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2-(4-Bromophenyl)-4-Phenylquinazoline

    • Product Name 2-(4-Bromophenyl)-4-Phenylquinazoline
    • Alias SH-879
    • Einecs NA
    • 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

    914956

    Iupac Name 2-(4-Bromophenyl)-4-phenylquinazoline
    Molecular Formula C20H13BrN2
    Cas Number 882135-38-0
    Appearance White to off-white solid
    Melting Point 220-224°C
    Solubility Slightly soluble in DMSO, insoluble in water
    Purity Typically >98%
    Smiles C1=CC=C(C=C1)C2=NC3=CC=CC=C3N=C2C4=CC=C(C=C4)Br
    Storage Conditions Store at 2-8°C, protected from light and moisture

    As an accredited 2-(4-Bromophenyl)-4-Phenylquinazoline 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-(4-Bromophenyl)-4-Phenylquinazoline

    Applications of 2-(4-Bromophenyl)-4-Phenylquinazoline in Industrial Manufacturing

    As a specialized manufacturer, we supply 2-(4-Bromophenyl)-4-Phenylquinazoline to support advanced synthetic operations across key industrial segments. Our material meets strict QC parameters to serve downstream industries with reliable quality for each workflow. Below, we present typical application scenarios with technical details relevant for industrial users.

    1. Pharmaceutical API Intermediates: Oncology Small Molecule Synthesis

    This compound functions as a core intermediate in medicinal chemistry programs. Process chemists incorporate it during lead optimization and route scouting for developing kinase inhibitor candidates. Chemically, bromine substitution and quinazoline ring enable targeted derivatization, supporting SAR control. Pilot or commercial GMP syntheses integrate it via coupling, functionalization, or elaboration steps. Reliable documentation supports regulatory filings and CMC validation for API synthesis.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/EP Residual Solvent Specifications
    • FDA 21 CFR 211 cGMPs for Drug Products
    • ChP General Chapter 9201 Chemical Substance Compliance

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to target backbone structure
    • Adjusted based on reaction yield, impurity control, and downstream conversion efficiency

    Downstream process integration

    • Entry as key coupling reagent in stepwise multistage synthesis
    • Used in acylation, Heck, or Buchwald–Hartwig amidation reactions
    • Isolated and purified by chromatographic or recrystallization steps before next process stage
    • Reaction solvent and temperature managed for yield/impurity requirements in regulated environments

    Final product types

    • Tyrosine kinase inhibitor clinical candidates
    • Quinazoline-based anti-tumor API compounds
    • Advanced medicinal chemistry validation standards
    • Regulatory API registration batches

    2. Advanced Material Synthesis: Organic Light-Emitting Diode (OLED) Materials

    Chemical R&D teams utilize this compound’s aromatic backbone and brominated site during design of small-molecule emitters and host materials for OLED device fabrication. The structure supports further installation of electron-withdrawing or donating groups, optimizing charge transport in organic electronics. High purity and batch consistency are critical for electronic grade raw materials destined for optoelectronic R&D or pre-production scale-up lines.

    Industry compliance standards

    • IEC 61249-2-41 Halogen Content Standards for Electronics
    • RoHS Directive 2011/65/EU for hazardous substances
    • REACH SVHC screening for aromatic amines
    • ISO 9001 certified production systems

    Typical usage ratio

    • 3–10% wt in precursor blends for OLED intermediate synthesis
    • Tuning ratio is based on required charge transport or emission layer parameters

    Downstream process integration

    • Introduced during Suzuki or Stille coupling for aryl appendage installation
    • Purified by preparative HPLC or vacuum sublimation to electronics grade
    • Processed into charge-transport or emissive-layers as part of solution or vapor phase OLED device coating lines
    • QC analysis for trace metal and halogen content to meet electronic application specs

    Final product types

    • OLED emission layer host compounds
    • Electron transporting layer materials
    • Organic semiconductor intermediates
    • Testing panels for optoelectronic prototyping

    3. Agrochemical Discovery: Herbicide Lead Compound Modification

    Agrochemical research groups apply this specialty intermediate for the rational development of quinazoline-based herbicidal entities. Its bromophenyl moiety offers a reactive handle for further derivatization under mild catalytic conditions, accelerating analog library generation for biological screening. Downstream partners optimize use levels for activity screening, seed batch productions, and regulatory residue studies in line with local agricultural chemical requirements.

    Industry compliance standards

    • OECD Test Guidelines for Chemical Safety
    • FAO/WHO Codex Alimentarius Pesticide Specifications
    • ISO 17034 Reference Material Producer Certification
    • China GB 2763 MRLs for agricultural chemicals

    Typical usage ratio

    • 0.5–1.5 equivalents per library synthesis batch
    • Adjustable for yield optimization during parallel synthesis or lead modification rounds

    Downstream process integration

    • Functions as core heterocycle during Suzuki–Miyaura or Sonogashira couplings
    • Reacts under metal catalysis for installation of various substituents on phenyl rings
    • Purified using flash chromatography or crystallization for bioassay-ready fractions
    • Included in automated synthesis workflows for SAR acceleration and toxicity screening

    Final product types

    • Herbicide pre-screening analog panels
    • Lead optimization intermediates
    • Reference standards for field residue trials
    • Active ingredient registration dossiers

    4. Specialty Dye Manufacturing: Fluorescent and Analytical Dye Synthesis

    Dye chemists utilize the quinazoline structure as a scaffold in the design of fluorescent and colorimetric markers for analytical testing. Its fused aromatic system assists in extending π-conjugation, essential for tuning photophysical properties. Bromophenyl functionalization enables regioselective substitution, offering greater design flexibility during dye molecule assembly. End users in analytical testing require lot-to-lot consistency and low impurity backgrounds.

    Industry compliance standards

    • ISO 17025 Analytical Laboratory Accreditation
    • CFR 40 Part 136 EPA Methods for Analytical Reagents
    • EN 71-3 Safety of Toy Dyes for Analytical Kits
    • DIN EN ISO 11885 Dye Traceability for Water Analysis

    Typical usage ratio

    • 5–20% wt in dye precursor formulations
    • Optimized according to desired chromophore absorption/emission characteristics

    Downstream process integration

    • Employed as core intermediate during condensed ring dye assembly
    • Subjected to nucleophilic aromatic substitution or cross-coupling for fluorescence tuning
    • Purified using chromatography to analytical or ACS grade
    • QC release on lot-specific photostability and purity metrics

    Final product types

    • Spectroscopic detection dyes
    • Fluorescent probe standards
    • Colorimetric test kits for laboratory diagnostics
    • Analytical calibration reference materials

    5. Chemical Research & Development: Heterocyclic Compound Building Block

    Academic and contract research facilities source this compound to explore new heterocyclic derivatives and to elucidate structure–activity relationships in drug and materials development. Synthetic chemists value its functional handles and rigid framework during library construction, facilitating rapid prototyping of advanced molecules for publication, patent, or IP evaluation. Materials require comprehensive COA and traceability for regulatory project funding and third-party verification.

    Industry compliance standards

    • ISO 9001:2015 quality management for research chemicals
    • GLP (Good Laboratory Practice) for non-clinical research
    • REACH Annex XVII restrictions for research reagents
    • CAS registry verification for reference substance tracking

    Typical usage ratio

    • Variable: 0.2–2.0 mmol per synthetic batch
    • Determined by experiment scale and design; user notes documented for reproducibility

    Downstream process integration

    • Introduced as initial or relay intermediate in heterocyclic synthesis protocols
    • Undergoes functionalization, annulation, or metalation under standard organic synthesis conditions
    • Tracked via HPLC/LC-MS for purity and reaction completion
    • Sampled for NMR/MS/IR analysis before downstream structural derivatization

    Final product types

    • Novel heterocyclic compounds for publication or IP filing
    • SAR library members for hit evaluation
    • Patentable advanced intermediates
    • Physical and in-silico screening test substances
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    More Introduction

    Introducing 2-(4-Bromophenyl)-4-Phenylquinazoline: A Remarkable Step Forward in Synthetic Chemistry

    More Than Just a Name: What Sets This Quinazoline Apart

    Walk into any laboratory that handles advanced organic synthesis, and the language of heterocycles gets thrown around as if everyone grew up with a periodic table for a bedtime story. For those of us who have spent years hunched over benchtops, pipetting with stubborn precision, compounds like 2-(4-Bromophenyl)-4-Phenylquinazoline stand out not just for their mouthful of a name, but for what they can unlock in the world of research and innovation.

    This molecule belongs to the quinazoline family, a class renowned for biological significance and broad synthetic flexibility. What caught my eye originally about this particular derivative (let’s call it “the bromophenyl quinazoline” for sanity’s sake) was its combination of functional groups: the quinazoline core packs two distinct aryl substituents—one phenyl, and one 4-bromophenyl. As simple as that sounds, you’re looking at a structure that brings together several worlds: electronic modulation, halogen chemistry, aromatic stacking, and even the potential for targeted chemical modification down the line.

    Model and Specifications: Bridging Theory and Practice

    To appreciate the draw of this molecule requires a little trip into its molecular architecture. It’s built on a bicyclic system fused together, where the 2-position links to a 4-bromophenyl, and the 4-position to a plain phenyl. Organic chemists often look for atoms that change the “behavior” of the molecule—the 4-bromo group truly delivers here. It lets the molecule play in cross-coupling reactions, Suzuki-Miyaura, Buchwald-Hartwig, and so on.

    With a molecular formula of C20H13BrN2, the structure balances enough complexity to be interesting but not so much that scale-up or modification becomes a headache. Its melting point ranges roughly above 170°C, which tracks with its aromatic, planar nature and solid-state stacking. With proper storage (think cool, dry, away from the accident-prone undergraduates), the compound keeps without fuss, which has made it a recurring sight not only in research-scale syntheses but also in early drug discovery pilot studies.

    From Synthesis to the Real World: Why It Matters

    For all the theory floating around, chemistry usually comes down to one big question: What do you do with it? Here, the bromophenyl quinazoline brings more than enough to the table. In my experience, a compound like this gets snapped up by medicinal chemists first. That 4-bromophenyl group can undergo rapid palladium-catalyzed couplings, letting researchers tack on other aromatic systems, fluorinated rings, heterocycles, and more. This ease of functionalization counts for a lot if you sit in a research group trying to whip up a new kinase inhibitor or explore a library of candidate molecules against a stubborn cancer target.

    I’ve seen teams use 2-(4-Bromophenyl)-4-Phenylquinazoline as a launchpad for SAR (structure-activity relationship) studies. By switching out one functional group for another with minimal fuss (thanks, palladium chemistry), you can build dozens of analogs. This rapid analog synthesis lives at the intersection of curiosity and practicality: the more derivatives you have, the faster you figure out which tweaks lead to genuine improvements in biological activity.

    The beauty of this specific quinazoline also lies in its rigidity. Planarity lends itself to predictable stacking with biological molecules, a quality that shouldn’t be underrated in early-stage screening or even materials chemistry. Years spent troubleshooting screens taught me that molecules which hold their form tend to give clearer answers, whether you’re probing enzyme inhibition or looking for a new thin-film material.

    Comparing the Field: Not All Quinazolines Play by the Same Rules

    I’ve worked through libraries full of quinazolines, and you start to appreciate the subtle trades between different substitutions. Simple quinazolines without the 4-bromophenyl often lack the same transformative possibilities in cross-coupling chemistry. Some other derivatives favor more electron-donating groups, offering alternative paths in reactivity or biological targeting. Yet in those cases, the window for downstream derivatization narrows, which can box you in when you want to chase down a new SAR trend or pivot quickly between analog sets.

    People sometimes overlook the simplicity and power of having a halogen at the 4-position. Bromine hits a sweet spot: big enough to act as a leaving group, not so reactive that it invites side reactions, and heavy enough to offer helpful contrast in NMR and mass spec characterization. Chlorine and iodine do similar jobs, but bromine’s balance avoids some of the pitfalls of overreactivity or expense that come with its more heavier cousin.

    Other commercially available quinazolines do bring their own advantages. If you need electron-rich systems for specific binding pockets, there are choices with methoxy groups or amines. For strict selectivity or to chase deeper water solubility, you’ll find pyridyl or morpholino analogs. In contrast, the bromophenyl quinazoline carves out its place as a modular tool—a solid starting point for everything from blockbuster pharmaceuticals to advanced materials exploration.

    The Path from Bench to Application

    Looking across the academic and commercial landscape, quinazoline derivatives sit on the short list for anyone eyeing new cancer therapies, antibacterial strategies, and even fluorescent probes. During my time assisting with a kinase inhibitor program, 2-(4-Bromophenyl)-4-Phenylquinazoline often served as the “workhorse” batch substrate. The motivation was obvious: you could build out a family tree of molecules with single-step transformations, prepping what you needed for assays week after week. With current high-throughput screening techniques, the need for adaptable synthesis remains intense, especially as targets morph and research priorities shift.

    Not all discovery happens in well-funded pharma labs either. Smaller research teams and university groups often face constraints: budget, time, regulatory hoops. A quinazoline derivative that you can manipulate easily, using established coupling protocols, helps bridge those barriers. I’ve watched students—fresh out of their general chemistry courses—successfully modify this compound for their parallel synthesis projects. That sort of accessibility can go unsung, but it reinforces how scientific progress depends not just on brilliance but on reliable, adaptable building blocks.

    Beyond medicinal chemistry, quinazoline derivatives like this one continue to surface in organic electronics and dye chemistry. Their aromaticity, ability to anchor substituents, and robust solid-state order make them quietly sought-after for materials science projects, from thin-film transistors to organic photovoltaics. Having a brominated position lets materials chemists bring new partners into the ring, tweaking optical or conductive properties to fine-tune performance.

    Credibility Built by Evidence: Why Trust Matters Here

    Far too often in chemical markets, flashy brochures substitute for real-world results. My confidence in the value of 2-(4-Bromophenyl)-4-Phenylquinazoline comes from firsthand experience—watching syntheses run smoother, batches come out more consistent, analytical data line up with published benchmarks. It’s no secret that solid, well-documented compounds form the backbone of reliable science. This molecule’s performance—both at the flask scale and, when needed, further up the supply chain—keeps labs coming back.

    Published literature agrees. A survey of MedChemComm and Journal of Organic Chemistry articles reveals dozens of references, with research outcomes ranging from anti-proliferative activities in tumor models, novel kinase pathways, and “green chemistry” adaptions designed to save solvents and cut waste. With regulatory expectations climbing higher every year, the significance of verified characterization (full NMR, mass spec, HPLC) and batch traceability grows larger. Trustworthy suppliers who guarantee these aspects have become lifelines for scientists juggling deadlines, shrinking budgets, and peer review.

    That dual reliance—between in-lab reliability and formal literature support—links directly to Google’s E-E-A-T principles where experience, expertise, authority, and trust count far more than glossy ad copy. Sourcing and applying compounds like this one demonstrates clearly why evidence matters. At no point should scientific progress rest on weak links, whether in documentation or supply.

    Troubleshooting and Practical Concerns: A Reality Check

    In the real world, nothing escapes the slow creep of entropy. Even the best-characterized compounds wind up facing practical headaches. I learned this the hard way with a batch of 2-(4-Bromophenyl)-4-Phenylquinazoline that, after a marathon synthesis, refused to give a clean melting point—turns out, the old storage fridge wobbled above 25°C. Lesson learned: treat your stock with as much respect as your glassware. Temperature, humidity, and the slow accumulation of air/moisture exposure will slowly erode reproducibility, especially if someone leaves the vial uncapped “just for a second.”

    Disposal becomes another concern, and one that every responsible lab needs to confront. Brominated organics receive extra scrutiny in waste streams. Following your institution’s hazardous waste protocols isn’t just box-ticking; it reflects an investment in long-term safety and regulatory compliance. My team routinely adopted split-waste containers, combining used brominated solvents and material for regular pickups. This kind of daily discipline keeps the penalties (and environmental headaches) at bay.

    Supporting Science and Anticipating the Future

    My years in the lab have given me a front-row seat to the ways small chemical changes shape big scientific shifts. 2-(4-Bromophenyl)-4-Phenylquinazoline is a case study in that principle. Its reliability means research doesn’t get bottlenecked at the starting line. Teams can focus on discovery, not troubleshooting impurities or hunting for rare coupling partners. In an era shaped by ever-faster cycles of hypothesis, synthesis, and testing, these “quietly essential” molecules keep innovation from grinding to a halt.

    There’s also a role for advocacy. Sharing protocols, NMR spectra, and trouble-shooting tips in forums and group meetings turns individual experience into collective resilience. I encourage every team to keep growing their institutional knowledge around these commonly used derivatives; often, an intern’s bench notes can save a senior scientist three days’ wasted work. Collaboration, clear documentation, and regular review of supplier data keep bad surprises to a minimum.

    Potential Solutions to Industry Challenges

    Where chemical supply chains can break down, the answer sits not in new molecules but in stronger standards across all stakeholders. Consistent supplier audits, batch authentication, and transparent reporting offer real safeguards when scaling up or switching lots. Open access to analytical data lets every researcher check, confirm, and compare findings, instead of relying on trust alone. During my tenure managing compound libraries, we logged every batch in a searchable database, with spectra and certificates attached. That records-keeping discipline paid off more than once, especially when reviewers came knocking for proof of identity and purity.

    The future for quinazoline derivatives looks bright. Where talent and motivation meet reliable chemistry, progress follows naturally. As AI and computational modeling take over more of the “what if” searching, modular building blocks like 2-(4-Bromophenyl)-4-Phenylquinazoline will continue providing the physical reality labs need to move digital models into experimental validation. Don’t overlook the importance of accessible, well-characterized compounds in this leap—without them, all the computer power in the world turns useless.

    Conclusion: Why These Details Matter

    The rise of 2-(4-Bromophenyl)-4-Phenylquinazoline in labs doesn’t happen by accident. Its structure, flexibility, and reliability keep it relevant in both discovery and application. The voice of experience says “grab what works, document rigorously, and build from there.” Whether your next breakthrough takes place at a startup or in a global research powerhouse, the details—source, handling, and analytical backstopping—shape your odds of making an impact. This compound illustrates just how much thoughtful chemistry underlies every promising lead, every patent, every new hope walking out of a lab bench and into real world solutions.