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HS Code |
861266 |
| Productname | 6,8-Dichloro-3-Cyanochromone |
| Casnumber | 94449-77-9 |
| Molecularformula | C10H3Cl2NO2 |
| Molecularweight | 240.04 g/mol |
| Appearance | Light yellow solid |
| Meltingpoint | 220-224°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in organic solvents (e.g., DMSO) |
| Storagetemperature | Store at 2-8°C |
| Synonyms | 6,8-Dichloro-3-cyan-4H-1-benzopyran-4-one |
| Smiles | C1=CC(=C(C2=C(O1)C(=O)C(=C(C2)Cl)C#N)Cl) |
| Inchikey | AUIRQYOVZMGSSE-UHFFFAOYSA-N |
As an accredited 6,8-Dichloro-3-Cyanochromone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 5 grams of 6,8-Dichloro-3-Cyanochromone; labeled with chemical name, CAS number, and hazard symbols. |
| Shipping | 6,8-Dichloro-3-Cyanochromone is securely packaged in sealed, chemical-resistant containers to prevent leakage and contamination. The shipment complies with relevant safety regulations, including labeling for hazardous chemicals if applicable. Transportation is conducted via approved carriers, ensuring controlled temperature and environmental conditions to maintain product integrity throughout delivery. |
| Storage | Store 6,8-Dichloro-3-Cyanochromone in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Keep away from incompatible substances such as strong oxidizers. Use only in a chemical fume hood. Ensure proper labeling, and avoid moisture exposure. Follow all relevant safety and local storage regulations. |
Applications of 6,8-Dichloro-3-Cyanochromone in Industrial Manufacturing6,8-Dichloro-3-Cyanochromone enables specialized synthesis routes in multiple chemical sectors. We supply this intermediate to global manufacturers for targeted process applications with strict controls on quality, compliance, and integration. 1. Pharmaceutical Intermediate for Anti-Inflammatory Drug SynthesisMany pharmaceutical manufacturers employ this chromone derivative in the synthesis of non-steroidal anti-inflammatory drug (NSAID) candidates, specifically in heterocyclic compound construction steps. It acts as a building block for pyranone-based scaffolds, which are commonly used in research and production environments for proprietary drug molecules under clinical evaluation. Controlled handling and traceability are essential throughout the process. Strict impurity profiling and batch documentation occur at every stage to meet regulated pharmaceutical standards, from pilot to commercial-scale production. Industry compliance standards
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2. Agrochemical Intermediate for Heterocyclic Herbicide SynthesisFormulators in the agrochemical sector use this material in the assembly of heterocyclic herbicidal actives. Its halogenated, cyano-functionalized chromone structure makes it a valued precursor for generating selective inhibitors targeting weed metabolism, by participating in key cyclization or condensation reactions. Quality and environmental compliance remain strictly monitored, especially due to regulatory scrutiny of trace organochlorine levels throughout the downstream operations and end-use evaluation under agrochemical field conditions. Industry compliance standards
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3. Dye and Pigment Intermediate for Performance CoatingsProducers of specialty dyes and pigments integrate this compound for constructing chromophore cores in advanced colorants, especially for high-performance or weather-resistant applications. The substituent pattern on the chromone ring enables synthesis of halogenated or cyano-functionalized pigment molecules exhibiting strong UV stability, lightfastness, and chemical inertness. Feedstock qualification and process documentation adhere to strict color industry quality frameworks, particularly for products used in industrial or architectural coatings. Industry compliance standards
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4. Specialty Polymer Modifier for Optical MaterialsManufacturers of specialty polymers for optical and electronic applications use this compound as a modifying agent to introduce halogen and cyano substituents into copolymer chains. Its molecular structure allows precise adjustment of refractive index, thermal stability, and compatibility in advanced film or lens materials. Manufacturers tightly control conditions to minimize incorporation of process impurities, and maintain batch uniformity to support high-precision downstream forming, extrusion, or molding. Industry compliance standards
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Working every day in our chemical synthesis facility, one quickly learns the importance of a reliable intermediate like 6,8-Dichloro-3-Cyanochromone. Organic chemistry seldom gives us shortcuts, so when a compound consistently shows high performance, both in yield and in reactivity, it simply becomes part of the backbone for future innovations. This molecule—recognized for its two chlorine atoms at the 6 and 8 positions of the chromone ring and a cyano group at the 3 position—offers a one-of-a-kind blend of electron-withdrawing power and synthetic flexibility. In practical terms, we manufacture this compound to be the workhorse for both research and industrial labs targeting advanced pharmaceutical frameworks, new fluorescent markers, and specialty agrochemical intermediates.
Demand for this compound isn’t driven by marketing spin. It’s the result of push and pull in real research and batch production. From a synthetic chemist’s perspective, its dichloro substitution pattern leads to selective functionalization, which means downstream modifications take place where you want them. The cyano group, valuable in itself, enables strong nucleophilic additions and cycloaddition reactions, making the molecule suitable for custom heterocycle design. Colleagues in medicinal research especially value this intermediary step for crafting kinase inhibitors and anti-viral compounds. In our experience, the push for selective, reproducible reactivity continues to grow, and this molecule handles that job when others fall short.
Lab teams appreciate 6,8-Dichloro-3-Cyanochromone because it holds up during multi-step syntheses, thanks to its thermal and hydrolytic stability. The compound resists unwanted side-reactions under normal lab conditions and avoids decomposition during routine solvent evaporations. We noticed this first hand while scaling up for a project where trace impurities in lower-quality intermediates hindered crystallization on scale. Our setup, controlling for critical process parameters—temperature profile, solvent quality, efficient agitation—helps deliver material with high purity, low residual solvent, and minimal by-products. It’s impossible to underestimate the time savings when operators don’t face crystallization bottlenecks or purification setbacks caused by unstable intermediates.
Scalability and traceability define modern manufacturing. In our plant, every batch of 6,8-Dichloro-3-Cyanochromone runs through closely monitored reactors. Operators track time, temperature, and pressure by the minute. A dedicated analytical team tests every stage: after ring closure, after work-up, after isolation. Final lots routinely reach purities of 98.5 percent or higher by HPLC, with specific organic impurities quantified each time. No corners get cut—because repeat orders come from labs that expect repeat results. Years of feedback taught our crew that trace contamination can wreck specialized biochemistry assays downstream, so we keep analytical records and share them with every shipper.
Rather than list off a narrow set of presentation forms, we focus on how the product behaves in the field. Dusty, poorly formed solids slow down sample preparation or alter how a chemist measures their stock. So, our facility relies on robust filtration, drying, and controlled milling to produce a crystalline product with excellent flow and easy weighability. NMR and HPLC data, matched against reference standards, confirm structure and purity on every lot. Moisture content consistently stays below 0.5 percent, since higher values tend to compromise performance in anhydrous reactions such as lithiation or Grignard additions.
Chromone derivatives fill a wide space in organic synthesis, but swapping methyl or nitro groups for dichloro and cyano substitutions brings out big shifts in both reactivity and downstream design. The presence of two chloro groups on the chromone ring creates more potent electron delocalization, letting researchers direct further functionalization with a degree of site selectivity that a plain chromone or mono-chloro variant can’t match. Once the cyano group comes into play, the molecule transforms into a building block for more complex heterocyclic motifs. These substitutions permit the fine-tuning of biological activity or the adjustment of photophysical properties in fluorescent probe work.
From direct conversations with medicinal chemistry groups, plain chromone or mono-chloro substituted intermediates force extra synthetic steps to reach functional targets. The dichloro-cyano pattern cuts out tedious protection/deprotection steps. Productivity increases, overall cost drops, and fewer side products need to be purged. This one reason, among many, is why reaction design across the industry gravitates toward this compound for rapid lead optimization campaigns.
Companies that put short term gain over long-term trust tend to fade and leave messes for others. In practice, our handling of 6,8-Dichloro-3-Cyanochromone matches the expectations of customers focused on environmental stewardship and regulatory compliance. Waste streams, especially those involving halogenated by-products, get thorough treatment. Licensed contractors handle high-chloride sludges, and in-house oxidizers break down mother liquors before release. In the plant, our ventilation and personal protective gear match rigorous internal protocols, based on periodic industrial hygiene review, to limit employee exposure to any potentially harmful vapors or particulates. Stringent record keeping and batch segregation make audits routine and reassure clients about supply chain integrity.
Experience counts when you hit scale-up obstacles: solubility spikes, filtration hurdles, exothermic phases. Our team faced stoppages more than once because a low-quality batch from a supplier led to filter press blinding or erratic color in the intermediate. Now, rather than gamble, we keep input raw materials under strict spec control and always conduct pilot-scale confirmation before swinging to large reactors. It’s a lesson that costs real time and money to learn, but it’s how reliable manufacturing turns from promise to reality.
Packaging operations also require hands-on attention. 6,8-Dichloro-3-Cyanochromone’s fine crystalline structure can generate static electricity, so our operators use grounded, sealed drums lined with anti-static bags. Regular training keeps accidents to a minimum, and every package receives visual and analytical checks for signs of transport stress or moisture ingress. These everyday safeguards prevent spoilage, cross-contamination, and regulatory headaches.
Not every batch ships without hitches, and admitting that up front keeps us critical and adaptive. Over the years, clients shared challenges like slightly off-color lots or unexpected melting behavior. These cues led us to improve crystallization endpoint detection and tweak post-synthesis drying temperatures. Lab colleagues at pharmaceutical partners reported difficulty dissolving some sub-batches in their chosen solvents, so we cross-checked for trace solvents or polymorphic transitions that could create dissolution obstacles. Each such feedback loop reshapes our SOPs, accelerating quality improvement for the next cycle. In an industry reliant on reproducibility, acknowledging missteps up front is the quickest route to respect and reliability.
Every process chemist knows that development doesn’t happen in a vacuum. Research collaborations, whether with university research groups or private R&D teams, often push the application envelope for 6,8-Dichloro-3-Cyanochromone. From our side, customization doesn’t just mean swapping a solvent or diluent. Real custom production means re-optimizing routes for scale, adjusting purification strategies to fit an academic group's analytical toolkit, or considering alternative synthetic starting materials when basic feedstocks face supply constraints. Through cooperative research agreements, our scale-up teams often consult directly with end users, streamlining transfer of technical knowledge and troubleshooting real-world hurdles.
Chemists in medicinal and materials R&D prize a rapid feedback loop. For this intermediate, we have found that hands-on support for pilot trials and detailed analysis of side products from downstream transformations give these relationships practical value. Customers design better molecules and we strengthen manufacturing with each cycle. It moves the industry forward when applied knowledge flows both ways.
Markets change overnight. In times of raw material shortages or political trade restrictions, customers worry about delivery stability. Over the last few years, disruptions in chlorinating agents and specialty solvents extended lead times and forced us to rethink our procurement strategy for precursors. We counteracted volatility by qualifying parallel supply routes and boosting on-site storage for vulnerable feedstocks. Investment in automated tank farms and temperature-controlled warehouse space helped us buffer against transport delays caused by unpredictable logistics or customs challenges. This multi-pronged approach keeps our output predictable and price spikes to a minimum, letting downstream users depend on readily available stock.
Export regulations around halogenated aromatics often tighten in key trade regions, so regulatory monitoring forms a pivot of our compliance program. International customers especially appreciate advanced notification of documentation updates, helping their import teams process shipments with less delay. These stability measures only come from years of managing cross-border logistics and learning from shipping snags and regulatory setbacks.
The most exciting part of our work comes when a classic intermediate like this ends up powering a new field. Early in-house development focused largely on pharmaceutical leads and polymer precursors, but the molecule’s strong chromone backbone coupled with its unique substitution opened doors in optoelectronics and bioimaging research. University teams leveraged its photophysical attributes to test new dyes and fluorescent tags, adjusting conjugation length by connecting through the cyano group. We responded by enhancing analytical support—adding advanced spectroscopy and photostability testing to our in-house lab arsenal.
Recent internal studies explored metal-catalyzed couplings, using the dichloro substitutions for site-specific Suzuki or Buchwald reactions. This opened channels for custom analog synthesis, supporting drug discovery as well as materials science. End users experimenting with next-generation pesticides discovered that the reactivity profile of the dichloro-cyanochromone platform improved selectivity and environmental breakdown compared to older structures. Hearing about these wins reaffirms our sense of purpose and guides further investment in flexible manufacturing and analytical capabilities.
The path to more efficient chromone intermediate production lies in process simplification and greener chemistry. Our technical teams continually test alternate chlorinating agents and less hazardous cyano insertion strategies to cut production overhead and lower environmental impact. Each novel synthetic approach must safeguard the final molecule’s reliability, so we benchmark side by side with standard production runs. Recycling solvents and capturing by-product HCl gas for reuse in other site operations let us bring down the ecological footprint and support a more circular approach to specialty chemical manufacturing.
Broader industry partnerships are on the table, targeting mutual gains in waste minimization and knowledge transfer. Communicating openly about synthesis challenges—such as minimizing off-spec diastereomers during large-scale condensations—lets companies and academic labs align their efforts and develop new best practices. Knowledge sharing of this sort, focused on real results rather than generic claims, builds a more competitive and sustainable base for future intermediate development.
Tomorrow’s chemical landscape, shaped by stricter quality standards and sustainability pressure, will demand intermediates that do more than just fit into the process—they must perform better, generate less waste, and respond to both regulatory scrutiny and end-user needs. 6,8-Dichloro-3-Cyanochromone, shaped by years of practical lab experience and feedback from leading chemists, continues to evolve as a go-to building block. Our model of open dialogue, technical rigor, and environmental responsiveness positions us to serve researchers and production teams aiming higher. Daily challenges, from unexpected lab glitches to global transport disruption, remind us that chemical manufacturing is about people as much as molecules. The more we listen and learn, the more powerful and versatile substances like this chromone derivative become in pushing research and industrial progress forward.