aniline or other amines during the heterocycle assembly
    • Charged under nitrogen at 0–25°C to minimize decomposition
    • Integrated into multi-stage batch or continuous flow reactors for kinetic profile optimization
    • Subject to in-process HPLC and residual solvent testing prior to API isolation

    Final product types

    • Gefitinib, Erlotinib, and other quinazoline-based anticancer APIs
    • Small molecule drug substances featuring quinazoline core

    2. Agrochemical Active Ingredient Precursors

    Key agrochemical manufacturers source this specific heterocycle for use in the synthesis of selective herbicide and fungicide active ingredients. The compound enters as a precursor in multi-step synthetic sequences that enable regioselective functionalization, leading to finished actives with high crop safety profiles. Downstream processes require robust material traceability and validation, while adherence to FAO and OECD guidelines is essential. The raw material’s chemical stability supports repeated batch cycles, and feedback from downstream sulfonation or amidation steps help optimize dosing and yield.

    Industry compliance standards

    • FAO Specification for Plant Protection Products
    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 9001:2015 Quality Management Systems
    • Local Ministry of Agriculture chemical registration protocols

    Typical usage ratio

    • 0.8–1.3 molar equivalents in precursor-to-active synthesis steps—tuning based on conversion rate in initial nucleophilic substitution sequence

    Downstream process integration

    • Material dissolved in DMF or DMSO before entering alkylation reactors
    • Reacted under controlled temperature and time after seeding to primary coupling reaction
    • Monitored for specific impurities (CQC, total residual solvents)
    • Transferred under inert gas to downstream formulating tanks for actives crystallization

    Final product types

    • Quinazoline-based herbicide technical concentrates
    • Novel systemic fungicide intermediates

    3. Chemical Research: Heterocyclic Scaffold for Advanced Synthesis

    Chemical and pharmaceutical R&D groups in both industrial and academic settings use our raw material as a reliable scaffold for advanced heterocyclic synthesis and SAR (structure-activity relationship) screening. It enables rapid analog generation through selective substitutions in the aromatic system. Laboratories benefit from our analytical COA support and secure batch-to-batch consistency, and downstream chemistry teams scale reactions directly from gram to multi-kilogram lots for pilot studies. Proper documentation supports repeatable process design and transfer. R&D use obeys global safety and handling protocols to manage exposure risks for research staff.

    Industry compliance standards

    • OECD Guidelines for Chemical Testing
    • ISO 17025 Laboratory Accreditation (analytical quality control)
    • Internal chemical safety and waste management SOPs (aligned with REACH Annex XVII)
    • Material Safety Data Sheet (MSDS) and GHS labeling conventions

    Typical usage ratio

    • 0.2–1.0 molar equivalents in parallel reaction optimization, varying according to the scaffold diversification route

    Downstream process integration

    • Charged into small-scale batch reactors for initial analog synthesis
    • Used as a starting block in Suzuki, Buchwald coupling, or nucleophilic aromatic substitution reactions
    • Implemented in microfluidic synthesis or solid-phase protocols for high-throughput screening
    • Recovered and purified by column chromatography or preparative HPLC for further modification

    Final product types

    • Novel heterocyclic library compounds for drug discovery
    • Reference standards for analytical method development
    • Academic publications and patent disclosures

    4. Electronic Chemicals: Precursors for High-Performance Polymer Synthesis

    The electronics manufacturing sector incorporates our raw material into the synthesis of specialty polyquinazolines, sought for their dielectric and thermal resistance in advanced circuit components. Precise control over substitution on the quinazoline core enables tuning of polymer chain alignment and resistivity. Factories perform strict pre-shipment analysis to guarantee trace metallic and halide content below process interference thresholds. Real-time feedback from polymerization steps and post-production dielectric assessment informs the input ratio and blending sequence. Compliance with RoHS and local electronic chemical management codes governs raw material selection and documentation.

    Industry compliance standards

    • Restriction of Hazardous Substances (RoHS) Directive, 2011/65/EU
    • IEC 62474 Material Declaration
    • ISO 14001 Environmental Management Systems for electronics manufacturing
    • JIS C 0950 (Japan) hazardous substance management

    Typical usage ratio

    • 10–30% by weight in consumer or industrial polyquinazoline resin batches, modulated for dielectric, solubility and film-forming balance

    Downstream process integration

    • Introduced during initial monomer charge for condensation polymerization
    • Dissolved or suspended in high-purity solvents under cleanroom conditions
    • Catalyzed or co-polymerized with diamines or diacids
    • Polymers processed into films, coatings or composites in dedicated laminar flow assembly lines

    Final product types

    • Dielectric polyquinazoline films
    • Advanced circuit board coatings
    • Heat-resistant plastic housings for semiconductor applications
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    Competitive 4-Chloro-6,7-Dimethoxyquinazoline prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    4-Chloro-6,7-Dimethoxyquinazoline: Quality and Value from the Manufacturer's Perspective

    Understanding 4-Chloro-6,7-Dimethoxyquinazoline: Background and Application

    As a manufacturer with deep roots in the synthesis of quinazoline derivatives, I’ve seen the critical role compounds like 4-Chloro-6,7-Dimethoxyquinazoline play in the growth of both pharmaceutical research and chemical development. The molecule’s profile — with its chlorine atom at the 4-position and methoxy groups at the 6 and 7 positions on the quinazoline skeleton — offers a unique combination of reactivity and stability. Over the years, we have refined our systems and processing techniques to ensure this product leaves our plant with the precise quality chemistry demands.

    Our daily routine involves closely monitoring every batch from raw material assessment through reaction, purification, and final quality checks. Precision at every step matters, and the importance of methodical operation can’t be overstated when a slight deviation in temperature, pH, or solvent composition might impact the final outcome — even though the target structure seems simple at first glance. There’s a lot more to making a pure, reliable 4-Chloro-6,7-Dimethoxyquinazoline product than just combining reagents according to published methods. Small procedural optimizations, process tweaks, and—to be honest—a fair share of practical setback sharing among our chemists have guided our approach.

    A Glimpse at Our Specifications and Model Approach

    In-house, we catalogue our 4-Chloro-6,7-Dimethoxyquinazoline under a practical identification system that aligns batch numbers, production dates, and spectroscopic signatures — these details matter far more than catchy labels. The real substance of our product rests in its specifications: purity by HPLC above 98%, tightly consistent melting point range, fine powder morphology, and trace residue controls to meet even the lowest class impurity thresholds. We treat every specification as more than a checkbox. You’ll see us pulling extra samples, double-checking GC-MS data, and running repeated TLCs to pick up any hint of residual starting materials or unintended by-products.

    During manufacturing, every critical stage goes through analysis to ensure robust quality. We store material in controlled environments to avoid any shifts in moisture or contamination. Final packaging reflects a pragmatic recognition of lab realities: sealed containers for protection, clear labelling for traceability, and batch records with analytical data attached, not just stored on a server somewhere out of sight.

    What Sets 4-Chloro-6,7-Dimethoxyquinazoline Apart: A Manufacturer’s Insight

    The number of quinazoline derivatives on the market might feel overwhelming to a new researcher, but 4-Chloro-6,7-Dimethoxyquinazoline stands out thanks to its versatility in downstream chemical transformations. We've seen customers leverage it as a scaffold in kinase inhibitor research, where the methoxy groups improve solubility while the reactive chlorine facilitates nucleophilic substitutions. This makes it an ideal entry point for synthesizing a wide range of heterocyclic compounds, and our team has worked closely over time with pharmaceutical developers pursuing SAR (structure–activity relationship) studies in oncology, anti-inflammatory, and CNS drug programs.

    What creates a tangible difference isn’t just the base structure – subtle differences in trace impurities, crystal form, and batch-to-batch consistency can make or break an advanced synthesis. Unlike similar quinazoline derivatives that feature electron-withdrawing groups in less accessible positions, our product offers reliable activation potential at the 4-position, allowing a broader range of couplings and substitutions under mild conditions.

    Manufacturing this molecule in-house gives us close oversight at every stage. That oversight translates into tighter quality controls and rapid response to customer feedback. This isn’t a product we source from bulk catalogs and repackage; our process includes continuous monitoring, targeted purification steps, and a direct connection between chemical engineering and application. Lab chemists often need to tweak their conditions on the fly, which is only possible if their starting materials perform consistently each time. Skimping on in-process analytics or cutting corners in drying and packaging just leads to headaches downstream — a situation I’ve watched play out too many times at facilities trying to stretch their margins.

    Usage in Research and Advanced Synthesis

    Research groups working on targeted therapies, crop science, or even materials chemistry value a compound that lets them run late-stage functionalizations with confidence. In our experience, projects succeed or struggle depending on the reliability of each small molecule component. There’s a real-world impact to a failed coupling, interrupted scale-up, or unexpected side-product formation. Our job as a manufacturer is to minimize those variables.

    From the bench to pilot scale, labs look for predictability — tight melting point specification, full lot-to-lot NMR comparability, and freedom from extraneous contaminant peaks. As we continue to produce and supply 4-Chloro-6,7-Dimethoxyquinazoline, we engage directly with users to hear firsthand how the material functions in actual synthetic campaigns. The collective knowledge from those interactions has helped us adjust drying protocols, modify solvent handling procedures, and identify packaging solutions that extend shelf-life and simplify inventory management in real-life lab settings. We never underestimate how real lab conditions—open air transfers, room temperature storage, high humidity spells—can affect a compound’s reactivity and longevity.

    Subtle handling differences between batches can change the fate of an advanced synthesis. For example, small traces of by-products not detected in basic TLC might poison a palladium-catalyzed reaction or cause color issues in preparative chromatography. To counteract these risks, we regularly review and revise our standard operating protocols and invest in advanced detection technologies: not just to meet a published technical requirement, but to accommodate the real hurdles our partners describe in their work.

    How Our Hands-On Approach Supports Innovation

    Beyond analytical chemistry, there’s a human element at play in manufacturing 4-Chloro-6,7-Dimethoxyquinazoline. Our production chemists keep logs of process anomalies, jot down practical notes, and share experience during shift transitions. This forms a living record that cycles back into process development — small discoveries that never make the published literature but often mean the difference between “it worked” and “why did it fail this time?” We actively encourage questions from customers and share up-to-date certificates with supporting raw spectral data rather than just relying on the technical sheet send-out.

    We’ve learned that real value creation arises from close communication between manufacturer and end-user. Early on, requests for smaller-scale, pilot-sized lots prompted us to invest in flexible reactor setups. A few years back, one research group reached out after encountering solubility issues in DMSO. Our investigation traced the problem to subtle humidity absorption during a humid summer run, prompting us to overhaul our desiccation protocol and introduce a new packaging format. The feedback loop between pilot plant floor and application chemists in the field remains a cornerstone of our operation.

    Comparisons with Nearby Derivatives: What Really Matters

    On the market, you’ll find other quinazolines with swapping substituents—unsubstituted 4-chloroquinazolines, methoxy analogs lacking the chloro group, and positionally shifted methoxy derivatives. Differences might seem minor on paper but, at scale, they shift how these compounds behave in synthetic routes.

    Our product’s particular arrangement—chlorine at 4, methoxy at 6 and 7—means electron distribution across the ring opens up the molecule to efficient functionalization. Direct nucleophilic displacement at the 4-position outperforms analogs with more hindered substituents, and the double methoxy substitution at 6 and 7 increases solubility over unsubstituted parents, streamlining work-ups and filtrations. Chemists trying to access certain heterocyclic frameworks find our compound reacts cleanly in Suzuki couplings, SNAr substitutions, and is amenable to regioselective modifications that can become either a headache or a breeze depending on how cleanly the starting material performs.

    Other derivatives sometimes show a propensity for partial hydrolysis, decomposition in open air, or fail to provide sharp melting points, which complicates purity assessment. We’ve worked through the pain of batch rejection more times than we care to admit—each time using those lessons to tighten up everything from source material quality checks to in-process solvent profiles.

    Meeting Industry Challenges: Quality, Safety, and Responsibility

    As both supplier and manufacturer, our obligation extends beyond just technical compliance or price. We keep up with evolving best practices for chemical stewardship — handling waste management, exposure control, and personnel safety as part of day-to-day operations. From procurement to pre-shipment, our audit teams assess new sources of raw materials by not just reviewing certificates but inspecting supplier facilities and shipping lanes. This hands-on scrutiny has allowed us to weed out upstream inconsistencies that might otherwise slip by.

    We’ve approached every regulatory challenge head-on, not by aiming for minimum requirements but by driving toward practical reliability in application. For packaging, we avoid repurposed containers that might introduce residual contaminants or compromise physical integrity. With storage, we confirm thermal and chemical stability through real-time shelf-life studies carried out on-site, instead of speculative projections.

    When problems arise—be it labeling misprints, transit delays, or supply interruptions—we chase down root causes and communicate transparently with our partners. Our operations team keeps customer relationships active, arranging support calls for troubleshooting, and sharing application notes direct from our development chemists. In one case, a misaligned shipment was traced to a last-minute customs change affecting air-dry protocols. Rather than glossing over it, we rewrote shipping scripts and tested new tamper-evident seals to guarantee traceability and purity through every handoff.

    Supporting Research and Development with Real-World Solutions

    Success in research chemistry depends on more than catalog descriptions and published spectra. Our R&D team is committed to solving application-based questions, often modifying production schedules or running extra small-lot preparations on short notice for partners racing an internal deadline. We get direct feedback on solubility, reactivity, and compatibility from those synthesizing libraries or scaling up for animal studies, and we build that learning back into our process.

    Several years of producing 4-Chloro-6,7-Dimethoxyquinazoline have shown us that new applications crop up almost constantly—in kinase inhibitor development, as an intermediate in dye chemistry, or as a step in agricultural product synthesis. Each application brings new parameters: unexpected side-products, temperature or pH sensitivities, and downstream requirements for reactivity or purity. We don’t just provide a static product; we keep communication lines open and adapt process parameters or quality assessment points as needed.

    It’s common for researchers to request batch-specific details, spectral overlays, or even custom pilot-scale syntheses. We’re used to handling those needs quickly—sampling, analyzing, and sharing up-to-date documentation. In our shop, that means reallocating dedicated reactors, assigning chemists to review protocols, and cycling raw material supplies.

    Trust Built from Experience and a Commitment to Quality

    Quality in 4-Chloro-6,7-Dimethoxyquinazoline isn't a matter of marketing claims — it's the result of repeated investments in training, infrastructure, and hands-on experience. Chemists on our floor undergo ongoing education on analytical instrumentation, solvent handling, and emergency protocols. We schedule periodic reviews of analysis sheets, review any flagged QC events as a group, and continually strive to cut down cycle times without cutting quality.

    The value of a consistent, reliable supply stream shows up whenever researchers are scaling up or pushing a new method toward publication or industrial application. A single contaminant can invalidate a full library screen or clinical precursor batch, causing real delays and costs. Having upstream control—batches produced, analyzed, and tracked by the same team—enables us to guarantee tighter tracking than any third-party broker or distant repacker can offer.

    Every time a customer shares feedback, positive or negative, the notes get logged in our application file. That evidence often turns into the next baseline for in-process checkpoints or packaging modifications. Whether it’s additional desiccation for tropical labs, smaller aliquots for fast-turn programs, or specialized documentation for regulatory bodies, our processes always cycle back to real-world performance.

    Sustaining Value Through Trust and Transparency

    The work of a chemical manufacturer rarely makes headlines, but the indirect value delivered through reliable small molecule production shapes the future of pharmaceutical, agricultural, and materials science. Our practical, hands-on experience manufacturing 4-Chloro-6,7-Dimethoxyquinazoline informs every batch and every interaction. We support not only the technical requirements of advanced synthesis but also the shifting, pragmatic needs of working research chemists.

    Producing and supplying a product countless downstream reactions depend on carries a genuine sense of responsibility. We measure our success by how reliably our product enables the next step in innovative research. As we move forward, our team keeps listening, learning, and adjusting — making sure that when our partners ask for 4-Chloro-6,7-Dimethoxyquinazoline, they receive not just a reagent but the collective expertise of dedicated chemists, engineers, and quality specialists backing their next breakthrough.