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HS Code |
635964 |
| Chemicalname | 6-Chloro-2H-chromene-3-carbonitrile |
| Casnumber | 55792-38-0 |
| Molecularformula | C10H6ClNO |
| Molecularweight | 191.62 |
| Appearance | Light yellow to brown solid |
| Meltingpoint | 117-119°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Smiles | C1=CC2=C(C(=C1)Cl)OC=C2C#N |
| Inchi | InChI=1S/C10H6ClNO/c11-8-2-1-3-9-7(5-12)4-6-13-10(8)9/h1-4,6H |
| Storageconditions | Store at room temperature, keep container tightly closed |
As an accredited 6-Chloro-2H-chromene-3-carbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, tightly sealed with a screw cap, labeled with chemical name, purity, hazard pictograms, and handling instructions. |
| Container Loading (20′ FCL) | 20′ FCL: 6-Chloro-2H-chromene-3-carbonitrile is loaded in 25kg fiber drums, 9–11 MT net weight per container. |
| Shipping | 6-Chloro-2H-chromene-3-carbonitrile is shipped in tightly sealed containers to prevent contamination and moisture exposure. The packaging complies with chemical safety regulations, ensuring safe transit. It is typically transported via ground or air, labeled as a laboratory chemical, and accompanied by appropriate documentation and safety data sheets (SDS) for handling and emergency measures. |
| Storage | 6-Chloro-2H-chromene-3-carbonitrile should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect from direct sunlight, moisture, and sources of ignition. Ensure proper labeling and follow all applicable safety protocols. Use suitable personal protective equipment when handling to prevent exposure. |
| Shelf Life | 6-Chloro-2H-chromene-3-carbonitrile should be stored in a cool, dry place; shelf life is typically two years unopened. |
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Purity 98%: 6-Chloro-2H-chromene-3-carbonitrile with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high product yield and minimal impurities. Molecular Weight 189.60 g/mol: 6-Chloro-2H-chromene-3-carbonitrile at molecular weight 189.60 g/mol is used in organic synthesis reactions, where it provides precise stoichiometric calculations for reproducible results. Melting Point 127°C: 6-Chloro-2H-chromene-3-carbonitrile with a melting point of 127°C is used in controlled crystallization processes, where it enables consistent solid-state formulation. Particle Size ≤ 50 µm: 6-Chloro-2H-chromene-3-carbonitrile with particle size ≤ 50 µm is used in fine chemical production, where it allows improved dispersion and reaction kinetics. Stability Temperature Up to 150°C: 6-Chloro-2H-chromene-3-carbonitrile with stability temperature up to 150°C is used in high-temperature synthesis, where it maintains structural integrity and reactivity. Solubility in DMSO 20 mg/mL: 6-Chloro-2H-chromene-3-carbonitrile with solubility in DMSO 20 mg/mL is used in biological assay development, where it enables accurate dosing and homogeneous solutions. |
Competitive 6-Chloro-2H-chromene-3-carbonitrile prices that fit your budget—flexible terms and customized quotes for every order.
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Standing on the production side of the chemical industry, we’ve grown alongside demand shifts in chromene derivatives. 6-Chloro-2H-chromene-3-carbonitrile—a compound sometimes overlooked in discussions of chromene chemistry—continues to hold a solid place in pharmaceutical, agrochemical, and specialty chemical synthesis. Our own journey with this intermediate has brought a clear sense of its importance as well as common misconceptions about its structure, reactivity, and downstream uses.
Let’s get straight into what we have learned working with this molecule—and what makes it distinct among chromene derivatives that pass through our plants.
We produce 6-Chloro-2H-chromene-3-carbonitrile as a crystalline solid, focusing on stability and consistent quality. Decades in scale-up and process engineering have shown that color and physical homogeneity communicate a lot about the batch process. Our in-house model generally uses a manufacturing route where the chloro substituent is introduced with controlled halogenation, while the nitrile group comes through reliable nucleophilic substitution. Each run starts with high-purity starting materials, aiming for a purity not less than 99 percent by HPLC and crystallinity that holds under ambient conditions.
Moisture is kept below 0.5 percent by Karl Fischer titration because humidity can compromise storage and subsequent reactivity. Practical experience has demonstrated that this compound, with a melting point near 120–124 °C, does not lump or cake even during extended storage, provided it’s kept away from direct sunlight and moisture ingress. Chemists and engineers handling the material repeatedly confirm that the product pours freely from drums and bags, minimizing downtime during transfer and weighing operations.
Monitoring crystal morphology with regular in-process checks reduces unwanted fines (powdery fractions), which can complicate both weighing accuracy and filtration when clients use the material for synthesis. Packaged in fiber drums with double polyethylene liners, our product stays dry and easy to handle, whether the destination is a pharmaceutical pilot plant or a bulk agrochemical production site.
Most requests for 6-Chloro-2H-chromene-3-carbonitrile flow in from fine chemical manufacturers and pharmaceutical companies with multistep syntheses on their line cards. The nitrile function at the 3-position of the chromene ring opens paths for further modification—converting it to amidines, carboxamides, or acids. We have seen clients carry it forward in routes leading to benzopyran-based pharmaceutical candidates, leveraging the electron-withdrawing chloro group to drive regioselectivity in subsequent reactions. Agrochemical researchers frequently look for this intermediate as part of building blocks for new insecticides or fungicides.
During our technical exchanges, some process chemists point out that the stability of this compound allows for more aggressive conditions in subsequent steps (like Grignard reactions or cyclizations) without degrading or leading to side products. Others appreciate that the product leaves little residue during evaporation, reducing the need for repeated recrystallization or flash chromatography. We’ve heard from several labs that it dissolves readily in DMF, DMSO, and chlorinated solvents, speeding up reaction set-up times on both small and kilo lab scales.
Years of feedback from clients have taught us that supply reliability and consistent performance trump minor fluctuations in price. Missed deliveries or color changes in the product lead to production headaches and downtime. So, we keep our focus on robust process control, timely shipment, and fielding technical questions directly from chemists at the bench—never passing them off to layers of intermediaries.
Having manufactured a range of halogenated and nitrile-containing chromenes, we have a firsthand sense of the subtle but crucial differences that affect application. Users often compare 6-Chloro-2H-chromene-3-carbonitrile with its bromo- and fluoro- analogs, as well as with unsubstituted chromene-3-carbonitrile. We see diverging downstream performance in cross-coupling reactions: the chloro version extends shelf life and displays different reactivity compared to bromo analogs, and it often comes with a more accessible price point thanks to lower raw material and process costs.
Chloro substituents bring a unique balance—providing suitable activation for nucleophilic aromatic substitutions, yet offering resistance to hydrolysis in water-sensitive environments. The fluoro analog sometimes performs even better in electronic modulation, but the production complexity and raw material sourcing for the fluoro version tend to push it into the costlier bracket—not to mention the handling precautions demanded by some fluorinated intermediates.
Comparing the chloro derivative with the parent chromene-3-carbonitrile, users often overlook the impact of added halogen. Over dozens of campaigns, our own team has confirmed that the 6-chloro product crystallizes out more cleanly, reducing the need to use anti-solvents or extended cooling. Downstream purification thus becomes simpler, with fewer yield losses—facts that matter to any chemist watching margins and production schedules.
In catalytic reactions (such as Suzuki or Buchwald-Hartwig couplings), the presence of the 6-chloro group slightly shifts selectivity and rate profiles. We see R&D groups favor this compound for trial runs that demand easy access to multiple derivatives from a single intermediate. Our technical support often receives requests for process optimization advice at this step—another reason to build supplier relationships with those who actually understand the chemistry at the production level.
Every kilogram of 6-Chloro-2H-chromene-3-carbonitrile begins with tight control over each reaction stage. Process engineers and QC chemists in our team maintain systems that track batch genealogy, starting from base reagents through finished packaging. We track not just purity and residual solvent content, but also batch-to-batch variability in melting point, particle size distribution, and color—all variables that can affect performance in synthesis.
When we troubleshoot plant operations, our history with this compound helps. For example, incomplete conversion during halogenation returns off-color or oily products, while trace acid contamination in final crystallization results in unwanted impurities that may only appear several steps downstream. Our QC labs continuously update impurity profiles so clients can anticipate potential purification strategies if their applications demand higher than usual product performance.
Transportation and storage bring their own challenges. International clients sometimes receive material stored for months in transit; products must remain stable in heat and humidity found in container shipping lanes. We test retained samples from older batches, checking for changes in assay, appearance, and moisture content. Shipping in lined drums guards against contamination and moisture pickup, especially during summer months.
Scaling up this compound from lab-bench to metric ton quantities is not a copy-paste task. On the plant floor, solvent recovery, waste stream handling, and reaction exotherms must all be balanced. It’s one thing to run a clean reaction at 5 grams; at 500 kilograms, cooling jacket performance, reactor reliability, and vacuum system health all come into play. We’ve seen that glass-lined reactors support longer campaigns and reduce metallic contamination, improving downstream crystallization and color.
Nitrile-containing molecules can present their own set of handling challenges. Safety protocols require proactive ventilation and real-time monitoring—not only for production staff safety but also to prevent cross-contamination with other chromene derivatives in our suite. After years of handling, we’ve optimized cleaning cycles to minimize downtime between campaigns, maintaining reliability and reducing maintenance costs.
Customers sometimes ask about greener synthesis routes or alternative solvents. While full solvent exchanges remain challenging at commercial scale, we’ve made gradual improvements—optimizing recycle ratios, recovering high-boiling solvents, and reducing halide waste through distillation. The drive for improved environmental performance fits squarely with industry movement toward more sustainable chemistry, but it takes continuous investment and a readiness to experiment.
With 6-Chloro-2H-chromene-3-carbonitrile’s frequent role as a pharmaceutical starting material, compliance matters. Our approach draws from repeated site audits by global customers who require full traceability and consistent documentation. Each batch leaves our site with a certificate of analysis, supported by spectral and chromatographic data interpreted by on-site chemists. All critical control points are recorded to support customer registration documents and filings.
Staff training forms the core of robust compliance; hands-on experience and a culture of transparent reporting catch deviations early. Internal audits and supplier reviews extend our risk management, especially when raw material volatility threatens seamless supply. The team’s daily commitment to documentation and process review ensures continuity, even across challenging production cycles in volatile supply chains.
We look for every opportunity to integrate client perspectives into our product refinement. Customer questions about trace impurities, alternative milling, or bulk packaging have directly informed changes on our shop floor—whether it means introducing a denser grade for higher-throughput processors or developing larger package sizes for single-batch dissolutions. These changes rarely happen overnight but grow out of repeated technical dialog with partners who are as invested in process excellence as we are.
The practical challenges that users face—such as bottlenecks during transfer, humidity pickup, or downstream filtration—help us adapt manufacturing routes, logistics, and packaging formats. Many improvements stem not from theoretical lab work but from close listening to working chemists, packaging staff, and R&D managers.
Our operational philosophy emphasizes a collaborative approach, where technical sales understands both plant operations and lab-scale applications. Every detail, from loading drums to optimizing final drying conditions, reflects a daily commitment to practical chemistry, cost-effective operations, and problem-solving.
There are advantages tied to sourcing directly from the actual manufacturer instead of intermediaries or traders. Robust manufacturing practices mean fewer surprises in batch-to-batch quality and specification. Questions about process history, impurity profiles, bespoke documentation, or tailored packaging get straight answers from people who actually made the compound—something that generic trading companies cannot offer.
Direct relationships build confidence, especially when project timelines stretch or regulatory demands increase. Our team has developed both the technical knowledge and operational discipline to troubleshoot unexpected issues, drawing on years of direct experience producing, testing, and delivering 6-Chloro-2H-chromene-3-carbonitrile for demanding industrial partners.
The close link between factory, technical support, and customer delivers more than just a specification; it provides context, solution pathways, and concrete guidance for any application challenges, from process optimization to compliance inquiries.
Reliable access to robust intermediates like 6-Chloro-2H-chromene-3-carbonitrile supports innovations in fields as varied as human health, crop protection, and materials science. While not every batch may go to blockbuster pharmaceuticals or headline agrochemical launches, every kilogram leaves our plant with the same discipline and attention to detail.
The stories we hear from our customers—from successful scale-ups to troubleshooting tough reaction bottlenecks—remind us that quality chemical manufacturing builds foundations for breakthroughs elsewhere. Daily dedication on the shop floor, transparent documentation, and technical dialog with clients keep the cycle of improvement moving forward.
As long as chromene chemistry keeps evolving, we stay committed to supporting every new challenge with practical know-how, robust quality, and reliable supply—one batch at a time.