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7-Bromo-2,3-Dihydro-Isoindol-1-One

    • Product Name 7-Bromo-2,3-Dihydro-Isoindol-1-One
    • Alias 7-Bromo-isoindolin-1-one
    • Einecs 629-725-4
    • 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

    907261

    Product Name 7-Bromo-2,3-Dihydro-Isoindol-1-One
    Molecular Formula C8H6BrNO
    Molecular Weight 212.04 g/mol
    Cas Number 80211-72-7
    Appearance Off-white to pale yellow crystalline solid
    Melting Point 95-99°C
    Purity ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles O=C1CN(C2=CC=CC(Br)=C2)C1
    Inchi Key CPZKBXFELNTLMS-UHFFFAOYSA-N
    Storage Conditions Store in a cool, dry place
    Synonyms 7-Bromo-phthalimidine
    Hazard Statements May cause irritation to skin, eyes, and respiratory tract

    As an accredited 7-Bromo-2,3-Dihydro-Isoindol-1-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 7-Bromo-2,3-Dihydro-Isoindol-1-One

    Applications of 7-Bromo-2,3-Dihydro-Isoindol-1-One in Industrial Manufacturing

    As a dedicated producer of 7-Bromo-2,3-Dihydro-Isoindol-1-One, we supply this specialty intermediate to leading downstream manufacturers in pharmaceutical, agrochemical, pigment, and advanced materials industries. Below we outline precise application scenarios where our product delivers functional benefits, outlining regulatory, formulation, process, and end-use specifics for each sector.

    1. Pharmaceutical API Intermediate Synthesis

    In pharmaceutical process development, 7-Bromo-2,3-Dihydro-Isoindol-1-One is frequently integrated as a core building block for isoindolinone-containing small-molecule APIs, especially psychoactive drugs and selective CNS agents. Our manufacturing process delivers batch-to-batch consistency that supports multistep route validation and late-stage clinical development. This intermediate participates in Suzuki–Miyaura or Buchwald–Hartwig couplings, serving as a precursor for high-purity active pharmaceutical ingredients under strict ICH Q7 guidelines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for APIs
    • USP <795> and <797> for handling of pharmaceutical compounding intermediates
    • EU GMP Annex 1 for active substance production
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • Used at 0.5–1.2 molar equivalents relative to primary coupling partners, depending on target molecule structure and purity yield targets in the synthesis route

    Downstream process integration

    • Dissolved in anhydrous polar aprotic solvents as a halogenated aryl-amine precursor for Pd-catalyzed cross-coupling reactions in multistep pharmaceutical synthesis; followed by purification through column chromatography or crystallization

    Final product types

    • Neuroprotective drug candidates
    • Selective serotonin receptor ligands
    • Patent-protected CNS active pharmaceutical ingredients
    • Generic isoindolinone-derivative pharmaceuticals

    2. Agrochemical Active Compound Synthesis

    Manufacturers in the crop protection sector employ 7-Bromo-2,3-Dihydro-Isoindol-1-One as a functionalized aromatic precursor for processing advanced herbicide and fungicide actives based on isoindolinone backbones. Our product meets rigorous agrochemical synthesis requirements, integrating efficiently into commercial-scale reactions that produce safe, stable, and effective plant protection agents.

    Industry compliance standards

    • FAO/WHO specification for pesticide active ingredients (Specification Series)
    • ISO 17025 laboratory and batch QC/QA for agrochemical manufacturing
    • EU REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) compliance
    • Good Laboratory Practice (GLP) OECD guidelines

    Typical usage ratio

    • 0.8–1.4 molar equivalents in active compound synthesis, adjusted based on laboratory analytics for yield and side-product minimization

    Downstream process integration

    • Feeds into aromatic substitution and heterocycle construction steps; used as a core substrate during condensation and bromination reactions integrated into continuous batch agrochemical active formation

    Final product types

    • Systemic seed-treatment fungicides
    • Selective pre-emergence herbicides
    • Crop growth regulatory agents containing the isoindolinone scaffold
    • Registered pesticide technical concentrates

    3. High-Performance Pigment Intermediate

    Downstream pigment formulators use our material for synthesizing brominated isoindolinone intermediates which impart enhanced thermal and light stability to specialty colorants. The compound enables strong chromophore development when condensed with specific aryl partners, resulting in pigments tailored for plastics, automotive, and high-durability coatings.

    Industry compliance standards

    • EN 71-3 Safety of Toys (Migration of certain elements in pigments for children’s products)
    • ISO 9001 for pigment manufacturing traceability and QC
    • REACH Annex XVII (Restriction of hazardous substances in pigments)

    Typical usage ratio

    • 5–12% by weight relative to total pigment batch, ranged based on target color intensity and application end-use (plastics, paint, ink)

    Downstream process integration

    • Incorporated directly in the bromination and condensation step during the synthesis of organic pigment intermediates; followed by coupling with chromogenic agents and filtered/dried during post-synthesis

    Final product types

    • Automotive coating pigments
    • High-strength plastic color masterbatches
    • Industrial printing inks
    • Performance pigment dispersions

    4. Advanced Materials: Organic Electronics

    Producers of organic electronic components value 7-Bromo-2,3-Dihydro-Isoindol-1-One for constructing heterocyclic rings in polyaromatic frameworks, critical for organic semiconductors and optoelectronic layer precursors. The product’s controlled halogenation enables precise tuning of electron affinity, supporting the formation of high-mobility polymers and charge-transport materials for cutting-edge device manufacturing.

    Industry compliance standards

    • IEC 62607-4-1 for organic electronic materials characterization
    • ISO 14001 for environmental control in electronic chemical manufacturing
    • RoHS Directive for restriction of hazardous substances in electronic materials

    Typical usage ratio

    • 1–3 mol% relative to total monomer feed in polymer synthesis; adjusted according to device performance testing and electronic property targets

    Downstream process integration

    • Engaged in Stille or Suzuki-type polycondensation as a functionalized monomer; enters the polymer backbone during resination, followed by solvent stripping and thin-film formation processes

    Final product types

    • Organic field-effect transistors (OFETs)
    • Light-emitting diodes (OLEDs)
    • Chemical sensors (field-deployed chip technology)
    • Flexible printed electronics
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    More Introduction

    7-Bromo-2,3-Dihydro-Isoindol-1-One: Science in Action

    Digging Into a Key Organic Compound

    Some discoveries in chemistry change the entire landscape—some work quietly in labs and factories but make a big difference just the same. The compound 7-Bromo-2,3-Dihydro-Isoindol-1-One fits into that latter category. Building blocks in organic synthesis attract careful attention, and this one deserves a closer look.

    The core structure, 7-Bromo-2,3-Dihydro-Isoindol-1-One, sits at the crossroads of science and practical application. Chemists appreciate its distinct structure: a dihydroisoindolinone backbone, decorated with a bromine atom on the seven spot. That kind of substitution pattern opens up all kinds of routes for chemical modifications, especially in fields working with pharmaceuticals, pigments, and advanced materials. A lot of innovation in medicine starts out with someone examining a molecule like this one, picturing its next transformation.

    Specifications That Matter

    It pays to get specific about quality. The pure white or off-white powder doesn’t just look clean — it comes with high chemical purity, often surpassing 98%. Trace impurities get measured in modern labs using robust analytical tools, including proton and carbon NMR, high-resolution mass spectrometry, and chromatography. Call it the chemistry world’s way of double-checking every claim. Moisture content stays low, and melting point ranges tightly. Details like these tell me something about how rigorous suppliers approach consistency. Every batch of 7-Bromo-2,3-Dihydro-Isoindol-1-One brings those standards and test results along for the ride — and relying on these numbers means fewer surprises down the line.

    All that accuracy adds up, especially once you start synthesizing complex compounds. If you’ve worked in a chemistry lab, you know the agony of tracing a reaction failure to a minor impurity in a starting material. One vendor’s “technical grade” might look only slightly off from purer grades, but tiny differences in bromine placement or leftover solvents can make or break your project. In my experience, going for reliable, high-quality sources of this compound always paid off, even if the price ran a bit higher per gram.

    Uses in Research — and Real Life

    The most meaningful value comes from what we can do with a compound. 7-Bromo-2,3-Dihydro-Isoindol-1-One plays well in the world of pharmaceuticals, where scientists use it as a key intermediate to build drug candidates. The bromine gives options: it’s a reactive handle for further functionalization. So chemists use it to create new bonds and swap in other chemical groups. These acts of molecular “Lego-building” sound abstract, but they’re the nuts and bolts behind new painkillers, antivirals, and sometimes drugs for rare diseases.

    Beyond the pharma world, this building block turns up in specialty dye chemistry and material science as well. The electron-rich core and that reactive bromine site allow for a wide palette of coupling reactions. I’ve seen it appear in the synthesis of advanced polymers and optoelectronic materials — the kinds of things that end up in semiconductors, solar panels, or even flexible electronics.

    So many research teams want compounds that allow greater control and creativity, and having a structure like this in the toolbox speeds things up. Give a synthetic chemist 7-Bromo-2,3-Dihydro-Isoindol-1-One, and you usually get back novel molecules that weren’t there on Monday.

    Stacking Up Against Other Isoindolinones

    Chemistry loves its small differences — change a single atom, and the outcome may shift entirely. Compared to isoindolinones without the bromine at position 7, this compound brings a higher degree of reactivity. That bromine serves as a launchpad for Suzuki couplings, Buchwald-Hartwig aminations, and other modern cross-coupling and substitution reactions. Synthetically, that means routes open up that just don’t exist with non-brominated analogs.

    Other derivatives may feature different halogen atoms — chlorine or iodine, for example. Each brings its own mix of reactivity and downstream potential. In my lab days, using the bromo-derivative often delivered the right mix of reactivity and manageability. Iodinated versions tended to react even faster but sometimes decomposed easier and brought more safety headaches. Chlorinated variants might feel too inert at times. So, 7-Bromo-2,3-Dihydro-Isoindol-1-One tends to sit in the practical sweet spot: active enough to enable transformations but not so wild that reactions get out of control.

    This compound also outperforms simple isatins or phthalimides if your work demands a secondary amide and a functioning ring system that tolerates further customization. It’s not just about lab tricks; this difference shows up when you scale from milligram runs up to pilot plant or multi-kilogram output. Things that work in a tiny flask can fall apart under real-world manufacturing, so robustness counts.

    The Human Side: Why This Compound Matters

    All these technical details mean something because they enable the discovery and industrial development that touch everyday lives. New medication pathways rely on accessible intermediates. The ability to introduce different groups on the molecule changes the pharmacokinetics and pharmacodynamics of prospective drugs. In real-world language, this means better treatments or less toxic side effects for people who rely on those medicines.

    Constant improvements in purity and consistency have a knock-on effect downstream. Researchers save time, costs drop, and complicated reactions become part of daily procedure instead of something reserved for specialist centers. In my own work with medicinal chemistry teams, I saw the difference between chasing contaminants for weeks and getting reproducible outcomes because the starting materials did their job.

    This reliability also keeps projects running on schedule, which makes a real impact in time-sensitive drug development or innovation races in materials science. Scientists don’t just want something that can work in theory; they need it to work every time, and compounds like 7-Bromo-2,3-Dihydro-Isoindol-1-One carry that expectation.

    Challenges and Obstacles: Pushing for Better Solutions

    No production process hits perfection day one. With organic compounds, scaling up from research batches to industry-sized runs always exposes weaknesses. Quality drift, lot-to-lot variability, and environmental concerns come up, especially when hazardous bromine sources are part of the mix. Not every facility manages the risks well, and that matters when you consider the impact on workers and the planet.

    Managing hazardous waste, ensuring safe handling of brominated intermediates, and keeping up consistent analytical procedures all call for a high standard of responsibility. Top-tier manufacturers adopt closed-system synthesis, invest in air and water purification, and automate process monitoring. Regulatory agencies care deeply about how these chemicals move through the supply chain—honest traceability and full documentation are as much a part of the product as the compound itself.

    I’ve seen what happens when corners get cut: failed reactions, workplace hazards, and batches that have to be scrapped at great expense. Reputable suppliers push for faster detection of contaminants and digital tracking methods. They train technicians, update hazard labels, and keep compliance records ready for inspection. Sometimes this adds a little to cost, but the savings show up quickly—less downtime, lower waste, and safer labs.

    Supporting Evidence: Real-World Adoption

    Industry leaders and academic labs have made 7-Bromo-2,3-Dihydro-Isoindol-1-One a staple. Peer-reviewed articles document its use in postdoctoral research and published patents track its modifications for new drug candidates or material applications. The compound has appeared in well-known organic synthesis journals, particularly in schemes involving coupling reactions and late-stage functionalizations. It is referenced in studies on modulators for neural receptors and molecular scaffolds for enzyme inhibitors.

    Looking at market trends, companies have introduced automated systems to handle hazardous brominated intermediates, a move reflected in more consistent product data and safer processes. This level of transparency builds trust in scientific supply chains. Buying from sources that regularly post batch analytical data and undergo third-party certification helps avoid disruptions once a process moves toward the commercial stage.

    If you’re considering venturing into synthetic chemistry, you’ll find 7-Bromo-2,3-Dihydro-Isoindol-1-One available through established chemical suppliers, each listing thorough data sheets, standard pricing per gram, and technical support lines. While that sounds routine, the real advantage comes from users sharing feedback on yields, purity, and compatibility with various catalysts or solvents. This growing body of experience gives new users confidence and shortens the learning curve.

    Paving the Road Ahead: Innovations and Improvements

    No field stands still. As sustainable chemistry gains ground, producers are looking into greener production routes for 7-Bromo-2,3-Dihydro-Isoindol-1-One. Catalysts that work under milder, safer conditions garner strong interest, as do bio-based brominating agents or electrochemical methods that cut down on harsh chemicals. Some groups now pilot continuous-flow setups that further reduce exposure and waste. These upgrades don’t just improve lab safety—they’re part of the bigger effort to align chemical innovation with environmental goals.

    Quality control grows more sophisticated each year. Portable spectrometers, AI-assisted process monitoring, and better purity benchmarks make their way even into mid-sized labs. It’s not a luxury anymore—it’s how companies stay competitive in a market that prizes reliability and regulatory compliance. The net result shows up everywhere products derived from these compounds are used—from drug discovery to electronics.

    You can also spot innovation on the usage front. Medicinal chemists look at compounds like this and imagine two or three synthetic steps ahead, leveraging not just the bromine handle, but the rigid backbone for novel drug concepts. As new catalytic reactions make the rounds, accessibility to reliable starting materials delivers more options for laboratory teams looking to build complexity in fewer steps. Every shortcut matters, especially under tight R&D deadlines or limited funding.

    Potential Solutions for Ongoing Issues

    Challenges remain. Unwanted side reactions, environmental controversies around brominated waste, and supplier variability still rise to the surface. The solutions, though, come from realistic collaboration between scientists, manufacturers, and regulators.

    Better process controls provide one layer of defense. Standardizing synthesis routes, monitoring for trace contaminants, and exchanging best practices among manufacturers can keep quality high. Those of us who’ve run reactions night after night know how tempting it feels to trust a familiar supplier or method—but peer review and external audits help catch blind spots. Bringing in third-party validation gives customers tangible proof that a lot meets stated specs.

    Pushing for greener chemistry fits, too. Changing the reagents, swapping solvents, or adopting processes that recover and retard waste bromine make a big difference. Several suppliers report on efforts to cut overall process mass intensity (PMI), a number that tracks the total amount of material needed to make a kilogram of compound. That figure speaks volumes about efficiency and sustainability, and industry reports show real progress in reducing environmental burdens.

    Users could also tap into online communities of chemists and engineers. These platforms have moved past casual chatter—they now host discussions on optimizing yields, solving scale-up puzzles, and troubleshooting difficult purifications. A single shared protocol or test result can shave weeks off method development. Over time, the collective expertise helps everyone raise their standards.

    Improved transparency matters just as much. Suppliers sharing batch-specific data sheets, certificates of analysis, and even anonymized user feedback make it easier to select the right lot for a given project. Some companies now provide digital dashboards where buyers check recent quality stats in real time before placing an order. Reducing the guesswork protects both budgets and timelines.

    Lessons from Experience: What Works Best

    Having spent time in research and at the scale-up interface, I know not every fancy molecule lives up to its promise. But well-characterized intermediates like 7-Bromo-2,3-Dihydro-Isoindol-1-One power a lot of incremental, unseen progress. No newspaper will headline the creation of a pure batch, yet that hard-won consistency makes downstream breakthroughs possible.

    What stands out most is this: reliability built on scientific rigor, open communication between buyers and producers, and a willingness to adapt as technology advances. In a field where the tiniest contaminant can torpedo months of work, robust supply chains and honest dialogue about specifications, sustainability, and application data do more for end-users than any marketing claim.

    With the chemistry world moving faster and demanding more, the value of a compound comes from more than just its reactivity. It’s about how many headaches it avoids, how it takes one step off a multi-step journey, and how smoothly it gets to the people who need it. 7-Bromo-2,3-Dihydro-Isoindol-1-One brings those practical benefits into cutting-edge labs, established factories, and, eventually, real-world products. That’s what progress looks like in action—and compounds like this quietly drive it forward.