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2-Bromo-4,6-Diphenylpyrimidine

    • Product Name 2-Bromo-4,6-Diphenylpyrimidine
    • Alias 2-Bromo-4,6-diphenylpyrimidine
    • Einecs 697-809-6
    • 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

    210011

    Chemicalname 2-Bromo-4,6-Diphenylpyrimidine
    Molecularformula C16H11BrN2
    Molecularweight 311.18 g/mol
    Casnumber 852180-43-1
    Appearance White to off-white powder
    Meltingpoint 139-141°C
    Solubility Slightly soluble in organic solvents (e.g. DMSO, DMF)
    Purity Typically >98%
    Storageconditions Store at 2-8°C, protected from light and moisture
    Smiles C1=CC=C(C=C1)C2=NC(=NC(=C2)Br)C3=CC=CC=C3
    Inchi InChI=1S/C16H11BrN2/c17-16-18-14(10-6-2-1-3-7-10)12-15(19-16)11-8-4-5-9-13(11)12/h1-9,12H

    As an accredited 2-Bromo-4,6-Diphenylpyrimidine 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-4,6-Diphenylpyrimidine

    Applications of 2-Bromo-4,6-Diphenylpyrimidine in Industrial Manufacturing

    As the direct manufacturer of 2-Bromo-4,6-Diphenylpyrimidine, we focus on the material’s key industrial applications across advanced chemical synthesis fields. Each application below details its unique regulatory frameworks, usage parameters in formulation, downstream process integration, and end-use product categories supplied by our global clients.

    1. Pharmaceutical Intermediate in Kinase Inhibitor Synthesis

    2-Bromo-4,6-Diphenylpyrimidine finds substantial demand as a reactant in the targeted synthesis of novel kinase inhibitors. Medicinal chemistry teams utilize this compound for constructing core pyrimidine scaffolds present in multiple oncology and inflammation therapeutics. During the API (Active Pharmaceutical Ingredient) development phase, scientists employ it in Suzuki or Buchwald couplings to elaborate specific functional groups required for receptor binding and pharmacokinetics. Its use aligns with multi-step synthesis routes, subjected to rigorous analytical monitoring and controlled under validated process conditions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (cGMP for Finished Pharmaceuticals, US FDA)
    • European Pharmacopoeia monograph reference as applicable
    • USP <797> for compounding controls (where intermediates handled on site)

    Typical usage ratio

    • Usage ranges from 0.5 to 1.2 mol per mol of final pyrimidine core, adjusted by step yield, desired substitution pattern, and impurity profile.

    Downstream process integration

    • Charged during the early or mid-stage construction of heterocyclic building blocks, specifically prior to final scaffold elaboration and downstream functionalization. Integrated into continuous or batch flow reactor systems.

    Final product types

    • Small molecule kinase inhibitor APIs
    • Branded and generic anti-cancer drug substances
    • Investigational oncology compounds for clinical development
    • Reference standards for pharmaceutical research

    2. Intermediate for Agrochemical Synthesis (Herbicides & Fungicides)

    Chemical synthesis groups in the agrochemical industry use this compound as a pyrimidine core builder for advanced fungicidal or herbicidal agents. It enables stepwise functionalization, leading to selective pesticides addressing resistant weed and fungal strains. Quality teams oversee analytical release, while process chemists apply it in scale-up reactions alongside optimized catalyst systems and solvent controls. The compound ensures robust molecular backbone development prior to final formulation and regulatory testing.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • ISO 9001 Quality Management System
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products)
    • REACH Registration (European Chemicals Agency)

    Typical usage ratio

    • 0.7–1.0 mol per mol of final active ingredient precursor; adjusted based on active loading levels and side chain modifications.

    Downstream process integration

    • Introduced during intermediate stages of active agrochemical ingredient construction, supporting further halogenation, alkylation, or coupling steps prior to crystallization and downstream formulation.

    Final product types

    • Triazole-based fungicides
    • Diphenylpyrimidine herbicides
    • Pyrimidine-heterocycle pesticide actives
    • Custom agricultural synergists

    3. Material for OLED and Organic Electronics Synthesis

    R&D and scale-up units in electronics materials incorporate this pyrimidine derivative as a key starting material or functionalization agent in small molecule OLED (Organic Light Emitting Diodes) and OFET (Organic Field Effect Transistor) architecture. Used in complex coupling and crosslinking reactions, it contributes to the charge transport layer or emissive domains, impacting device stability and performance. Process engineers monitor impurity profiles and solvent selection during pilot and commercial stages under stringent purity protocols.

    Industry compliance standards

    • IEC 62321 (Determination of certain substances in electrotechnical products)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 14001 Environmental Management System
    • JEDEC JESD625B Handling, Packaging, Shipping & Use of Moisture/Reflow Sensitive Devices

    Typical usage ratio

    • Emission layer synthesis: typically 0.4–1.5 mol per mol of small molecule host or guest structure, tuned by emissive property targets.

    Downstream process integration

    • Utilized as a coupling partner in key palladium-catalyzed reactions, forming the electron transport layer precursor or luminescent framework applied during advanced OLED fabrication and device coating steps.

    Final product types

    • Small molecule OLED emitters
    • Organic thin-film transistor precursors
    • Printable optoelectronic inks
    • Electronic grade materials for display manufacturing

    4. Intermediate for Specialty Dye and Pigment Manufacture

    Manufacturers of high-performance specialty colorants employ this compound in the synthesis of advanced heterocyclic dyes and pigments. The aromatic pyrimidine structure lends itself to tailored chromophore engineering, enhancing UV stability, fastness, and color characteristics in polymer, textile, and ink formulations. Batch production requires precision in reaction temperature and purification stages, as well as compliance with downstream regulatory screening for end-use sectors.

    Industry compliance standards

    • EN 71-3:2019 (Migration of certain elements in toy pigments/inks)
    • REACH Annex XVII for pigment safety in textile and plastic applications
    • ISO 787 General Methods of Testing Pigments and Extenders
    • ZDHC MRSL for restricted chemical substances in fashion industry dyes

    Typical usage ratio

    • 0.8–1.4 equivalents per mol of final chromophore; actual dosage optimized based on pigment tone and molecular structure customization.

    Downstream process integration

    • Incorporated into dye synthesis at the chromophore-building step, especially for biphenyl and pyrimidine core modifications before further derivatization and finishing stages such as milling and granulation.

    Final product types

    • High-performance organic pigments
    • Special effect dyes for plastics and coatings
    • Textile fiber colorants with advanced lightfastness
    • Electronic display inks with controlled charge mobility

    5. Building Block for Liquid Crystal Material Development

    Developers of liquid crystalline compounds in advanced display technologies utilize this material for synthesizing diphenylpyrimidine-based rod-shaped molecules. The rigid aromatic structure, combined with its functional bromide group, allows precise introduction into mesogenic cores. QC and process groups set tight release specifications to ensure purity, crucial for dielectric anisotropy and viscosity requirements in liquid crystal display formulations. Production teams handle the synthesis under inert conditions, monitoring residual bromine and byproduct control for downstream integration.

    Industry compliance standards

    • IEC 61249-2-21 for halogen-free laminated material assessment
    • RoHS 3 (EU 2015/863) for display electronic substances
    • ISO 9001:2015 for materials management
    • Customer liquid crystal purity and residual halide specification (custom QC agreement)

    Typical usage ratio

    • 0.9–1.1 mol per mol of mesogenic compound synthesized, adjusted for substitution pattern and molecular length requirements.

    Downstream process integration

    • Feeds into the primary coupling reaction during mesogen core assembly, influencing phase transition properties and later purification stages prior to blending and cell filling.

    Final product types

    • Liquid crystal display (LCD) mixture components
    • Specialty nematic and smectic phase materials
    • Advanced display panel fillers
    • Prototyping chemicals for flexible screen R&D
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    More Introduction

    Discovering the Value of 2-Bromo-4,6-Diphenylpyrimidine in Modern Chemistry

    Stepping Into the World of 2-Bromo-4,6-Diphenylpyrimidine

    Curiosity about new chemical compounds never really fades if you’re in a lab that deals with heterocycles and fine chemicals. I’ve found that the molecules with a pyrimidine core always seem to find their way into the toolkit of medicinal chemists and research scientists. The one on the table today, 2-Bromo-4,6-Diphenylpyrimidine, doesn’t look flashy at first glance, but anyone who’s handled it can spot its value. Its structure combines a bromine atom at the 2-position and phenyl groups at the 4 and 6 positions substituting the classic pyrimidine ring, which unlocks some unique chemistry you just can’t always achieve with pyrimidine analogues.

    Turning Structural Features Into Real-World Applications

    The first thing you notice with 2-Bromo-4,6-Diphenylpyrimidine is its solid physical form. In my experience, it’s easy to store and typically comes as an off-white powder, making it straightforward to weigh and handle. Its chemical formula—C16H11BrN2—doesn’t make it leap out from a list, but the presence of both aromatic groups and the bromine atom sets it up to be far more than just another pyrimidine derivative. The real specialty comes from the combination of the electron-withdrawing bromo group and the bulky phenyl rings, which together help drive specific reactions in organic synthesis.

    Chemists looking to build new pharmaceuticals find the substitution pattern of this molecule useful. The bromo group offers a point of reactivity for classic coupling reactions, especially Suzuki or Buchwald-Hartwig cross-couplings. Personally, I have used it when there’s a need to introduce diverse aromatic groups at the 2-position for structure-activity relationship studies; those phenyl rings tend to increase lipophilicity and change how the compound interacts with biological targets. There’s a reason research groups keep ordering it for both library syntheses and as a strategic intermediate during route scouting.

    Why Choose a Bromo-Substituted Pyrimidine Like This One?

    Choosing 2-Bromo-4,6-Diphenylpyrimidine compared to other halogenated or non-halogenated pyrimidines comes down to control and versatility. The bromine at the 2-position is more reactive than its chloro or fluoro cousins but less of a handful than the iodo version, which I’ve seen decompose in solution if you’re not careful. With the phenyl groups flanking the ring, you get a degree of steric hindrance, which can help selectivity in reactions. When running a Suzuki cross-coupling, this middle ground reactivity often leads to cleaner product profiles, something that only those of us who’ve watched a TLC plate develop for over an hour trying to chase impurities really understand.

    Other similar pyrimidines might come cheaper or in larger bulk, but the fine balance of reactivity and stability found here cannot always be matched. Years in the lab taught me that swapping out a bromo for a chloro version—hoping to get some cost savings—tends to produce worse yields, longer reaction times, and far more column chromatography work. More than one frustrated comment in my notebook attests to that lesson.

    Specifications That Matter in the Lab

    From a practical perspective, the melting point of 2-Bromo-4,6-Diphenylpyrimidine hugs the mid-200s°C range, giving confidence about its thermal stability in most reaction conditions you’d consider for cross-coupling or nucleophilic substitution. Its solubility isn’t spectacular in pure water, but shows good compatibility with a range of organic solvents such as dichloromethane, DMF, and toluene, all fairly common choices among synthetic chemists. I learned quickly to pull out a fresh bottle of anhydrous solvent when working with it; trace water often slows reactions considerably.

    The biggest upside comes from the purity that’s reliably achievable through standard silica gel chromatography. Most suppliers, and the batches I’ve tested, hit well above 98% purity on HPLC. That brings a bit of relief when deadline pressures or tight project milestones roll around. Comparing this comfort with working on less refined starting material is a night-and-day difference: more consistent yields, predictable behavior in scale-up, fewer by-products.

    Digging Deeper—How Do Scientists Use It?

    You likely spot this compound frequently in medicinal chemistry groups chasing kinase inhibitors and other targets requiring pyrimidine scaffolds. Those twin phenyl groups can hold together intramolecular stacks, stabilize three-dimensional structures, and provide handles for later functional group modifications. I’ve seen academic groups and pharmaceutical giants alike explore its power in developing new heterocyclic libraries, hitting targets where smaller or less aromatic pyrimidines just don’t do the job. It’s not just a matter of swapping in a new functional group; the synergy between the bromo and the phenyl rings means you’re essentially offering a new shape and electronics to the enzyme or receptor.

    Some of my peers have turned to this compound when developing fluorescent probes or advanced materials, allowing the rigid core and reactive bromo site to serve as attachment points for dyes or other reporter units. The synthetic accessibility of derivatives, starting from this core, facilitates the creation of molecules for imaging or optoelectronic applications. This versatility means it enters as an intermediate but can easily end up in the final target molecule, especially for highly specific applications in science and engineering.

    Standing Apart—The Difference from Other Pyrimidine Products

    Not every pyrimidine derivative can stand up to multi-step synthesis or the real-life demands of pharmaceutical research. I’ve seen too many analogues fall flat—poor stability, limited compatibility with metal catalysis, frustrating precipitation out of solution, and inconsistent performance across batches. The 2-bromo substitution provides that essential kick in reactivity for cross-coupling, while the phenyls prevent excessive polymerization or tar formation during scale-up. This balance saves countless hours otherwise wasted in troubleshooting and purification.

    There’s also another side, often overlooked in theoretical discussions. In hands-on research, ease of purification becomes a kind of lifeline. Chromatography columns load up quickly with 2-Bromo-4,6-Diphenylpyrimidine thanks to its robust aromatic character, eluting cleanly and minimizing waste. Compare that to some non-brominated precursors—you need to run extra steps to coax the product out of the muck. One of the rare luxuries in a busy synthesis lab is saving time while gaining more reliable quality with compounds like this one.

    Looking at the whole picture, I’ve weighed and run reactions with a range of related pyrimidines, and the challenges that crop up with less sophisticated alternatives never hit as hard with the phenyl-bromo motif. Reactions proceed cleaner; yields remain competitive; purification is a breeze. These differences translate into lower risk for failed syntheses, which is what matters most in the long run—especially with resource-strapped projects or in smaller research outfits where efficiency is non-negotiable.

    Key Considerations for Chemists Selecting This Compound

    Choosing a new reagent can stir up anxiety, especially first time a group invests in a bulk purchase. Reliability, stability, and proven track records mean more than marketing claims. From what I’ve seen, 2-Bromo-4,6-Diphenylpyrimidine maintains shelf stability well, even over extended storage, as long as the bottles are kept dry and away from light. Moisture sensitivity seems low, based on repeated open-and-close cycles in our own inventory, though best practices always guide you to use gloves and keep containers sealed.

    Handling is straightforward, with no unusual hazards beyond those expected of a standard bromoarene. Material Safety Data Sheets consistently peg it as a moderate irritant. In keeping with good research habits, I always recommend standard fume hood procedures and minimizing direct contact. There’s a certain peace of mind when a compound comes with clear, consistent safety guidance and manageable hazards—unlike the unpredictable nature of some alternatives, especially those in earlier stages of commercial availability.

    Impact on Research and Industry

    Since entering wider circulation, 2-Bromo-4,6-Diphenylpyrimidine has carved out a niche in both academic and industry settings. High-throughput screening groups enjoy its compatibility with automated platforms, which require batch-to-batch consistency and minimal background reactivity. Scale-up chemists in pilot plants praise its robustness and tolerance to temperature variation, which reduces risk in larger reactors. I appreciate how the predictable handling profile lowers the risk threshold, allowing more aggressive experimentation earlier in the development timeline.

    There’s real pride in watching a compound become a “go-to” building block, not just a specialty item for a narrow application. Colleagues at both university and contract research settings have echoed this sentiment—one recounted a program that only hit its success milestones after switching to bromo-phenyl pyrimidine intermediates for late-stage diversification. The savings in time, cost, and labor ripple through all aspects of the synthesis campaign.

    Pushing the Boundaries: How 2-Bromo-4,6-Diphenylpyrimidine Enables New Discoveries

    Beyond pharmaceuticals, novel heterocyclic structures, and screening libraries, this compound shows promise in building advanced molecular scaffolds for sensors, dyes, and functional materials. Its molecular rigidity and tailored reactivity have led it into the sights of researchers working in areas I never expected when I first encountered it. Supramolecular chemists, interested in π–π stacking and electronic donor-acceptor frameworks, leverage the phenyl subsitutents for assembling new materials. The easily replaceable bromo site is often exploited in the design of ligands for catalysis, solid-supported materials for separations, and as cross-linking nodes in organic electronics.

    In my own work, alternative starting materials never provided the same synthetic leverage. More fiddling with reaction conditions, unexpected side products, or poor reproducibility surfaced with less elaborate pyrimidines. New reactivity sometimes emerges with 2-Bromo-4,6-Diphenylpyrimidine, opening doors for making molecules that simply weren’t feasible with more basic precursors.

    Solutions for Common Synthetic Challenges

    I know the hunt for efficiency never stops in chemical research. So many times, project progress gets derailed by bottlenecks in key coupling steps or hard-to-purify side products. Having a stable, reactive aryl bromide that doubles as a rigid building block helps hit project timelines and research goals. For teams chasing unknowns—either by exploring SAR series or screening hundreds of derivatives—starting from 2-Bromo-4,6-Diphenylpyrimidine trims down complexity and raises the rate of success.

    I often remind new chemists: efficiency means using the best tool, not always the cheapest. Saving hours in purification or improving yields pays real dividends in both academic and industrial research. In my experience, this compound speeds up optimization, letting teams move from hit to lead with much less trial-and-error. Less troubleshooting means more time spent on creative exploration—the real value of reliable intermediate chemistry.

    Expertise and Trust Built Over Time

    Having spent years tracking down reliable building blocks, I value compounds that stay consistent and resist batch variability. I’ve learned to favor intermediates supported by robust data, established usage, and trusted publication histories. 2-Bromo-4,6-Diphenylpyrimidine qualifies, supported by a healthy stream of peer-reviewed publications, cited patents, and open-access studies. Evidence from the public literature documents syntheses, cross-couplings, and biological evaluations, reinforcing its reputation.

    To build trust, I look for analytical data from real-world use, not just supplier certificates. Independent validations by researchers strengthen confidence in its performance. I’ve also watched positive case studies emerge from both global corporations and upstart contract research organizations—each applying the compound to different domains and reporting favorable outcomes.

    The best endorsements don’t come from advertisements. They come from scientists like myself, passing tips down through lab meetings, conference chatter, and technical reports. The evolution of 2-Bromo-4,6-Diphenylpyrimidine from a novelty to a mainstay illustrates how tools chosen with care can unlock better results, faster progress, and more meaningful discoveries.

    Looking Ahead—Expanding Horizons

    With the explosion of interest in new modalities, such as targeted protein degradation, fragment-based drug discovery, and next-generation optoelectronics, compounds like 2-Bromo-4,6-Diphenylpyrimidine gain even more importance. The demand for robust, versatile, and high-performance intermediates rises each year. I see more groups exploring its use beyond classic pharmaceuticals—pushing into chemical biology, green chemistry, and smart materials.

    Younger chemists entering the field appreciate how it simplifies workflows and lowers barriers to entry. With so many new entrants and cross-disciplinary programs, having reliable building blocks levels the playing field. Years from now, I expect 2-Bromo-4,6-Diphenylpyrimidine’s role will continue to grow, branching into unexpected new technologies as emerging industries look for ways to combine classic chemical performance with new forms of innovation.

    Final Word: Why Personal Experience Matters When Choosing Chemical Tools

    Experience has taught me to value solutions that solve real problems, not just those that look good on paper. 2-Bromo-4,6-Diphenylpyrimidine isn’t just another catalog item; it’s a molecule with proven merits, practical advantages, and broad opportunities for those willing to test its limits. Differences between products often manifest at the bench—where it counts—making hands-on experience as important as any synthesis protocol or technical data sheet. That’s where compounds like this truly prove their worth, helping researchers move faster, cleaner, and more effectively towards answers that matter.