|
HS Code |
203358 |
| Productname | 6-Chloro-3-Cyanochromone |
| Casnumber | 142137-16-6 |
| Molecularformula | C10H4ClNO2 |
| Molecularweight | 205.6 |
| Appearance | Light yellow to yellow powder |
| Meltingpoint | 205-208°C |
| Purity | ≥98% |
| Solubility | Slightly soluble in DMSO, insoluble in water |
| Storageconditions | Store at 2-8°C, away from light |
| Smiles | C1=CC2=C(C=C1Cl)OC(=O)C=C2C#N |
| Synonyms | 6-Chloro-3-cyan-4H-1-benzopyran-4-one |
As an accredited 6-Chloro-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 10 grams of 6-Chloro-3-Cyanochromone, sealed with a screw cap, labeled with hazard and identification information. |
| Shipping | 6-Chloro-3-Cyanochromone is shipped in tightly sealed, chemically resistant containers to prevent contamination and moisture exposure. It is handled as a hazardous material, with appropriate labeling and documentation per regulatory guidelines. The package is cushioned and secured to minimize breakage during transit and stored in a cool, dry environment. |
| Storage | 6-Chloro-3-Cyanochromone should be stored in a tightly sealed container, protected from light, moisture, and incompatible materials. Keep it in a cool, dry, and well-ventilated area, ideally in a chemical storage cabinet designated for hazardous organic compounds. Properly label the container and avoid sources of heat or ignition. Follow all relevant safety guidelines and local regulations. |
Applications of 6-Chloro-3-Cyanochromone in Industrial Manufacturing6-Chloro-3-cyanochromone serves as a critical intermediate in multiple high-value chemical synthesis processes. As an original manufacturer, we supply this material to downstream partners operating in complex pharmaceutical and agrochemical value chains. The following sections provide detailed insight into its established application scenarios, including compliance standards, industrial formulation practices, process steps, and resulting end products. 1. Synthesis of Antiviral Pharmaceutical Active IngredientsPharmaceutical producers integrate this raw material into multistep syntheses to construct antiviral drug candidates, particularly those in the chromone-derived naphthyridine or phenylpyrimidine classes. The electron-withdrawing groups on the molecule facilitate regioselective substitutions during later-stage transformations, which are crucial for generating advanced intermediates in API pathways. Partnering innovators rely on the high purity and trace impurity control we deliver to support their regulatory submissions. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Fungicide Intermediate ManufacturingIn crop protection chemical development, this compound occupies a central role as a building block for selective fungicide actives. Agrochemical formulators use its chemical structure to introduce halogenated chromone functionalities, giving the target molecules improved field stability and pest resistance spectrum. Integration into synthesis allows downstream partners to optimize for both activity and environmental persistence, essential for regulatory registration and performance claims. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Specialty Dyes and Pigment SynthesisProducers of high-performance dyes and pigments employ this chromone derivative to introduce controlled coloration and photostability into chemical formulations for plastics and synthetic fiber applications. The material’s unique substitution pattern allows chemists to manipulate absorption wavelengths during azo or anthraquinone dye synthesis, delivering final pigments with consistent hue, lightfastness, and process compatibility for technical textiles, coatings, and engineering plastics. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Fine Chemical Electronic Material IntermediateManufacturers of organic electronic intermediates rely on this compound to engineer electron transport layers and fluorescent chromophores in the fabrication of OLED materials. Its halogenated and cyano groups enable precise modulation of molecular energy bands, which is critical for downstream producers achieving the necessary electrical properties in thin-film electronics, optoelectronics, and specialty polymer blends used in advanced display technology. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 6-Chloro-3-Cyanochromone prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
There’s a long path between a raw chemical reaction and a trusted, well-made intermediate. Every batch matters. We know this from years spent navigating the practical realities of manufacturing pharmaceutically-relevant compounds. Among the aromatic heterocycles that land on our production floor, 6-Chloro-3-Cyanochromone holds a place of special interest for both R&D labs and process researchers. The reason is straightforward. Its molecular structure offers versatility, clean transformations, and a path toward a range of valuable substituted chromones, which serve as starting points for more complex bioactive molecules.
Our experience running different chromone derivatives on scalable lines showed early on that small differences in substitution patterns make a gigantic difference in downstream usability. For 6-Chloro-3-Cyanochromone, we learned that controlling the substitution at the 6-position with a chlorine atom gave a good balance between reactivity and manageability. The cyano group at the 3-position opens up reliable synthetic routes to further elaboration—nucleophilic addition, condensation, and reductions become far less troublesome than with many other cyano-bearing heterocycles.
It’s easy to overlook details in chromone chemistry if you aren’t watching a reactor or tuning the last filtration step. We manufacture 6-Chloro-3-Cyanochromone under careful batch protocols using proven solvents and crystallization sequences. Our process minimizes isomeric and impurity formation, maintaining a single isomer profile that matters a great deal downstream. The compound appears as a pale, off-white powder, with a melting point near 175-177°C under unaltered conditions.
Every shipment undergoes HPLC and NMR characterization. Those data sheets mean more than regulatory compliance—they mean fewer headaches for people depending on reliable material quality. Low single-digit moisture readings and consistent bulk density are not afterthoughts. In the years where customers struggled with sluggish dissolutions or tough purifications, we responded by digging into process development until the solid state and flowability met practical needs.
Based on our direct observations, the greatest risk isn’t in making 6-Chloro-3-Cyanochromone itself, but in keeping trace halides, incomplete condensation byproducts, and trace oxidizable impurities at bay. Early on, we realized our post-processing protocol needed streamlining, not just more washing steps. Introducing a more gradual crystallization and fine-tuned solvent removal allows the compound to separate cleanly and store more stably, even across seasonal temperature swings seen in bulk warehouses.
Pharmaceutical synthesis draws the lion’s share of interest for 6-Chloro-3-Cyanochromone. Its core skeleton frequently appears in intermediates for kinase inhibitors, anti-inflammatory leads, and molecules aimed at CNS and antiviral research. Customers in medicinal chemistry push for both purity and batch-to-batch reproducibility—requirements we take seriously. We’ve collaborated with clients on custom modifications and scale-ups, always seeking safer pathways and waste minimization.
Academic and industrial users frequently use 6-Chloro-3-Cyanochromone in Suzuki and Buchwald coupling chemistry. The chlorine at the 6-position acts as a robust leaving group, allowing functionalization with aryl, alkyl, or heteroaryl groups. The cyano group enables further manipulation into amidines, amines, or acids, supporting combinatorial approaches in drug discovery.
We’ve observed another benefit: compared to structurally similar intermediates, 6-Chloro-3-Cyanochromone undergoes substitutions cleaner, with less tendency toward rearrangement or overreaction at the chromone core. This matters in automated platforms, where side reactions create cleanup nightmares. Teams who run multi-step routes appreciate lowered purification burdens and fewer batch failures, particularly in early-stage API development where time is tight.
Several chromone intermediates cross our production lines: 3-formylchromone, 6-bromochromone, 6-fluoro-3-cyanochromone, and others. Differences among them aren’t academic; they shape cost, safety, and viability in a busy synthesis pipeline.
Chlorine offers unique value in our experience. Brominated analogs often demand higher-cost halogen sources and stronger bases in subsequent steps, which increases exotherm risks and harsher waste processing. Fluorinated versions, while potent in structure-activity studies, bring persistent handling complications (corrosive residues, tenacious impurities). The cyano group at the 3-position in our 6-Chloro-3-Cyanochromone remains more stable during storage and less prone to hydrolysis than the formyl or nitro analogs, which tend to degrade in moist or variable storage setups.
Handling characteristics set our product apart. Where many related chromones show tendency toward clumping or deliquescence—especially in humid environments—our improved drying and crystallization protocols render a much drier, less caking product. This has real knock-on effects in automated feeding, sampling, and metering systems. Less downtime. Fewer blocked hoppers. Over five years, these gains outpace whatever marginal cost advantages appear on initial quotes for less thoroughly processed material.
From a reactivity viewpoint: chlorinated intermediates yield higher selectivity and improved yields in common cross-coupling transformations—the backbone of modern medicinal chemistry. Using a less reactive halide often raises batch failure rates, while pushing to the highly activated brominated or iodinated systems increases cost and environmental scrutiny.
Safe chemical manufacturing hinges on more than a well-trained team and documented SOPs. Chromone derivatives bring their own process hazards—dust explosions, unsafe exotherms, or stubborn residual solvents. We learned early on that solvent choice, granule sizing, and real-time monitoring all play a part in taming these issues. Our analytical and engineering teams interface daily, keeping the plant floor running safer and tighter.
As for the environmental end, cyano- and chloro-substituted compounds demand careful waste treatment. We invested in in-house waste neutralization, closed-system solvent recovery, and regular air monitoring to stop halogen venting long before regulations caught up. The difference is practical: less regulatory downtime, minimized surprises at audit time, and an easier path for customers who rely on us for their own green chemistry goals.
We take questions of shelf-life and stability to heart. Products that degrade, clump, or lose loading percentages lead to unpredictable performance in downstream synthesis. That means more rework, more wasted material, and higher costs in the long run. Our stability data supports users tackling multi-month campaigns and multi-kilo scale-ups, delivering a dry, freely pouring product that’s reliable month after month.
Perfecting the chemistry of 6-Chloro-3-Cyanochromone isn’t just about optimizing numbers on a certificate. We re-engineered our route to reduce hazardous waste, cut high-energy feedstocks, and shift to greener workup technologies. The value here runs deeper than a marketing buzzword. We’ve watched as unsustainable or over-complex processes drive up both direct and hidden costs for clients—a problem compounded each year by regulatory tightening.
There’s pressure everywhere in the supply pipeline: customs changes, long delivery lead-times, periodic shortages of key raw materials. We buffer these risks with larger in-house raw feedstock inventories, diversified supplier relationships, and constant process documentation. Our investment in production flexibility means customers rely on us year-round without interruptions, a critical advantage for both pilot and manufacturing-stage partners.
Batches that deviate from spec aren’t shunted aside lightly. Internal traceability systems flag deviations immediately so rework occurs before discrepancies travel further downstream. Raw material certificates, process logs, and analytical data all stay linked to each lot number, serving as a backbone against recalls, regulatory review, or audit events. We see ourselves not just as bulk manufacturers but as stewards of users’ critical supply chains.
Working shoulder-to-shoulder with bench chemists and process development teams taught us: scale matters, but so does support. Many researchers need only small lots or timely access to pilot-scale quantities while evaluating new molecular series. For those users, we maintain stock for prompt turnaround, supported by full analytical packages and transparent, traceable batch histories.
Our technical team routinely answers process questions, offers alternatives for hard-to-source reagents, and suggests real-world tweaks learned in our own plants. Supporting users means more than selling; it means closing the loop between supplier and scientist, ensuring troubleshooting never stalls progress. Some clients request modifications—tailored crystallization forms, alternate particle sizes, or different stabilizing excipients. We collaborate closely, sharing pilot data and blending our own experience with customer targets.
Scaling up from lab flask to ton-scale output presented surprises at every stage. Heating and cooling rates, mixing, and filtration all demand recalibration. Chromone intermediates often resist easy translation from glassware to steel. We built larger pilot reactors with direct analog readouts for temperature spikes, and automated anti-solvent dosing to ensure repeatable, tight crystal size distributions. Adjustments like these came from real plant observations—lessons learned after watching minor changes tip whole batches out of spec.
Process shift from manual crystallization to semi-continuous operations meant training not just on procedures but on real-time troubleshooting. We built skills across our teams so everyone, from operator to line manager, understood both theory and plant-floor realities. It’s this broad-based investment in people as well as equipment that keeps 6-Chloro-3-Cyanochromone output consistently high quality year after year.
Market demand evolves as pharma R&D priorities shift. We keep improving our own methods—not just in the lab, but also in our logistics, sampling, and packaging teams. Sustainable packaging, dust-minimizing containers, and improved batch tracking came from customer suggestions, field experience, and our own troubleshooting.
In new application spaces, as chromone derivatives find their way into agrochemistry, dyes, and specialty material science, we adapt formulations to meet new performance metrics and regulatory requirements. This means partnership and iteration: sharing data, collecting feedback, and remaining agile in our production lines. It helps to look ahead, anticipate process pinch points, and build forward-looking capacity—so supply always keeps pace with emerging demand.
All of us on the factory floor, R&D benches, and loading docks know that real manufacturing wins come from detail and care, not shortcuts or empty assurances. Our approach to 6-Chloro-3-Cyanochromone flows from years of chasing higher purity, more stable product, and tighter process control. We see this as a commitment—not just to chemistry, but to every client building something new from our intermediates. It's not just about making molecules. It’s about building the trust that comes from consistent performance, open communication, and hands-on support.
As demand for high-performance heterocyclic building blocks continues to rise, our focus remains on the details that matter. A robust process. Reliable product every month of the year. Responsive support, whether a customer’s running analytical screens or full GMP-scale synthesis. That’s the benchmark we set, every batch, every shipment.