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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 | 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. |
Applications of 2,4-Bis(Benzyloxy)Pyrimidine-5-Boronic Acid in Industrial ManufacturingAs 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 SynthesisMajor 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
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2. Custom Synthesis for Agrochemical ActivesProducers 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
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3. Material Science: Organic Electronics and OLED IntermediateResearch 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
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4. Advanced Chemical Research: Fragment-Based Drug Discovery LibrariesCROs 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
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5. Fine Chemical Synthesis: Specialty Ligand and Catalyst ManufacturingSpecialty 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
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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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.