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2-Bromo-5-Nitropyrimidine

    • Product Name 2-Bromo-5-Nitropyrimidine
    • Alias 2-Bromo-5-nitro-pyrimidine
    • Einecs 607-757-0
    • 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

    836275

    Cas Number 4487-59-6
    Molecular Formula C4H2BrN3O2
    Molecular Weight 204.98
    Iupac Name 2-bromo-5-nitropyrimidine
    Appearance Yellow to orange solid
    Melting Point 120-124°C
    Solubility In Water Slightly soluble
    Density 1.96 g/cm3 (estimated)
    Smiles C1=C(N=C(N=C1Br)[N+](=O)[O-])
    Pubchem Cid 71592

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

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    Application of 2-Bromo-5-Nitropyrimidine

    Applications of 2-Bromo-5-Nitropyrimidine in Industrial Manufacturing

    As a manufacturer specializing in heterocyclic intermediates, we supply 2-Bromo-5-Nitropyrimidine to chemical producers developing advanced molecules for pharmaceuticals, agrochemicals, and specialty chemical sectors. Our customers employ this compound in highly specific downstream applications, integrating it in core synthesis steps that demand consistency, quality, and regulatory compliance. Below we detail the principal use cases supported by our manufacturing data, formulation insights, and customer feedback from real-world factories and labs.

    1. Pharmaceutical API Intermediate Synthesis

    Our customers in the pharmaceutical active pharmaceutical ingredient (API) sector use this pyrimidine derivative as an essential building block for synthesizing drug molecules, particularly kinase inhibitors, antiviral agents, and select oncology candidates. 2-Bromo-5-Nitropyrimidine acts as a halogenated intermediate, entering Suzuki, Buchwald–Hartwig, or nucleophilic substitution reactions to introduce unique pyrimidine cores, which remain critical in patent-protected API scaffolds. Clients require well-characterized raw material for achieving defined impurity profiles and consistent batch-to-batch results in cGMP environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP monographs for related pyrimidine-based APIs
    • European Pharmacopoeia (Ph. Eur.) relevant general chapters
    • FDA 21 CFR Part 211 (Applicable to finished drugs integrating intermediates)

    Typical usage ratio

    • Typically 1.1–1.5 molar equivalents per reaction step, adjusted according to excess requirements and yield optimization during key coupling or substitution steps. The precise ratio will vary based on the API target and catalytic system.

    Downstream process integration

    • Material is introduced early in multistep synthesis, usually during the heteroaryl coupling or halogen displacement phase, before final deprotection and salt formation steps for finished APIs.

    Final product types

    • Small molecule oncology APIs (e.g., kinase inhibitors)
    • Antiviral pharmaceutical products
    • Research-grade pyrimidine analogues

    2. Agrochemical Active Ingredient Synthesis

    Manufacturers of crop protection agents and plant growth regulators select this compound for assembling pyrimidine-ring-containing herbicides, fungicides, and insecticides. The bromo and nitro functionalities allow for controlled introduction of reactivity during selective cross-coupling or nucleophilic aromatic substitution, producing target molecules with precise substituent patterns to meet global registration requirements. Reliable quality and trace contaminants monitoring align with regulatory dossiers submitted to agricultural authorities.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD guidelines for chemical impurities and analytical methods (e.g., OECD 107/117/405)
    • REACH (EU) Regulation (EC) No 1907/2006
    • China GB 2763 (Maximum Residue Limits for Pesticides)

    Typical usage ratio

    • 0.8–1.3 molar equivalents per intermediate synthesis depending on targeted crop protection molecule and expected coupling yield. Process engineers adjust the amount to minimize by-product formation and maximize isolated yields.

    Downstream process integration

    • Fed into multi-stage syntheses, normally during early introduction of the pyrimidine core, then further modified by cross-coupling or acylation to obtain the active ingredient before formulation into AI concentrates or mixed formulations.

    Final product types

    • Selective herbicides based on pyrimidinyl scaffolds
    • Pyrimidine-based fungicides for cereals and fruits
    • Plant growth regulators and insecticidal compounds

    3. Electronic Chemical Intermediate for OLED Materials

    Producers in the organic electronics field incorporate this pyrimidine intermediate when engineering hole-transport and electron-transport materials for next-generation organic light-emitting diodes (OLEDs). The dual presence of nitro and bromo groups facilitates stepwise substitution, offering an avenue to obtain highly pure, functionalized pyrimidines for use in electroluminescent layers. Stringent quality control enables integration with electronics-grade standards and low ionic contaminant requirements demanded by display manufacturers.

    Industry compliance standards

    • ISO 9001:2015 for quality management in advanced materials
    • IEC 60068-2 environmental and purity standards for electronic chemicals
    • RoHS Directive (2011/65/EU) for restricted substances
    • Customer-specific electronics-grade metal impurity limits (often <10 ppm)

    Typical usage ratio

    • 0.9–1.2 equivalents per pyrimidine-linking reaction in small molecule OLED precursor syntheses, adjusted based on the degree of functionalization and downstream layer purity specifications.

    Downstream process integration

    • Undergoes Buchwald–Hartwig or similar cross-coupling as the primary heterocyclic input for subsequent derivatization, prior to functionalization, purification, and thin film processing for electrode-compatible intermediates.

    Final product types

    • Electron-transport and hole-transport layers for OLED modules
    • Emitter precursors for organic display pixels
    • Pyrimidine-linker molecules in high-performance organic semiconductors

    4. Specialty Fine Chemical Intermediate for Dye Manufacturing

    Dye manufacturers engaged in specialty textile, photographic, and analytical colorants utilize this intermediate to introduce heterocyclic nuclei with color-tuning substituents. Pyrimidine-based dyes offer enhanced fastness and unique absorption profiles essential in high-performance textile and technical dye segments. The compound’s controlled halogenation and nitration permit direct coupling into azo, anthraquinone, or other heterocyclic dye series where structural identity and minimal batch variation are critical.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for restricted substances in textile dyes)
    • Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH, EU)
    • EN 71-3 (Toys Safety—migration of certain elements, relevant for dyes in children’s textiles)
    • ISO 14001 (Environmental Management for chemical manufacturing)

    Typical usage ratio

    • Wide range, often 1.0–1.4 equivalents relative to coupling partner, depending on the dye system (azo, anthraquinone, or pyrimidine backbone) and required tinctorial strength; final ratio defined by chromatographic purity and batch yield.

    Downstream process integration

    • Introduced as an electrophilic partner for nucleophilic aromatic substitution or diazo coupling early in dye backbone assembly, followed by derivatization and sulfonation, then purification to textile or analytical grade.

    Final product types

    • High-washfast textile dyes for polyester and nylon
    • Pyrimidine-based colorants for inkjet and photographic applications
    • Specialty dyes for laboratory diagnostic reagents
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    Certification & Compliance
    More Introduction

    2-Bromo-5-Nitropyrimidine: A Reliable Building Block for Modern Synthesis

    Discovering the Value of 2-Bromo-5-Nitropyrimidine

    In the world of fine chemicals, some compounds quietly carry a lot of weight behind the scenes. 2-Bromo-5-nitropyrimidine stands out in that way. This molecule fits into a wide range of advanced research and manufacturing efforts. For those working with heterocyclic chemistries, it frequently shows up as a handy intermediate that fosters progress across several fields. I remember the first time I handled a batch in the lab; it was for a side-chain introduction on a pyrimidine ring system that seemed nearly impossible until this exact structure came into play.

    Specs That Matter in Real-World Applications

    2-Bromo-5-nitropyrimidine arrives as an off-white to pale yellow crystal, with a molecular formula of C4H2BrN3O2 and a molar mass around 219.99 g/mol. What instantly makes it attractive is its combination of two robust functional groups: bromine and nitro. Both offer unique reactivity that opens doors to various synthetic steps, especially those involving nucleophilic substitution or cross-coupling techniques. Purity levels commonly meet the demands of high-stakes pharmaceutical and material synthesis. Purity influences how clean your reactions run, and that matters a lot to yield and reproducibility. I've witnessed batches where a few decimal points in purity led to hours lost in side-product cleanup—a difference you feel when racing against project timelines.

    The melting point, usually clocking in above 150°C, gives some peace of mind for storage and handling in most lab environments. Sensitivity to moisture is minimal, but I always keep it capped tight due to the reactive bromine—better safe than sorry, especially with compounds that spend months on the shelf.

    Usage in Research – Direct and Indirect Benefits

    2-Bromo-5-nitropyrimidine doesn’t ride in the limelight, but folks in medicinal chemistry, agrochemical development, and dye research have stories to share about its utility. Its pyrimidine core makes a sturdy backbone when you’re preparing analogs of biologically active molecules, especially kinase inhibitors or potential antivirals. With the bromine at the two position and the nitro group at five, chemists use it in modular syntheses—swapping the bromo for amines, thiols, or carbon-based nucleophiles; tweaking the nitro group to include more functionality by reduction or other transformations.

    The Suzuki and Buchwald-Hartwig couplings thrive with the bromo leaving group here; anyone who’s tried to coax reactivity from a less accommodating halide on a similar ring will immediately notice the difference. Sometimes, a tricky step that would stall out with chloro or iodo analogs suddenly clicks when you bring 2-bromo-5-nitropyrimidine into the mix. It’s less about theoretical advantage and more about real reactions running with less effort, especially in iterative library production.

    How It Compares: Finding the Right Fit Among Pyrimidine Intermediates

    For anyone knee-deep in synthetic planning, the choice between halogenated pyrimidines and their nitro counterparts comes down to both yield and pathway flexibility. Take 2-chloro-5-nitropyrimidine, which pops up in catalogues as a close cousin. Despite apparent similarities, the bromo version brings superior reactivity under many conditions. There’s less forcing needed—temperatures can be lower, and the selectivity often stays sharper. In my years working with both, I rarely reach for the chloro variant unless specifically called for by downstream compatibilities. While the iodo derivative might beat out the bromo for bulkier couplings, the price jump and instability on extended storage can make it a less attractive workhorse for day-to-day runs.

    Comparing it to pyrimidines minus the nitro, the difference becomes even starker. The electron-withdrawing effect from nitro makes the ring more open to substitution, especially on adjacent carbons. For colleagues pushing targets that call for quick derivatization or late-stage modifications, this can flatten learning curves and help scale new synthesis ideas without endless troubleshooting. Skipping those headache-inducing reruns means more time spent getting to the actual science rather than redrawing routes.

    Addressing Production and Environmental Questions

    Every synthetic chemist asks about costs—and not just in dollars. 2-Bromo-5-nitropyrimidine doesn’t escape scrutiny over its track record when it comes to manufacturing waste and safety protection. The pathway to its preparation involves bromination and nitration, sometimes requiring robust controls and responsible effluent handling. Modern procedures lean heavily on greener chemistry, minimizing hazardous byproducts as much as technically possible. I’ve toured facilities that caught up quickly, switching to selective oxidants and improved filtration, which kept both yields up and regulatory headaches down.

    Working in a lab makes you realize that safe, contained bromination beats wild, uncontrolled reactions every time. There’s always room for better waste treatment onsite—including real-time halide recovery or closed-loop solvent systems. As someone who’s steered a handful of pilot batches, those investments make the difference between a reliable supply and a regulatory bottleneck. It also builds greater trust with teams concerned about occupational exposure, since nobody wants to gamble on inhaling halogenated fumes day after day.

    The Role in Scale-Up and Industry Solutions

    Labs use milligram and gram amounts, but industry talks in kilos and metric tons. Scale-up brings its own brand of challenges: batch homogeneity, heat management, and supply chain consistency become the hot topics. 2-Bromo-5-nitropyrimidine holds up well under these tests—consistent crystallinity, good shelf stability, and reliable performance over multiple lots. Suppliers who optimize process parameters, calibrate storage conditions, and maintain tight handling protocols earn a strong market reputation. It’s not just about getting a drum at a good price; it’s about knowing that last drum will behave just like the first one, month after month.

    One persistent friction point involves global logistics, since halogenated intermediates sometimes run afoul of customs in certain jurisdictions. Maintaining clear, traceable documentation streamlines clearance, and regular supply chain audits keep disruptions to a minimum. A supplier that works closely with logistics experts smooths these bumps before they become costly delays for end users.

    Meeting Safety and Compliance Standards

    Safety officers scrutinizing chemical supplies pay special attention to compounds like 2-bromo-5-nitropyrimidine for their bromine and nitro content. The safety profile requires transparent communication about hazards and respect for regulations covering storage, handling, and labelling. I know the relief of unpacking a shipment that arrives with crystal-clear instructions and up-to-date documentation. You notice the difference right away in workflow efficiency and risk reduction. Good vendors supply detailed safety data, minimizing guesswork and preventing unnecessary exposure.

    Using appropriate PPE and ensuring proper ventilation go a long way in preventing accidents. Experienced teams know how to negotiate the balance between urgency and safety, preparing fresh solutions only when needed and keeping stocks in properly labeled secondary containers. Clear training and routine checks reinforce safe habits, and reduce emergency interventions to a bare minimum. Regular reviews of spill protocols and waste disposal mean the lab stays a place for progress, not a source of avoidable incidents.

    Supporting Diverse Fields: Pharmaceuticals and Beyond

    Pharmaceutical discovery drives demand for clean, responsive intermediates. 2-Bromo-5-nitropyrimidine’s reactivity profile lines up well with needs for rapid analog synthesis, especially when time-to-candidate can dictate the fate of whole projects. In my experience, its use in kinase inhibitor research stands out. One popular approach builds on the scaffold with palladium-catalyzed cross-coupling, customizing side chains for greater potency or metabolic stability. The reliable response of the bromo leaving group lets teams iterate fast without the usual headaches of sluggish conversions.

    Agrochemical syntheses borrow from similar logic, adapting the pyrimidine framework for herbicide or pesticide leads. Here, speed and purity again matter. Missing a beat means costly development timelines or regulatory hurdles, but this compound works smoothly in multi-step setups. Dye chemistry and advanced materials—fields that traditionally face barriers from inconsistent or weakly reactive intermediates—also benefit from the robust platform it provides. The ability to customize substituents and bypass harsh conditions increases design freedom, opening new product categories that weren’t feasible before.

    Pushing for Better Practices: Efficiency and Green Chemistry

    A key topic among both researchers and commercial users now focuses on improving sustainability. Sourcing greener starting materials, recycling solvents, and designing less wasteful synthesis pathways matter more than ever. I’ve seen groups successfully introduce catalytic protocols for both nitration and bromination, slashing raw material excess and reducing secondary pollution. It’s not simply about pleasing auditors—it’s about minimizing headaches and costs from hazardous waste and ventilation management.

    Cross-disciplinary collaboration can push these initiatives further. Chemists, production engineers, and environmental experts working together find efficiencies—think in-line monitoring for reaction progress, advanced purification technologies, and on-site neutralization systems for acidic and basic waste. Making improvements permanent means tying them directly to production metrics like cost-per-kilo and batch-to-batch reproducibility. Small changes, like switching to semi-continuous processes or integrating microreactors for critical steps, show up as lower utilities bills and smoother scale-ups. The more these lessons travel through the community, the better for everyone relying on intermediates like 2-bromo-5-nitropyrimidine.

    Handling and Storage Lessons from Real-World Labs

    Having spent years with variously sensitive chemicals, good storage habits stand out as underrated. 2-Bromo-5-nitropyrimidine tolerates routine lab storage quite well, avoiding troublesome decomposition as long as containers remain well sealed and protected from extremes. In my lab, storing it alongside other stable, low-volatility intermediates kept contamination events to almost zero. Air exposure rarely causes immediate problems, but learning from the rare “what if” moments sharpens everyone’s discipline—residual water from carelessness can encourage minor side reactions that cloud final purity, which you won’t catch until much later.

    Labeling all containers, recording batch numbers, and keeping a simple usage log saved far more time than ever spent cataloguing. For larger-scale facilities, strict rotation of inventory ensures older batches serve before shelf life becomes questionable. Automated weighing and dispensing eliminate guesswork, so you waste less and can document every transfer for eventual audits or troubleshooting.

    Skyrocketing Demand: Market and Supply Chain Insights

    Growth in both new drug discovery and novel agrochemicals keeps demand for 2-bromo-5-nitropyrimidine high. Supply disruptions can tank entire syntheses, so reliability matters as much as price. Sourcing from partners with proven records and up-to-date compliance certifications shields teams from the headaches of lost batches or regulatory snags. I’ve dealt with both direct and indirect suppliers, and those who invest in robust quality management consistently smooth out problems before they ever reach the end-user.

    Diversifying supply sources, sharing clear planning forecasts, and leaning on digital inventory management help keep projects running smoothly. During the pandemic, I saw firsthand how pre-existing partnerships kept shipments coming. Without that preparation, many would have faced months-long delays. Having a backup plan for critical intermediates sits right alongside everything else in a project risk register—experienced teams never treat this lightly.

    Choosing 2-Bromo-5-Nitropyrimidine: What Informed Researchers Value

    In discussions with colleagues and mentors across various sectors, a few themes stand out when selecting a core heterocycle for flexible synthesis. Predictability, high conversion rates, and product purity regularly top the list. 2-Bromo-5-nitropyrimidine always enters those conversations because it delivers on these points. Longtime users recall fewer clogged reactors, cleaner work-ups, and less time spent sorting byproducts when this compound takes center stage in synthesis.

    An ability to swap out base or catalyst without catastrophic fallout attracts both risk-averse and innovation-driven researchers alike. Many let their experience guide choice of palladium or copper cross-couplings, then adjust parameters as conditions demand. The forgiving nature of the bromopyrimidine core accommodates a fair dose of creativity, enabling both classic approaches and novel adaptations. Teams repeatedly return to it for rapid hit-to-lead programs, not only for its chemical qualities but because of fewer setbacks during execution.

    Innovation and Continuous Improvement

    Research doesn’t stand still. New reactions, improved ligands, and better reagents pop up every year. 2-Bromo-5-nitropyrimidine slots neatly into these evolving frameworks. Recent trends favor more selective activation, whether through photochemistry, electrochemistry, or designer catalysts. Early results hint at both lower energy usage and fewer side reactions. In practical settings, a chemist who embraces these innovations can hit tighter targets, both in product yield and sustainability.

    I’ve watched several teams adapt flow chemistry approaches to couple 2-bromo-5-nitropyrimidine continuously, sidestepping problems with heat or mass transfer that plague older, batch-based operations. These tweaks allow finer control, reduce batch-to-batch variability, and sometimes even cut costs. Teams able to pilot improvements quickly gain advantages—faster iterative testing, more robust scale-up, better reproducibility. Translating lessons from small-scale exploratory work into large-scale commercial runs builds long-term value for any business tied to chemistry innovation.

    Facing Common Obstacles and Finding Real Solutions

    No intermediate solves every challenge. Handling is usually the least of anyone’s worries, but occasional sticking points do arise. Sometimes, reactivity runs too high, chewing through sensitive substituents. Other times, impurities sneak in from upstream batches, complicating troubleshooting. Open and honest data-sharing between purchasers and producers helps head off frustration. I recall one project where a tough impurity profile threatened our timelines, but a frank conversation with a supplier uncovered a tweak in their recrystallization steps. The next shipment sailed through QC checks without a hitch.

    User communities sharing experiences—good or bad—help build a bank of institutional wisdom. Collective solutions pop up faster when labs document both strong and weak runs, circulate feedback, and push for incremental changes when needed. Investing in a strong relationship with your supplier can turn up early warnings before problems snowball. Producers willing to respond quickly, investigate complaints, and tweak batches based on customer data keep their clients happier—and their reputation solid.

    Looking Forward: The Lasting Importance of Smart Chemical Choices

    Chemistry, at its core, rewards reliable tools just as much as brilliant innovation. 2-Bromo-5-nitropyrimidine endures because it quietly shortens the gap between inspiration and verification. In labs around the world, it helps researchers push out new lead compounds, streamline agrochemical candidates, and develop smarter materials. Its specific mix of reactivity and stability, combined with real-world value demonstrated through years of dependable performance, ensures its continued presence on lab benches and in kilolab facilities.

    Long-term users will keep pushing for safer, greener, and smarter processes. Everyone wins when suppliers, handlers, and end-users learn together and pass forward better practices. My time with 2-bromo-5-nitropyrimidine taught me that real innovation doesn’t always scream for attention; often, it’s the reliable, robust choices that stay relevant year after year, fueling both progress and discovery.