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5-Bromo-2,4-Dimethoxypyrimidine

    • Product Name 5-Bromo-2,4-Dimethoxypyrimidine
    • Alias 5-Bromo-2,4-dimethoxy-pyrimidine
    • Einecs EINECS 610-041-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    368179

    Chemical Name 5-Bromo-2,4-Dimethoxypyrimidine
    Cas Number 88584-40-5
    Molecular Formula C6H7BrN2O2
    Molecular Weight 219.04
    Appearance White to off-white solid
    Melting Point 64-68°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents (e.g., DMSO, methanol)
    Smiles COC1=NC(=C(Br)N=C1)OC
    Inchi InChI=1S/C6H7BrN2O2/c1-10-5-3-8-6(11-2)4(7)9-5/h3H,1-2H3
    Storage Conditions Store at room temperature, protected from light and moisture
    Synonyms 5-Bromo-2,4-dimethoxypyrimidine

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

    Packing & Storage
    Packing 5-Bromo-2,4-Dimethoxypyrimidine is supplied in a sealed 25g amber glass bottle, labeled with safety, chemical name, and CAS.
    Shipping 5-Bromo-2,4-Dimethoxypyrimidine is shipped in tightly sealed containers under ambient conditions. It is packaged according to international regulations for chemical safety, ensuring protection from moisture and light. Appropriate hazard labels are used, and all documentation accompanies the shipment to ensure compliant handling and transport. Special care is taken to avoid breakage and spills.
    Storage 5-Bromo-2,4-Dimethoxypyrimidine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and heat sources. Keep it away from incompatible substances such as strong oxidizers. Store under inert atmosphere if possible, and clearly label the container. Ensure proper chemical hygiene and restrict access to trained personnel only.
    Application of 5-Bromo-2,4-Dimethoxypyrimidine

    Applications of 5-Bromo-2,4-Dimethoxypyrimidine in Industrial Manufacturing

    5-Bromo-2,4-Dimethoxypyrimidine serves as a critical intermediate in several industrial sectors, especially those requiring high-purity heterocyclic compounds for demanding end uses. Below are the principal application scenarios based on actual downstream demand, each with specific compliance, formulation, process, and finished product considerations.

    1. Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical manufacturers use 5-bromo-2,4-dimethoxypyrimidine in the synthesis of advanced pharmaceutical intermediates, such as kinase inhibitors and antiviral compounds. During multi-step synthesis, this raw material is often brominated and combined with complementary nucleophiles to construct critical pyrimidine-based scaffolds. This approach supports proprietary process routes where raw material purity and trace element limits affect final drug batch quality. Enterprises typically deploy this intermediate in GMP-compliant, closed-system batch reactors with rigorous analytical controls on residual solvents and heavy metal impurities, ensuring that each batch can progress to downstream active substance formation under validated protocols.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice
    • USP General Chapter <823> Radiopharmaceuticals
    • Ph. Eur. purity requirements for APIs
    • 21 CFR Part 211 (US FDA cGMP for finished pharmaceuticals)

    Typical usage ratio

    • Intermediate charge: 0.18–0.35 molar equivalents per API batch, precise adjustment based on target structure and downstream conversion yield.

    Downstream process integration

    • Enters as pyrimidine-building intermediate during amidation, coupling, or cyclization steps of heterocycle API synthesis
    • Added post-primary solvent charge and pre-reactant addition
    • Quality testing performed at incoming RM stage and in-process blending

    Final product types

    • Anti-cancer kinase inhibitors (e.g. BRAF or EGFR inhibitors)
    • Antiviral compounds (nucleoside analog pharmaceuticals)
    • Pyrimidine-based CNS active ingredients
    • API intermediates for further downstream modification

    2. Agrochemical Synthesis (Herbicides and Fungicides)

    The agrochemical sector applies 5-bromo-2,4-dimethoxypyrimidine in the formulation of active molecules used in crop protection chemistry. This compound functions in a key step of the synthetic sequence for modern heterocyclic herbicides and some systemic fungicides. The material’s bromine position and dimethoxy substitution facilitate targeted functionalization, helping achieve high selectivity and low off-target bioactivity in the finished actives. Typical processes run in closed reactors to prevent cross-contamination, and downstream buyers audit supplier QC data as part of mandatory global agrochemical stewardship protocols.

    Industry compliance standards

    • FAO/WHO Specification Requirements (JMPS/CPP)
    • OECD Good Laboratory Practice (GLP)
    • SANCO/12592/2012 (EU active substance technical equivalence)
    • ISO 9001:2015 (Quality Management Systems for bulk intermediates)

    Typical usage ratio

    • Intermediate feed: typically 22–28% by weight of precursor charge per active ingredient synthesis; ratio adjusted depending on targeted molecule and batch scale.

    Downstream process integration

    • Charged at the halogen exchange or Suzuki coupling step
    • Mixed with specific metal catalysts and anhydrous bases to derive unique heterocyclic backbones
    • QC sample taken at every critical process control point

    Final product types

    • Heterocyclic herbicides (e.g. triazine, pyrimidine-based)
    • Systemic cereal and fruit fungicides
    • Pre-emergent and post-emergent weed control agents
    • Technical-grade agrochemical active compounds

    3. Fine Chemical Building Block for Organic Synthesis

    Contract manufacturers and specialty chemical producers use 5-bromo-2,4-dimethoxypyrimidine as a key building block for downstream preparation of complex heterocyclic compounds, which are further employed in electronic materials, dye intermediates, and advanced organic synthesis. Its double methoxy groups and bromine atom enable numerous cross-coupling or substitution reactions under controlled catalytic conditions. These fine chemicals often require compliance with customer-specified analytical thresholds for trace organics and metal residuals, with regular in-line quality verification in continuous production environments.

    Industry compliance standards

    • REACH (EC 1907/2006) for chemical safety
    • ISO 9001:2015 (QC systems for intermediates)
    • Customer-specific impurity profile requirements
    • Internal Environmental Management Systems (ISO 14001 where required)

    Typical usage ratio

    • Compound loading: 5–15% by total raw material mass depending on specific downstream reaction and final target molecular complexity.

    Downstream process integration

    • Introduced as primary heterocyclic substrate at catalytic coupling, Suzuki, or Buchwald-Hartwig step
    • Metered addition into automated reactors, monitored by in-line HPLC or GC
    • QC holds at every compounding step for trace bromide and residual solvent analysis

    Final product types

    • Specialty pyrimidine derivatives for organic electronics
    • Photoactive and pigment intermediates
    • Pyrimidine-based fine chemicals for downstream dye synthesis
    • Intermediates for next-generation materials and high-purity reference substances

    4. Discovery Chemistry for Custom R&D Libraries

    CROs (Contract Research Organizations) and pharmaceutical R&D labs demand 5-bromo-2,4-dimethoxypyrimidine for early-stage medicinal chemistry and rapid library synthesis. The compound’s brominated aromatic system and dual methoxy substitution allow chemists to conduct rapid parallel screening, facilitating efficient SAR (structure-activity relationship) development for novel compound discovery. Laboratory-scale processes include small-batch, liquid-phase synthesis, with strict traceability and batch documentation for every library pool, in accordance with global regulatory expectations for preclinical candidate development.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • USP general guidelines for reference standards
    • Internal R&D process traceability as per customer project requirements
    • ISO 9001:2015 for R&D project traceability and documentation

    Typical usage ratio

    • Library synthesis input: 1.0–1.2 equivalents per target molecule in split-pool or parallel array format, tailored for each combinatorial block.

    Downstream process integration

    • Serves as electrophilic partner for Suzuki, Stille, or Buchwald-Hartwig couplings
    • Enters one-pot procedures for rapid analogue creation
    • Documented in ELN (Electronic Lab Notebook) with full batch provenance

    Final product types

    • Fragment libraries for early drug discovery
    • SAR compound arrays for high-throughput screening
    • Lead optimization intermediates
    • Custom reference standards for industry and academic partners

    5. Advanced Material Intermediates for Specialty Polymers

    Producers of advanced specialty polymers incorporate 5-bromo-2,4-dimethoxypyrimidine as a functionalized monomer precursor in select polymerization processes, notably those targeting high-performance materials with tailored electrical or barrier properties. The compound’s nucleophilic methoxy groups and bromine enable custom cross-linking and ring-opening reactions, realized through controlled catalyst and thermal input conditions. Downstream integration requires batch traceability and certification of low halogen residuals, consistent with polymer electronic or optical grade standards.

    Industry compliance standards

    • ISO 9001:2015 for polymer intermediates
    • ASTM D6288-10 (QC procedures for specialty polymer raw materials)
    • RoHS Directive 2011/65/EU for electronic applications
    • Customer-specific residual halogen and extractables testing

    Typical usage ratio

    • Functional monomer charge: 8–14% by polymer blend weight; tailored based on target mechanical and electrical properties in the end material.

    Downstream process integration

    • Introduced during catalyst-initiated co-polymerization or prepolymer mixing stage
    • Monitored using in-line spectrometry for compositional accuracy
    • Integrated as functional co-monomer for cross-linked and specialty hybrid polymer matrices

    Final product types

    • High-performance electronic encapsulant polymers
    • Engineered optical barrier films
    • Custom cross-linked coatings for advanced electronics
    • Specialized polymeric materials for electrical or optical use
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    Certification & Compliance
    More Introduction

    5-Bromo-2,4-Dimethoxypyrimidine: Our Experience with This Key Intermediate

    What Sets 5-Bromo-2,4-Dimethoxypyrimidine Apart in the Chemical Landscape

    Walking through the syntheses that shape modern pharmaceutical and agrochemical development, certain intermediates tend to show up again and again. Among these, 5-Bromo-2,4-Dimethoxypyrimidine stands out by bridging reliability with direct functionalization potential. We manufacture this pyrimidine derivative not as a sideline, but as part of an integrated catalog of halogenated heterocycles, supporting R&D groups and production chemists who depend on consistent, precise building blocks.

    We’ve spent years refining the process for preparing 5-Bromo-2,4-Dimethoxypyrimidine. Our batches maintain tight color and purity controls, and our teams monitor not only the major specifications but also subtle by-product contamination points. In comparative experience with similar pyrimidines—like non-brominated or non-methoxylated analogs—the bromine on the 5-position and the methoxy groups make a real difference in reactivity and solubility. The compound dissolves well across several organic solvents, so customers typically report easier adaptation into both bench and pilot-scale reactors.

    Why So Many Chemists Return to This Intermediate

    The methoxy substituents at 2 and 4 positions boost not only the electron density of the ring but also moderate the reactivity of coupling partners. In Suzuki and Buchwald–Hartwig reactions, the bromine at the 5-position provides a reliable handle. It doesn't demand exotic conditions to substitute efficiently. For anyone who has worked through the frustrations of under-reactive, over-deactivated, or poorly soluble intermediates, that straightforward handling reduces headaches and cuts down on failed runs.

    We have supported medicinal chemists looking to introduce diverse side chains onto the ring structure, as well as process teams developing multistep synthesis of drug candidates or intermediates for crop protection. The shelf-life and batch consistency of our material get mentioned in feedback from several customers, especially when compared to older stocks held too long by third-party distributors.

    Practical Insights on Handling and Storage—What’s Worth Knowing

    For anyone on the other end of the chain, receiving drums and kilos instead of vials, practical issues come quickly into focus. Over several years of direct manufacturing, we have learned which drum linings matter for this product and what atmosphere to use during transportation. Sample retention and tracking have flagged rare degradation events, usually linked more to storage conditions than to inherent instability. Under standard ambient conditions, the crystalline powder holds up well, and it does not release fumes or odors, making it easier for downstream users to avoid nuisances in open-vessel workups.

    Shipping, even overseas, brings its own considerations. Moisture control matters less for 5-Bromo-2,4-Dimethoxypyrimidine than for some highly hygroscopic heterocycles. Still, we use double-lined PE bags and containers with verified seals, based on the odd incident of trace-water ingress during very long customs delays. Customers doing automated dispensing or solid-phase chemistry particularly appreciate the consistent particle size, because it flows predictably and resists caking.

    Comparative Reaction Experience with Related Pyrimidines

    Labs that use both the bromo and chloro analogs often share feedback about selectivity. Bromine, by nature, leaves at lower temperatures than chlorine during cross-coupling, with fewer side reactions. Some groups try to swap methyl or ethyl for the methoxy groups but end up with more stubborn by-products in later steps, likely owing to the oxygen content making deprotection smoother or acting as a tunable site for further transformation. Years in production scale-up have shown that the switch to the bromo, dimethoxy compound eliminates at least one or two purification headaches for many users.

    Screening through analogs may yield other interesting substitution patterns, but this compound stays at the top for those pursuing arylamine, aryl, or heteroaryl derivatives via Pd catalysis. The formation of C-C or C-N bonds becomes less of a tactical gamble and more of a reliable workflow.

    Specifications We’ve Learned Matter Most

    Most inquiries begin with CAS number or a general request for “high purity.” Over time, we’ve learned to ask what reaction or transformation the chemist is running. Trace impurities that go unnoticed in one coupling step can follow through and complicate late-stage purification. Our internal benchmark for assay is routinely over 99%, with targeted controls on moisture, heavy metals, and residual solvent. We minimize the alkali and acid residuals that can damage sensitive catalysts.

    Anecdotally, returning customers often mention lot-to-lot reproducibility. In-house, we have improved our crystallization and drying cycles to prevent the carryover of high-boiling byproducts—a problem that plagues poorly controlled runs. QC checks include not just HPLC and GC, but also in-depth NMR and Karl Fischer titrations. Our experience with customer returns, almost always from improper storage by handlers, teaches us to support clients in finding robust in-lab protocols.

    Feedback from the Field—User Experience Beyond the Factory

    One of our longstanding partners, a specialty API producer, scaled up a lead structure requiring several hundred kilos per batch, running a metal-catalyzed amination on our 5-Bromo-2,4-Dimethoxypyrimidine. He described a “night and day” difference in reaction yield and workup purity after switching from multi-sourced intermediates to our direct material. Another process chemist commented that competitor samples “sometimes darkened on the shelf within weeks,” while our crystalline product remained colourfast through long-term storage.

    Research chemists using this intermediate in fragment-based drug design emphasize the reliability for high-throughput screening. “No lottery,” as one said, “just the product as described, every time.” When customers report trouble, our support team can access the retained sample, confirm fingerprint spectra, and walk through their workup. Regular communications with end-users help us catch rare but critical points where an unexpected impurity—not detected in routine QC—can show up in very low-yield coupling runs.

    Quality, Traceability, and Regulatory Aspects

    As a manufacturer engaged with both domestic and export markets, we must comply with a patchwork of regulations. Years of document preparation and regulatory submission have added depth to our traceability protocols. Customers in Europe and North America, in particular, value access to up-to-date safety data and documentation. This means full batch traceability, which supply chain disruptions have demonstrated is not an optional extra.

    By keeping documentation seamless and providing real-time support rather than generic certificates, we maintain repeat partnerships. Unexpected situations, like customs inspections or recalls, call for quick access to original analytical data and batch certificates. We do not outsource these steps; our own manufacturing records cover every lot from precursor to QC release, with all line items auditable. Having been through a few audits ourselves, we know the difference that on-the-ground data can make.

    Commitment to Sustainability and Environmental Responsibility

    Sustainability in chemical manufacture is not just a slogan, especially as clients in pharmaceuticals and crop protection face pressure for greener, safer processes. Producing 5-Bromo-2,4-Dimethoxypyrimidine challenges us to balance efficient halogenation and methylation with minimal waste generation. Over the last few years, we have improved our process to reclaim solvents and minimize effluent bromides—key steps in balancing quality production with environmental stewardship.

    We invested in stricter in-line monitoring of waste streams, catching process drifts before they scale. Safe bromine handling and closed-loop methylation further reduce emissions and operator risk. Some clients ask specifically about environmental impact reports. We provide clear, data-based assessments rather than marketing gloss, listing real reductions in energy and waste output as our methods mature.

    Trends in the Use of 5-Bromo-2,4-Dimethoxypyrimidine in Drug and Agrochemical Innovation

    During the past decade, the importance of selectively substituted pyrimidines has grown. The 5-bromo-2,4-dimethoxy motif sits at a crossroads for synthetic teams wanting both diversification points and manageable deprotection chemistry. More drug candidates and new agrochemical leads now include these moieties—not by coincidence, but because structure-activity studies point again and again to their value.

    For example, when researchers attempt to install electron-withdrawing or bulky substituents on the pyrimidine ring, starting from this intermediate cuts steps compared to using less activated rings. The methoxy groups welcome demethylation or further derivatization under mild conditions, supporting rapid SAR cycles. In process chemistry, the compound's crystalline nature lends itself to straightforward isolation, facilitating robust scale-up.

    In recent years, biologists and formulation scientists have fed back that 5-Bromo-2,4-Dimethoxypyrimidine–derived scaffolds show improved bioavailability and metabolic stability in several cases. While we don’t make pharmacological claims, this recurring pattern among our clients illustrates why interest in the compound has only grown.

    Differences You Can See and Test: Not All Pyrimidines Are Equal

    It’s tempting to treat substituted pyrimidines as generic commodities. Our own work tells a different story. Small impurities, subtle differences in crystallinity, even trace mineral contaminants can complicate further syntheses. The original source, isolation method, and spectral confirmation are not academic exercises—they govern batch-to-batch performance. Unlike distributors or brokers, we watch the beginning and the end of the line.

    Some clients run side-by-side tests with samples from different sources. The typical findings: Our 5-Bromo-2,4-Dimethoxypyrimidine produces cleaner HPLC traces in coupled products and leaves fewer unknown spots in downstream analytical screens. These differences do not always show up on a spec sheet, but they save weeks in scale-up setbacks and failed regulatory submissions.

    Supporting Chemists at Every Step

    We have always valued open dialogue with our customers. Custom packing options, assistance with unusual delivery requirements, and on-demand technical support—these aren’t perks but standards set by the realities of fine chemical production. When a process engineer calls about slight color changes or unusual filtration profiles, our technical managers have likely seen the same challenge on the plant floor.

    As requests for 5-Bromo-2,4-Dimethoxypyrimidine grow, we invest further in analytical, application, and after-sales support infrastructure. Our in-house expertise isn’t limited to R&D chemists. Operations, supply chain managers, and quality professionals work together, closing the loop from process to product delivery.

    Making 5-Bromo-2,4-Dimethoxypyrimidine directly gives us a ground-level perspective. We see the results of small improvements or mistakes show up quickly in production output and customer satisfaction. Almost every process innovation—whether improved filtration, gentle drying, or advanced impurity tracking—emerges because working chemists and plant staff notice a point of friction and share ideas for improvement.

    Managing Supply and Reducing Downstream Delays

    One ongoing challenge in the industry is balancing unpredictable demand with steady, low-waste production. As a manufacturer, we hold running inventory and coordinate production batches to match forecasted projects, but the reality is that research projects and scaling timelines shift frequently. Our internal ordering systems stay connected to customers’ ongoing needs, aiming to prevent disruptions from shortages or overstocking.

    We also know that relying on traders or external brokers tends to expose chemists to longer wait times, outdated material, or inconsistent quality. Direct supply agreements, combined with transparent production schedules, help maintain the necessary buffer. By investing in real-time inventory systems, we provide faster, more accurate status updates, giving chemists greater control over their synthesis timelines.

    Solutions to Common Challenges with 5-Bromo-2,4-Dimethoxypyrimidine

    Every batch of 5-Bromo-2,4-Dimethoxypyrimidine travels a path from raw material through synthesis, purification, testing, packaging, to delivery. Along this path, we see recurring bottlenecks—contaminant carryover, loss during transfer, and rare but costly analytical outliers. Our in-house protocols have evolved to identify these pinch points early.

    Our technical support teams assist in troubleshooting reaction anomalies, such as incomplete couplings or stray peaks in product HPLC. Training both our people and our clients on best storage and handling practices pays off in fewer incidents and higher throughput. Investments in better containment and filtration have sharply reduced the occurrence of “off-spec” shipments.

    For new clients seeking to qualify or switch sources, we offer pilot lots and application support, helping them integrate our intermediate into their workflows with minimal disruption. New filtration and drying systems enable us to deliver higher-volume orders with shorter lead times and reduced batch-to-batch variability.

    Continuous Improvement Brings Us Closer to the Chemist’s Bench

    Not every step in the manufacture of 5-Bromo-2,4-Dimethoxypyrimidine is glamorous, but every optimization we implement—faster filtration, less solvent residue, a sharper NMR peak—shows up in the reliability and ease of use for our customers. Our technical managers regularly review user outcomes and coordinate with R&D chemists to anticipate new requirements, reagent compatibilities, or analytical protocols.

    Direct manufacturer-customer contact brings realities and possibilities together. We do not filter out complexity with scripted replies but work shoulder-to-shoulder with industrial chemists checking their first runs, or research groups evaluating a new library. The relationships built from hands-on support give us the insight to make the next process safer, cleaner, or more cost-effective.

    The Future for 5-Bromo-2,4-Dimethoxypyrimidine: Getting Ready for Tomorrow’s Projects

    The story of 5-Bromo-2,4-Dimethoxypyrimidine is not static. Ongoing advances in cross-coupling chemistry, greener catalytic methods, and automated synthesis platforms continue to elevate the relevance of reliable, well-characterized intermediates. Our manufacturing team remains committed to tailored support, quick response to changing regulatory landscapes, and continuous investment in both process and product data quality.

    End users don’t choose intermediates in isolation. They look for reliability, support, and evidence that their supplier knows the challenges of real synthesis. By focusing on direct production and open exchange of technical knowledge, we help chemists move from research idea to viable process, confident that their core intermediates won’t hold them back.

    What We’ve Learned and Where We’re Going

    Making and supplying 5-Bromo-2,4-Dimethoxypyrimidine has taken us through the entire spectrum of fine chemical production — from raw material sourcing to global delivery, from first kilo to ton-scale runs, from routine orders to troubleshooting on the chemistry front lines. Our path has always been shaped by feedback from working chemists and by lessons learned from batches that didn’t hit the mark.

    With each new partnership and every new request, we commit to better meeting the needs of scientists and engineers who depend on us for their success. Investing in process robustness, sustainable methods, and direct technical support, we ensure that our product continues to stand apart, supporting the creativity and progress of the chemical industry.