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2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid

    • Product Name 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid
    • Alias BBOPA
    • Einecs 暂无数据
    • 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

    345571

    Product Name 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid
    Cas Number 1021236-41-2
    Molecular Formula C19H17BN2O4
    Molecular Weight 348.16 g/mol
    Appearance White to off-white powder
    Purity Typically ≥95%
    Solubility Soluble in DMSO, DMF
    Storage Temperature 2-8°C
    Smiles B(C1=CN=C(OCc2ccccc2)N=C1OCc3ccccc3)(O)O

    As an accredited 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 1-gram quantity of 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid is securely sealed in a labeled amber glass vial.
    Shipping The chemical **2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid** is shipped in specialized, air-tight containers to ensure stability and prevent moisture exposure. Packaging complies with relevant chemical transport regulations, and the product is clearly labeled with hazard information. Temperature control may be implemented if required by the substance’s storage conditions.
    Storage 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid should be stored in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated environment. Keep it away from incompatible substances such as strong oxidizers. Recommended storage temperature is typically 2–8°C (refrigerator). Ensure proper labeling and follow institutional or manufacturer-specific safety guidelines for handling and storage.
    Application of 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid

    Applications of 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid in Industrial Manufacturing

    As a manufacturer expert in high-purity intermediates, we support pharmaceutical research, specialty chemical development, and advanced material innovation with 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid. Below we detail established, high-impact applications, each guided by industry regulations, controlled formulation guidelines, and real-world manufacturing practices for your technical evaluation.

    1. API (Active Pharmaceutical Ingredient) Intermediate Synthesis

    Major biotech and pharmaceutical firms rely on this compound as a boronic acid building block to introduce complex pyrimidine motifs during targeted drug synthesis. The reagent plays a critical role in Suzuki-Miyaura cross-coupling reactions, supporting the assembly of kinase inhibitors and other pyrimidine-containing APIs. Its reactivity enables efficient late-stage diversification under GMP-compliant conditions for both small-molecule drugs and investigational new molecular entities.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Current Good Manufacturing Practice (cGMP), US FDA 21 CFR Part 210/211
    • EU EudraLex Volume 4: GMP Guidelines for Medicinal Products
    • Japanese Pharmacopoeia (JP)

    Typical usage ratio

    • 0.2–1.0 mole equivalents per limiting reagent, adjusted based on substrate reactivity and target yield in the coupling step

    Downstream process integration

    • Enters as a protected pyrimidine coupling component after preliminary API core preparation; reacts under palladium catalysis in batch or continuous flow reactors

    Final product types

    • Small molecule kinase inhibitors (e.g., oncology drug candidates)
    • Central nervous system (CNS) agent intermediates
    • Pyrimidine-based anti-infective agents
    • Lead compounds for clinical trial supply

    2. Custom Synthesis for Agrochemical Actives

    Producers of modern crop protection agents utilize this boronic acid derivative as a specialized pyrimidine precursor for constructing novel herbicidal or pesticidal entities. Its compatibility with advanced palladium-catalyzed processes enables the integration of benzyloxy-protected features, conferring enhanced selectivity and environmental stability to downstream agrochemical scaffolds. Our technical support assists in scaling up pilot campaigns to commercial processes with regulatory transparency.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • FAO/WHO Food and Agriculture Organization Specifications for Pesticides
    • REACH Regulation (EC) No 1907/2006
    • China National Food Safety Standard—Maximum Residue Limits for Pesticides (GB2763)

    Typical usage ratio

    • 0.5–1.3 equivalents relative to halogenated aryl or heteroaryl partners, tailored according to scale-up yield efficiency

    Downstream process integration

    • Inserted at advanced intermediate stage of multi-step synthesis; typically serves as the nucleophilic partner in Suzuki coupling following functionalization of the base structure

    Final product types

    • Pyrimidine-based herbicide technicals
    • Fungicide active ingredient building blocks
    • Innovative insecticidal intermediates
    • Custom multi-target agrochemicals for registration dossiers

    3. Material Science: Organic Electronics and OLED Intermediate

    Research and manufacturing in organic electronic devices use this boronic acid for engineering electron-rich pyrimidine units within advanced organic semiconductors or light-emitting diode (OLED) materials. Its high purity and controlled benzyl protection deliver reliable results in constructing stable, high-mobility conjugated systems, supporting the scalability and reproducibility required for commercial optoelectronic device supply chains.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • IEC 62341-1-2: Display device reliability (for OLEDs)
    • RoHS Directive 2011/65/EU for hazardous substance restriction
    • Material-specific internal device QA/QC protocols

    Typical usage ratio

    • 0.8–1.2 equivalents in cross-coupling step, modulated for polymer length and device application

    Downstream process integration

    • Introduced at the pre-polymerization or direct arylation phase; reacts during monomer assembly before polymerization, or incorporated into precursor feedstock blends

    Final product types

    • OLED emitter layer pre-polymers
    • Organic photovoltaic (OPV) active layer materials
    • Pyrimidine-containing small-molecule semiconductors
    • Charge transport enhancer additives

    4. Advanced Chemical Research: Fragment-Based Drug Discovery Libraries

    CROs and drug discovery R&D labs implement this specialty pyrimidine boronic acid as a fragment for constructing focused screening libraries. The reagent enters boron-mediated coupling protocols to diversify core heterocycles, supporting structure–activity relationship (SAR) development with minimal protecting group interference. Our in-house quality systems ensure consistency at multi-gram to kilogram synthesis scales, facilitating reliable compound profiling.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for nonclinical sample preparation
    • ISO 17025:2017 Laboratory Accreditation (for analytical reproducibility)
    • Internal compound library documentation protocols
    • Applicable health and safety regulations: OSHA, EU CLP Regulation (EC) No 1272/2008

    Typical usage ratio

    • 1.0 equivalent per fragment coupling, often used in parallel synthesis formats to maximize library diversity

    Downstream process integration

    • Charges directly into library assembly plates for automated parallel or combinatorial syntheses; supports SAR exercise before scale-up

    Final product types

    • Fragment-based drug screening sets
    • Pyrimidine-focused medicinal chemistry tool compounds
    • Validated screening hits for early-phase lead optimization
    • Building block panels for hit-to-lead conversion

    5. Fine Chemical Synthesis: Specialty Ligand and Catalyst Manufacturing

    Specialty catalyst and ligand manufacturers select this compound to construct customized pyrimidine-inspired boron ligands for coordination chemistry and metal-mediated organic transformations. High batch reproducibility and minimized impurity profiles allow consistent scale-up in ligand design for custom catalysis, where trace metals and residual solvents must be rigorously controlled to meet downstream application needs.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • GHS/SDS chemical hazard communication protocols (EU REACH, OSHA)
    • Internal QC and trace metal analysis (ICP-MS/GC)
    • Nonpharmaceutical fine chemical supply regulations

    Typical usage ratio

    • 0.9–1.1 equivalents, closely matched to transition metal coupling or ligand backbone transfer to minimize waste and maximize yield

    Downstream process integration

    • Dosed into ligand precursor synthesis; engages in cross-coupling to furnish boron–pyrimidine cores, followed by deprotection and functionalization

    Final product types

    • Boron-modified homogeneous catalysts
    • Tailored N-heterocyclic ligand systems
    • Palladium or copper catalyst ancillary ligands
    • Organometallic research probes
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    Competitive 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    More Introduction

    2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid: A Chemist’s Perspective from the Floor

    Moving Past the Catalog: Why We Make 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid

    Long years standing by the reactors and stirring solutions shape a particular respect for molecules that actually get the job done. Working directly with 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid, we’re not simply filling demand or answering a market call. We’re building a reliable, high-purity intermediate that helps research chemists and process teams take concrete steps toward new pharmaceutical targets and advanced materials. This is not a “one-size-fits-all” boronic acid—our process for this compound bridges centimeter-scale innovation in the lab with the reality of multi-kilo production reliability.

    The Realities of Making It Right: Our Production Approach

    Sourcing boronic acids isn’t difficult, but ensuring the consistent quality of 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid requires more than a standardized protocol. We manufacture this molecule in controlled facilities where air and water quality tie directly into product outcome. Each batch goes through full traceability, and impurities don’t simply get noted for record-keeping—they push us to analyze every step, whether it’s the benzyl protection or the cross-coupling conditions.

    The model number we apply, internally, tracks synthesis iterations and purification runs. Over the years, our production chemists have seen how minor solvent impurities or temperature shifts during crystallization impact not just the yield, but the crystallinity and downstream performance. By the time a batch leaves our floor, we’ve seen the NMR, HPLC, and LC-MS profiles ourselves—not as a regulatory requirement but as a measure of our craft.

    Specifications That Reflect Chemistry, Not Just Standards

    We’ve chosen to focus on consistent purity and minimal moisture content for our 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid. Impurities under one percent don’t just mean a number on a certificate; they mean fewer headaches for project teams synthesizing complex targets. Low water content matters because boronic acids, especially those with protected aromatic rings, don’t behave the same when exposed to varying humidity. Over the years, we’ve replaced glassware and tweaked storage conditions simply to avoid hydrolysis or degradation that less attentive protocols can overlook.

    Each specification sheet we generate ties directly to the method used—our high-purity batches show clear, matched spectra that our customers can compare against their own controls. We’re not shipping unknowns. This is especially important for researchers trying to optimize Suzuki-Miyaura reactions or other transition metal-catalyzed couplings that show sensitivity to microimpurities.

    Practical Uses: Where Our Customers Take It

    Most of our production moves to pharmaceutical labs and advanced organic synthesis groups. Over the years, we’ve seen 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid used in scenarios where standard, off-the-shelf boronic acids either fail to couple efficiently or introduce side reactions. Customers working on kinase inhibitor scaffolds or constructing complex heterocycles prefer a product where the benzyloxy protections hold stable under the early stages of synthesis and deprotect cleanly when pushed by hydrogenation or stronger acids.

    One of the key factors that our partners talk about comes down to the purity required by medicinal chemistry teams. Even experienced project leads have recounted issues with trace byproducts from impure samples causing “ghost peaks” during analytic runs, wasting days of troubleshooting. Our attention to purity metrics directly supports clean, interpretable data. This goes beyond paperwork—the impact gets felt when a multi-step route doesn’t shut down due to failed coupling or unexpected chromatographic behavior.

    What Sets Our Product Apart

    There are competing products that claim good purity, but the real difference shows up in reaction performance. Having produced the molecule for several years, we have come to recognize the batch-to-batch consistency as the defining advantage. Teams accustomed to “mystery” boronic acids—products with variable purity or residual solvents—immediately notice tighter, more reproducible coupling yields with our material. Smoother isolation, simplified work-ups, and fewer chromatographic problems become not just theoretical selling points, but everyday benefits communicated to us by return customers.

    Another difference lies in how the benzyloxy groups behave. Over the years, we’ve seen competing samples where premature deprotection or partial hydrolysis led to poor yields or complicated downstream separation. In contrast, our internal stability data and real-world customer feedback confirm that our 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid retains integrity through a range of synthetic steps—this ultimately lowers the risk profile and labor involved in any drug discovery or development route.

    The Details Behind the Name

    Names can be overwhelming in synthetic chemistry. What matters most are the details tucked into the 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid molecule. Those benzyloxy protections are not afterthoughts; they fundamentally change how the pyrimidine ring interacts with reagents and solvents. Benzyl groups resist acidic conditions better than methyl or ethyl ethers and can be removed cleanly under hydrogenolysis—our experience shows this flexibility fits well into modular synthetic plans.

    Position five, where the boronic acid sits, offers the ideal anchor point for Suzuki couplings with aryl halides, especially where conjugation and planarity matter. We’ve seen our chemists succeed in coupling this building block into polycyclic backbones where less robust alternatives failed under similar conditions. The integrity of the boronic acid functional group stems from careful, stepwise synthesis, not from bulk commodity conversions or shortcut chemistry.

    Long-Term Reliability: Challenges and How We Address Them

    Boronic acids, generally, are not stable shelf-mates. Many labs have run into yellowing or resinous deposits developing in bottles shipped from careless suppliers. Our production team knows firsthand the frustrations and costs that come with lost batches and contaminated glassware. Over the past decade, we have invested heavily in new barriers, packaging, and post-production handling. Post-purification, the compound is sealed under dry nitrogen and stored in heavy-duty containers, not just to extend shelf life, but to make day-to-day lab use easier for our partners.

    Every batch includes clear, simple storage advice based on our own stability studies. We settled on low-oxygen, low-humidity environments after months of comparative trials that tracked discoloration, loss of boronic acid content, and build-up of degradation products. This is not just about shelf-life insurance—it gives chemists confidence that the material they use will behave the same on day one as it does after several months in inventory.

    Direct Feedback: Supporting Customers at Bench Level

    We have partnered directly with synthetic teams working in discovery chemistry, process optimization, and scale-up testing. Common themes emerge: frustration with highly variable boronic acids, difficulty with clean deprotection of benzyloxy groups, confusion with analytical artifacts from impurities. Rather than offering empty support promises, we have built a technical dialogue with researchers who use our 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid. This dialogue, in many cases, shapes our ongoing improvement cycles.

    Chemists bring us their failed coupling reactions or share spectra from their own labs. These experiences drive improvements in our synthetic routes, our quality control standards, and the technical documentation we supply. Stories of rescues, where a failed route gets resurrected by switching to our product, stay with us and push us to further tighten controls.

    Beyond the Reaction: Safety, Transparency, and Traceability

    Real chemical manufacturing never loses sight of user safety. Working directly with boronic acids, we train our production staff on how to handle pyrophoric byproducts, dust hazards, and exposure risks. Our attention to safety in synthesis translates into a safer experience for downstream users. We keep processes fully traceable, so customers always know which lot they are using and how to track its quality records. If a problem arises, we answer it openly, relying on actual batch data instead of stock explanations.

    Transparent processes and real-time feedback matter more to customers in active projects than generic promises of “quality.” We’ve seen that openness, plus willingness to share actual batch analytics, lets project teams run their own controls with confidence. This makes a tangible difference in high-value, time-sensitive research programs.

    Improving Year by Year: How Manufacturing Responds to Evolving Demand

    Research does not stand still. Over the years, demands for cleaner, more consistent boronic acids have grown. Teams working on structure-activity relationships, high-throughput screening, or custom medicinal probes do not want to second-guess their building blocks. By maintaining flexible manufacturing schedules and clear feedback loops, we support this diversity without sacrificing consistency.

    Emerging requests for larger volume batches or specialized purities sometimes challenge our capacity. Rather than stretching ourselves thin, we have built partnerships with trusted logistics and analytical labs. This collaborative approach helps us adapt, delivering material that stands up to complex synthetic needs.

    Comparing to Commodity Boronic Acids

    Several years in, we have watched the boronic acid market flooded with generic products. Many arrive from bulk syntheses with little attention to batch consistency. We have direct reports from labs that tried fast turnaround, low-cost substitutes, only to lose time fixing purity issues or troubleshooting multi-step syntheses that collapsed partway. The cost saved on material paled compared to the hours—sometimes days—lost on repeated purifications, failed couplings, or sorting out unknown side products.

    By focusing on reproducibility rather than cutting corners, we have filled a gap for teams that value reliable, predictable outcomes over marginal cost savings. Our approach pays off most clearly at scale, but our commitment stays the same for single-gram requests and multi-kilo shipments.

    Environmental Considerations in Modern Manufacturing

    Green chemistry is more than a slogan; pragmatic manufacturing faces growing pressure to minimize waste, adopt safer solvents, and improve process efficiency. Through years of process refinement, we have cut solvent usage by nearly a third compared to early protocols, and chosen work-up procedures that generate less acidic and basic waste. These improvements arose not only from external regulation but from working directly with chemical engineers who see the direct impact on reactor throughput and disposal costs.

    Improving sustainability, batch by batch, gives partners confidence that they are not inheriting hidden environmental liabilities. We have made a habit of sharing process improvements with research collaborators, so both process and R&D groups move forward together.

    Key Differences Observed from Direct Manufacturing

    Our collective experience points to several clear differences between our 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid and that from large-scale, automated suppliers. First, direct oversight of each run allows real-time reaction monitoring, reducing error rates and the risk of unknown byproducts. Second, in-house analytical teams operate alongside synthesis, not in isolation, so problems get caught early, well before product ships.

    This hands-on approach also improves response times for custom requests. If a customer’s synthetic route calls for a subtly different protection strategy or analytical format, we can adapt, discussing options with genuine chemists, not just sales staff.

    Looking Forward: Meeting the Needs of Advanced Research

    Pharmaceutical and material chemistry advances depend on trustworthy building blocks. Over the years, we’ve invested in robust feedback loops with process chemists, analytical experts, and logistics partners. These relationships deepen our expertise with each cycle. We encounter new synthetic challenges every quarter and respond by adjusting our protocols in step with the toughest project requirements in the field.

    We recognize that 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid is not a “mass market” commodity. Our efforts go toward supporting pioneers at the bench and production scale, who see the difference between a generic and a dedicated, manufacturer-produced quality. Every lot reflects years of learned adjustments, cumulative troubleshooting, and direct customer feedback. Every gram we ship stands as another step in a long partnership between manufacturer and innovator.