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3-Amino-5-Bromo-2-Fluoropyrimidine

    • Product Name 3-Amino-5-Bromo-2-Fluoropyrimidine
    • Alias 3-Amino-5-bromo-2-fluoropyrimidine
    • Einecs 821-725-2
    • 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
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    Specifications

    HS Code

    644669

    Product Name 3-Amino-5-Bromo-2-Fluoropyrimidine
    Cas Number 943114-83-2
    Molecular Formula C4H3BrFN3
    Molecular Weight 191.99 g/mol
    Appearance White to off-white solid
    Melting Point 75-79°C
    Solubility Soluble in DMSO, slightly soluble in water
    Purity Typically >98%
    Storage Temperature 2-8°C (refrigerated)
    Smiles C1=C(C(=NC(=N1)N)F)Br
    Inchi InChI=1S/C4H3BrFN3/c5-2-1-8-4(7)9-3(2)6/h1H,(H2,7,8,9)
    Synonyms 5-Bromo-2-fluoropyrimidin-3-amine

    As an accredited 3-Amino-5-Bromo-2-Fluoropyrimidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 3-Amino-5-Bromo-2-Fluoropyrimidine

    Applications of 3-Amino-5-Bromo-2-Fluoropyrimidine in Industrial Manufacturing

    As an experienced producer of 3-Amino-5-Bromo-2-Fluoropyrimidine, we supply this high-purity intermediate to major synthesis-driven industries. Downstream manufacturers depend on its controlled reactivity and selective substitution pattern for advanced heterocyclic compound development. Each application scenario below highlights real, large-scale uses, specifying compliance protocols, applied dosage levels, process integration, and typical end products by sector.

    1. Pharmaceutical API Intermediate Synthesis

    This raw material functions as a critical building block in the multi-step synthesis of active pharmaceutical ingredient (API) precursors, including new-generation pyrimidine-based antiviral and anticancer drugs. Medicinal chemists exploit its site-selective amino and halogen groups to assemble complex scaffolds in regulated cGMP facilities, following highly scrutinized process controls. Downstream users specifically adjust reaction conditions to maximize yield and minimize byproducts for active units ultimately formulated into finished tablets or injectable agents.

    Industry compliance standards

    • ICH Q7 GMP Guidelines for APIs
    • US FDA 21 CFR Part 210/211
    • EU GMP Directive 2003/94/EC
    • USP/NF and EP Monograph requirements for starting material traceability

    Typical usage ratio

    • Ranged at 0.01–0.3 molar equivalents relative to pyrimidine framework, tuned according to batch size and API yield optimization studies

    Downstream process integration

    • Introduced at the heterocycle assembly stage or as a key precursor feedstock for nucleophilic aromatic substitution or amidation, upstream of purification/ crystallization unit operations

    Final product types

    • Small molecule oncology drug APIs
    • Antiviral nucleoside analog precursors
    • Pharmaceutical research intermediates
    • Finished prescription tablet or injectable formulations

    2. Agrochemical Active Ingredient Synthesis

    Pyrimidine-substituted scaffolds produced from this intermediate are central to developing new fungicide and herbicide active ingredients. Agrochemical R&D centers deploy this raw material in route scouting for active units exhibiting selective crop protection profiles. Synthesis routes require tightly monitored reactant ratios and batch records to meet global crop safety standards. The downstream integration ensures synthesis of high-purity agrochemical actives that withstand residue and environmental target restrictions.

    Industry compliance standards

    • FAO/WHO JMPR pesticide specification guidelines
    • EPA FIFRA registration criteria
    • ISO 9001:2015 for quality consistency
    • REACH Annex VII registration for supply chain transparency

    Typical usage ratio

    • Typically 5–20% by mol of total active scaffold feed reaction, dependent on functionalization steps and desired herbicide or fungicide performance

    Downstream process integration

    • Fed into the heterocycle formation sequence on automated pilot and production scales, preceding final acylation or sulfonation for pesticide actives

    Final product types

    • Pyrimidine-derived fungicides
    • Selective herbicide technical concentrates
    • Crop protection active ingredient isolates
    • Formulated suspension concentrates (SCs)

    3. Veterinary Drug Intermediate Production

    This compound serves as a highly specific precursor for veterinary medicine synthesis, particularly in the preparation of antiviral and antiparasitic drugs for animal health applications. Its precise fluorinated and brominated substitution permits targeted modification, streamlining downstream derivatization and purification stages. Veterinary formulators must document impurity profiles and proven batch homogeneity to comply with animal safety and residue regulations. This intermediate is favored in production lines requiring reliable scale-up data for subsequent registration.

    Industry compliance standards

    • VICH GL2 cGMP for veterinary pharmaceutical manufacture
    • EU Regulation 2019/6 on veterinary medicinal products
    • US FDA Guidance for Industry #63
    • ISO/IEC 17025 analytical validation for residue testing

    Typical usage ratio

    • Used at 0.05–0.25 molar ratios based on pharmacophore yield targets and impurity minimization protocols

    Downstream process integration

    • Added at the nucleophilic substitution step or functionalization phase preceding coupling with bioactive side chains and final crystallization

    Final product types

    • Veterinary antiviral API intermediates
    • Antiparasitic drug intermediates for livestock and companion animals
    • Active veterinary ingredient formulations for injection
    • Premix compounds for mineral-blend supplements

    4. Specialty Dye and Pigment Synthesis

    Custom dye manufacturers utilize this intermediate to access pyrimidine-derived motifs in high-performance colorant chemistry, particularly for electronic imaging, inkjet pigment, and photoreactive dye matrices. Synthesis at this level demands rigorous documentation of halogen and amine content for both purity and stability in final pigment dispersions. QC teams rely on spectroscopic fingerprinting and batchwise chain-of-custody for color fastness requirements in regulated sectors such as textile and digital printing.

    Industry compliance standards

    • Oeko-Tex Standard 100 for textile dye applications
    • REACH (EC) No. 1907/2006 for pigment registration
    • EN 71-3:2019 for toy/colorant safety
    • ISO 9001:2015 for manufacturing quality

    Typical usage ratio

    • Introduced at 2–8% by weight of total monomer feed for pigment backbone synthesis, with adjustment based on chromophore yield and spectral performance

    Downstream process integration

    • Employed in the early heterocyclic core formation and subsequent halogenation/amination steps ahead of pigment dispersion protocols

    Final product types

    • Reactive dyes for inkjet and laser imaging
    • Pigments in photonic paints for electronic display manufacturing
    • High-stability textile dye batches
    • Engineering plastics colorant masterbatches

    5. Electronic Materials Intermediate

    Advanced electronics manufacturers integrate this compound into molecular precursor design for organic semiconductors and electronic display components. Process engineers employ it where fluorinated pyrimidine motifs can enhance charge mobility and stability within organic field-effect transistors (OFETs) and OLEDs. Strict materials traceability and controlled reaction atmospheres are essential for achieving reproducible electronic performance in final components supplied to device assembly lines.

    Industry compliance standards

    • IEC 60086 and IEC 62321 for electronics material content
    • IPC-5703 for surface contamination control
    • RoHS 2011/65/EU for hazardous substance limitations
    • ISO 14001:2015 for environmental management during synthesis

    Typical usage ratio

    • Applied at 0.5–5% by mol in monomer precursor synthesis, adjusted by device structure and conductivity requirements

    Downstream process integration

    • Added at conjugated core assembly step prior to high-purity distillation and formulation for device-grade intermediate supply

    Final product types

    • Organic semiconductor intermediates for OFETs
    • Molecular building blocks for OLED display manufacture
    • Precursor chemicals for printed electronic circuitry
    • Photoactive layers in flexible electronic films
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    More Introduction

    3-Amino-5-Bromo-2-Fluoropyrimidine: A Closer Look

    Introduction to a Specialized Pyrimidine Compound

    Chemistry often feels abstract until a compound pops up that sparks curiosity and delivers real practical value. 3-Amino-5-Bromo-2-Fluoropyrimidine does exactly that for anyone working in synthesis, especially in the world of pharmaceuticals or advanced material research. Pyrimidine structures occur everywhere in biochemistry — even DNA and RNA rely on pyrimidine rings as foundational elements. Swapping even one atom on that ring can lead to new properties and unlock different pathways in laboratory synthesis. Here, the addition of amino, bromo, and fluoro groups creates a molecule with both stability and reactive handles, something I appreciate after running into too many dead ends with less versatile compounds.

    What Sets This Compound Apart

    Switching from pure speculation to hands-on use, the first thing anyone notices with 3-Amino-5-Bromo-2-Fluoropyrimidine lies in the trio of modifications on the core ring. The amino group at position 3 opens doors to nucleophilic reactions, which I often capitalize on for connecting new fragments or creating building blocks. The bromo group at position 5 simplifies cross-coupling reactions. When building libraries for small-molecule drug discovery, that bromine saves steps. The fluoride at position 2 changes the electronic landscape in subtle ways, impacting hydrogen bonding and lipophilicity — two big factors in medicinal chemistry.

    While other pyrimidine derivatives might include just a halogen or amino group, this compound’s single arrangement lets it step in as a starting material where selectivity and reactivity matter most. I’ve seen labs beat their heads against inert analogues with less switching flexibility, struggling to install functional groups after the fact. In contrast, this molecule offers clear points for modification, reducing wasted effort.

    Specifications and Purity: What Matters in Practice

    Purity ranks as a deciding factor every time I pick a reagent for a sensitive synthesis. Reliable sources ensure this compound typically comes at over 98% purity, often presented as a white to off-white crystalline powder. That might sound dry, but it means one less variable to worry about in the reaction flask. Consistency in melting point and a narrow range also reflect solid batch control.

    Plenty of folks overlook the impact of even trace impurities — not just on yield but on the formation of hard-to-separate side products that haunt isolation steps. Once, trying to scale from milligram to gram quantities, impurity in a similar halogenated pyrimidine ruined not just one batch but set back an entire project. Having access to high-quality 3-Amino-5-Bromo-2-Fluoropyrimidine keeps both time and budget on track.

    Real-World Uses: From Synthesis to Small-Molecule Work

    Going beyond the catalog page, this compound finds practical use as an intermediate in pharmaceutical research, crop-protection chemistry, materials development, and dye synthesis. In my own projects, I’ve reached for this molecule when planning Suzuki-Miyaura couplings to add aryl groups, or Buchwald-Hartwig reactions to extend heterocycles. The arrangement of substituents supports regioselectivity — a relief compared to less functionalized pyrimidines, which sometimes give messy mixtures and headaches at the purification stage.

    Small changes at the atomic level can reshape biological activity in profound ways. Medicinal chemists often need heterocycles that blend lipophilicity, hydrogen bonding, and unique shapes. This compound, because of its halogen and amino pattern, often gives the right profile for further development. I’ve seen it help produce kinase inhibitors or anti-viral leads, letting teams move swiftly to new analogues just by using the built-in functional groups.

    Not every laboratory has the budget for a vast chemical library. Having a compound like 3-Amino-5-Bromo-2-Fluoropyrimidine as a flexible starting point lets labs stretch limited resources and explore new targets, rather than getting boxed in by more rigid compounds.

    Comparing with Other Pyrimidine Derivatives

    Drawing a line between 3-Amino-5-Bromo-2-Fluoropyrimidine and standard pyrimidine shows clear distinctions. Many classic building blocks feature only one functional group, like 2-chloropyrimidine or 5-bromopyrimidine. Each offers reactivity, but in isolation, they limit the paths for later modification. Tossing all three groups onto the same ring at these positions immediately multiplies options for a synthetic chemist. I remember comparing yield and complexity between a mono-substituted pyrimidine and this variant — the difference in downstream flexibility became obvious long before workup and purification.

    In some ways, this compound becomes a “Swiss army knife” for ring modifications. Others in the same chemical family — like 2,4,6-trisubstituted pyrimidines — tend to restrict substitution patterns or demand harsher conditions to react effectively. 3-Amino-5-Bromo-2-Fluoropyrimidine sits at a midpoint: reactive enough for most useful transformations, but stable enough to handle purification and storage without breakdown. That blend rarely shows up in similar reagents.

    Handling and Safety from Hands-On Experience

    Long hours in the lab drill safety concerns deep into your habits. While 3-Amino-5-Bromo-2-Fluoropyrimidine does not top typical hazard lists, gloves, goggles, and a sash down on the fume hood remain common sense. Washing up after any handling prevents unexpected skin contact, particularly because halogenated heterocycles sometimes irritate sensitive skin. Like most fine chemicals, protecting it from moisture and letting the lid snap tight post-measurement keeps it fresh for repeat syntheses.

    I keep a habit of labeling, double-sealing, and tracking even when the risk seems low. Knowing exactly what's in the jar avoids any casual mix-up, which especially matters when several derivatives sit near each other on the supply shelf. In practice, accidents rarely happen with careful method, but it takes just one bad day to wish for stricter discipline.

    Supply Chain, Traceability, and Responsible Sourcing

    Supply reliability carries weight, especially if working at scale. Sourcing from suppliers who publish batch COAs (Certificates of Analysis) brings peace of mind. Back in 2020, a shortage of high-quality heterocycles slowed down timelines on crucial projects, a sobering reminder that global logistics and reputable sources should never be taken for granted. Traceability connects to the heart of E-E-A-T: expertise and trust come not just from technical know-how, but from clear handling of sourcing, quality control, and documentation.

    Most trustworthy suppliers now use chromatography and NMR to guarantee every lot — details that matter if purity or trace side products can affect downstream biological testing. Labs with strict regulatory or IP requirements rely on this traceability when filing patents or publishing data. Getting burned on poorly documented chemicals once convinced me to always ask for that extra paperwork.

    Cost Considerations and Long-Term Value

    Budget constraints frequently steer choices in research. 3-Amino-5-Bromo-2-Fluoropyrimidine sits in a mid-range price bracket; not always the cheapest, but reasonable for its utility and flexibility. Cheap analogues sometimes hide nasty surprises like residual heavy metals or moisture-sensitive impurities. Spending a bit more on reliable material avoids the cycle of troubleshooting mystery results.

    Switching out to an alternative often means reworking protocols and rediscovering solvent preferences, temperatures, and reaction times. In my own work, standardizing on one high-purity intermediate helps recover cost through fewer failed experiments and less time wasted on repeat purifications. For teams working under tight deadlines, that stability pays for itself quickly.

    Building Innovation from Accessible Chemistry

    Lab work rewards those who can improvise and adapt, rather than fall back on routine choices. 3-Amino-5-Bromo-2-Fluoropyrimidine opens creative doors. Designing a new synthesis without the right functional handles always leads to complicated detours — extra protection/deprotection steps or workaround functionalizations that eat up weeks of bench time.

    This compound, thanks to its unique set of substitutions, often lands in the sweet spot for accessing new molecular frameworks. Integrating it into multistep syntheses lets chemists bypass convoluted routes, going straight to key intermediates. In a world where project cycles now move faster than ever, tools like this produce measurable advantages, bridging early-stage ideas to finished candidates at record pace.

    Environmental Responsibility and Waste Disposal

    With heightened awareness around green chemistry, every decision on reagent use ripples through environmental accountability. Halogenated pyrimidines like this one warrant careful disposal to prevent soil or water contamination. Local rules dictate hazardous waste protocols, but in my group, we integrate waste minimization early into experimental design — combining reactions or recycling solvents where possible.

    Reduction in waste isn’t just about safe disposal; it often comes from planning reactions around versatile intermediates that deliver more value per synthesis. Using this compound’s pattern of reactivity, fewer steps and fewer auxiliary chemicals find their way to the waste barrel. Not every substitute can make that claim, and those benefits matter when reporting back to funding agencies or environmental review boards.

    The Learning Curve: Training and Knowledge Transfer

    Students and junior researchers quickly see the value in a reagent that works reliably across different classes of reactions and in various solvents. The structure of 3-Amino-5-Bromo-2-Fluoropyrimidine makes it easy to teach methods for Pd-catalyzed couplings, nucleophilic aromatic substitution, or heterocycle elaboration. I’ve seen early-career chemists gain confidence moving from bench to paper, connecting what they learn directly to project outcomes using this compound.

    Institutions with rotating staff or rapid turnover benefit from intermediates that behave predictably, shortening the ramp-up for new projects and spreading best practices without constant troubleshooting. The more complicated or specialized a reagent, the higher the learning curve creeps — losing precious innovation time to basic orientation. Reliable tools like this convert classroom concepts into real-world output quickly.

    Documenting Results and Supporting E-E-A-T Principles

    Reporting research grounded in reproducible, high-quality chemistry sits at the core of scientific progress. Good work with this compound translates effortlessly into detailed experimental methods, clear product characterization, and transparent data sharing. Experts who review manuscripts or patent filings look closely at supporting evidence for every reagent and yield claimed, with added scrutiny for less common heterocycles.

    Experience using 3-Amino-5-Bromo-2-Fluoropyrimidine builds both trust and authority when presenting results, expanding reputations for reliability. I’ve found that clear records — NMR spectra, MS traces, product verification — support grant applications and prove crucial during peer review or intellectual property examinations. Sharing both the chemical structure and practical notes on synthesis encourages others to replicate or extend the work, raising the standard for trustworthy, evidence-supported science.

    Looking Ahead: New Frontiers with Multifunctional Pyrimidines

    Advances in synthetic and medicinal chemistry often arrive through incremental innovation — not just discovering a new molecule but taking full advantage of flexible intermediates. 3-Amino-5-Bromo-2-Fluoropyrimidine, by virtue of its trio of functional groups, maps onto a wide variety of future projects, from tuning physicochemical properties to targeting new protein sites. The global research community stands to benefit from materials that offer dependable access to new ideas, saving precious cycles of trial and error.

    Each year, new leads appear in high-impact journals and patent filings, often tracing their roots back to simple, robust intermediates like this one. Whether driving efficiency, scientific rigor, environmental stewardship, or just plain curiosity, the impact of a well-chosen reagent ripples far beyond a single experiment. The next breakthrough may come from a well-organized lab shelf, with 3-Amino-5-Bromo-2-Fluoropyrimidine playing an unassuming, essential role in the process.