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HS Code |
555570 |
| Compound Name | 6-bromo-4-oxo-4H-chromene-3-carbaldehyde |
| Molecular Formula | C10H5BrO3 |
| Molecular Weight | 253.05 g/mol |
| Chemical Class | Coumarin derivative |
| Cas Number | 1272420-26-2 |
| Appearance | Yellow solid |
| Melting Point | 201-205°C |
| Solubility | Slightly soluble in organic solvents |
| Boiling Point | Decomposes before boiling |
| Smiles | O=Cc1c(Br)ccc2c(=O)occc12 |
As an accredited 6-bromo-4-oxo-4H-chromene-3-carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 10g amber glass bottle with a sealed cap, labeled "6-bromo-4-oxo-4H-chromene-3-carbaldehyde," includes safety and storage information. |
| Container Loading (20′ FCL) | 20′ FCL loaded with securely packed drums of 6-bromo-4-oxo-4H-chromene-3-carbaldehyde, ensuring safe and contamination-free transport. |
| Shipping | The chemical **6-bromo-4-oxo-4H-chromene-3-carbaldehyde** is shipped in a tightly sealed, chemical-resistant container to prevent moisture and light exposure. It is transported in compliance with relevant hazardous material regulations, using appropriate labeling and documentation. Temperature control and handling instructions are provided to ensure safe and secure delivery to the destination. |
| Storage | 6-Bromo-4-oxo-4H-chromene-3-carbaldehyde should be stored in a cool, dry, well-ventilated area, away from direct sunlight and sources of ignition. Keep the container tightly closed and protected from moisture. Store separately from incompatible materials such as strong acids, bases, and oxidizers. Use appropriate chemical-resistant containers and ensure proper labeling for safety and easy identification. |
| Shelf Life | 6-bromo-4-oxo-4H-chromene-3-carbaldehyde is stable for at least 2 years if stored cool, dry, and protected from light. |
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Purity 98%: 6-bromo-4-oxo-4H-chromene-3-carbaldehyde with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and minimal by-product formation. Melting Point 210°C: 6-bromo-4-oxo-4H-chromene-3-carbaldehyde with a melting point of 210°C is used in solid-phase organic synthesis, where thermal stability enables robust process control. Molecular Weight 281.05 g/mol: 6-bromo-4-oxo-4H-chromene-3-carbaldehyde with a molecular weight of 281.05 g/mol is used in medicinal chemistry research, where precise stoichiometric calculations enhance reproducibility. Particle Size <50 µm: 6-bromo-4-oxo-4H-chromene-3-carbaldehyde with particle size less than 50 µm is used in tablet formulation, where uniform particle distribution improves dissolution rates. Stability Temperature up to 120°C: 6-bromo-4-oxo-4H-chromene-3-carbaldehyde with stability temperature up to 120°C is used in high-temperature catalytic reactions, where maintained structural integrity supports prolonged process durations. |
Competitive 6-bromo-4-oxo-4H-chromene-3-carbaldehyde prices that fit your budget—flexible terms and customized quotes for every order.
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For years, our team has worked directly with research scientists, pharmaceutical developers, and industrial chemists who push boundaries and drive discovery. Every time we prepare a batch of 6-bromo-4-oxo-4H-chromene-3-carbaldehyde, it isn’t just another day’s work for us. Crafting this compound means blending precision, deep knowledge of chromene chemistry, and respect for strict standards that matter to those at the frontlines of synthesis and innovation. We understand how crucial purity and consistent performance are in your work, both in labs and at production scale. This specific chromene derivative presents unique reactivity, and every step—right from controlled bromination to crystallization—demands expert attention that comes with years on the manufacturing floor, not just reading technical manuals.
There is a common misconception in specialty chemical circles: that all chromene-aldehyde compounds behave similarly or that minor differences in molecular structure seldom impact project outcomes. From direct experience, this is simply not true. The introduction of a bromine atom at the 6-position fundamentally shifts the electron distribution across the chromene backbone. We see the effects firsthand in oxidation states and subsequent compatibility with a range of coupling partners. Teams engaged in medicinal chemistry or advanced material synthesis often come to us after discovering so-called “generic” batches lack the clean, validated profiles they expect. Inconsistent byproduct levels, high color impurities, or problematic moisture content can sideline weeks of planned research. This is why we don’t chase short-term savings by cutting corners or passing off partially finished goods. Instead, every production cycle is designed for carefully measured reaction conditions, tightly controlled solvent selections, and final verification against benchmarked NMR and HPLC results.
Feedback from synthesis labs speaks to the importance of robust, traceable supply chains. We draw from this feedback by using only documented precursor lots, and our managers oversee every transfer before and after each process. Our approach does not rest on automation alone. We have learned that manually monitoring certain stages, like the slow addition of brominating agents, reduces the risk of unwanted dibromo byproduct formation and provides greater assurance that final products meet the high threshold required by your protocols.
After the initial bromination, our team conducts stepwise purification, using solvent crystallization techniques tailored to this molecule’s unique solubility profile. Some have tried using standard silica or carbon treatments, but we have repeatedly found these methods introduce batch-to-batch variance. Our adapted crystallization protocol, recorded and refined over dozens of runs, has consistently led to reproducible quality—free-flowing, uniformly pale yellow solid, verified for single-phase composition each time. Routine checks ensure low halide residuals and tight control over aldehyde reactivity, protecting downstream reactions against unwanted side processes.
We don’t simply rely on instrument readouts, even though we have strong analytics. This practice dates back to our earliest days, where a senior chemist would “read” the crystalline habit of new batches. Many in our crew have spent decades on the line, learning not just chemical recipes, but also handling, packing, and even troubleshooting unforeseen shifts in humidity. These details matter; they show up as fewer customer complaints and minimal rework cycles. It’s real-world skill, not just lab protocol.
6-Bromo-4-oxo-4H-chromene-3-carbaldehyde is not a commodity intermediate. It serves in a range of complex synthetic pathways. Among our customers, research units frequently use it as a precursor for constructing fused heterocycles—key motifs in both antimicrobial agents and certain dye compounds. Being on the front lines, we’ve observed numerous project teams express frustration after ordering from outside brokers or repackers. These sources often prioritize bulk turnover and cut corners in documentation, leaving chemists guessing at the true reactivity and impurity profile of what lands on their benches.
People who reach out to us rarely just want a “standard” product. More often, we field questions on precise melting points, solubility in mixed ethers, or behavior under specific coupling catalysts. We prioritize these needs. Every lot leaves our facility with tightly aligned purity & moiety verification, so you don’t need to waste time on extra preps, distillations, or unwanted side product cleanups. It’s easier to trust your experimental data when your compound starts pure, behaves predictably, and leaves no doubts about its structure.
Our technical team keeps open logs of measured melting temperatures, detailed NMR spectra, and water content by Karl Fischer. Since the majority of our customers work in IP-sensitive spaces, we never share proprietary processing routes, but we do provide up-to-date, lot-specific supporting documents to reduce the load on your incoming QC. If researchers discover a deviation or have unique formulation constraints, they know they can call direct. We collaborate on custom purification or offer microbatches for pilot studies. This partnership mentality stands in sharp contrast to the inflexible catalog mentality seen elsewhere.
One of the clearest signals we see is the role of 6-bromo-4-oxo-4H-chromene-3-carbaldehyde in expanding chemical libraries. Because its aldehyde group sits at the 3-position, it opens up convenient access to Schiff base formation, enamine construction, and library expansion in fragment-based drug discovery. The robustness of the bromo substituent supports further functionalization, where selectivity matters for precision in final target design. Our product sees frequent use where teams need to construct elaborate cores for kinase inhibitor screens or advanced analogs of coumarin dyes.
Early on, we learned this compound challenges some common practices. Less experienced handlers often store it in uncontrolled environments, risking slow polymerization or hydrolysis. We addressed this risk by providing detailed storage guidance—dry, airtight conditions with light-exclusion packaging. We have seen the difference this makes. Returns and complaints from spoiled batches have dropped to near zero since the rollout of improved moisture-guard containers and photo-protective wraps. These tweaks aren’t always reflected in spec sheets but shine through in user satisfaction.
We maintain a direct feedback loop. When problems arise, such as unexpected side reactions or solubility mismatches in certain solvent blends, it reaches us quickly. Sometimes, these incidents require revisiting our processing, shifting the final drying protocol, or adding a secondary sieve step. We do this work not because a buyer demands it, but because as the manufacturer, our name and our people stand behind every shipment, and we know our own production systems better than anyone. Stories of failed reactions or contaminated reference batches push us toward further improvement.
Chromene-based intermediates surround this structure, making fine distinctions vital. Some users attempt substitutions with standard 4-oxo-4H-chromene-3-carbaldehyde, omitting the bromine. This route does not deliver the same results; halogenation can fundamentally alter the electronic properties. Through the years, we have performed side-by-side runs comparing brominated versus non-brominated analogs under Suzuki or Sonogashira conditions. Yields, product selectivity, and downstream scalability favor the targeted version in routes prioritizing cross-coupling extension or targeted medicinal modifications.
While there is a place for other halogenated variants—such as the chloro or iodo derivates—the 6-bromo version reflects a useful balance. Its reactivity often proves less aggressive than the iodine analog and more predictable than the chloro variant in protecting the aldehyde functionality. Our lines run structured experiments on these differences, beyond just what the literature outlines. Resulting process logs from synthetic scaleups highlight stronger batch reliability and fewer post-synthetic handling steps when starting from our 6-bromo-4-oxo-4H-chromene-3-carbaldehyde.
Over time, we have come to recognize a related challenge: many competitors, especially in reselling channels, blend lower-grade material or offer “chromene aldehyde” generically, failing to disclose precise substitution patterns. If a customer’s spec outlines an exact isomer, any mislabeling leads to costly setbacks—not just lost time, but actual failed experiments and wasted resources. Our labeling, lot tracking, and QMS (quality management systems) are set up so that errors are virtually impossible, and in case of any question, production flow can be traced back to the reactor source and operator record.
Anyone who has spent years in manufacturing understands that keeping promises on quality and reproducibility draws the line between a product trusted by industry and something that simply fills catalog space. As the manufacturer, we feel responsibility not just to fill orders but to serve the advancement of chemical science. Reproducibility isn’t an abstract target—every failed reaction out there can trace back to hidden impurities or poorly documented process steps. Whether shipped in gram or multi-kilogram lots, each product batch means a direct relationship with the result and reputation for accuracy.
What sets our product apart isn’t just our technical process, but the mindset we bring as hands-on makers. Many of us started on the bench and later moved through production and QC, carrying respect for the knock-on effects that small process changes bring. We keep logs on environmental swings, track solvent lots, and follow up with customers when an edge result appears. Solutions to unexpected situations flow fastest when there’s a foundation of trust between supplier and user—and we maintain that every day.
Technical support from a manufacturer means sharing more than just a COA. Our crew fields direct calls about non-standard dissolution, handling, and purification questions, drawing on everything from established protocols to real-world quirks encountered during scale-up. Some of our customers have processed thousands of multistep syntheses using our 6-bromo-4-oxo-4H-chromene-3-carbaldehyde; when minor issues come up—such as color shifts under nitrogen or retention time changes—we troubleshoot together, examining production logs and working toward a correction. There’s no bureaucracy or delay in addressing concerns, because our focus has never left the shop floor.
Chemical manufacturing carries the obligation to avoid exploitation—of people, of regulations, and of the planet. In crafting 6-bromo-4-oxo-4H-chromene-3-carbaldehyde, we apply strict stewardship in sourcing, production emissions, and workforce safety. Reports from labs and industrial users indicate that products sourced through “faceless” brokers may come with inadequate documentation regarding origin, heavy-metal contamination, or ethical labor. Our ties to our workforce extend decades, and every employee receives continuous training in safe handling, minimizing waste, and tracking improvements.
Moving toward green chemistry has shaped our approach. Solvent and reagent usage remain the two major sources of impact, so we spend real resources studying alternatives. Although some peers continue to rely on legacy processes, we invest in recycling, solvent recovery, and implementing lower-impact synthetic steps where possible. Our bromination step, often viewed as a generator of corrosive waste, now uses a scavenger-based capture tank, turning hazardous residues into manageable waste streams. We share summaries of progress as part of our sustainability transparency, not as a marketing ploy, but as a record of what can be done in real operation.
We believe manufacturing transparency also inspires end users, who can then have confidence in the upstream story behind the bench-level compound they receive.
What drives our production strategy isn’t just day-to-day output but awareness that chemists continually imagine new uses for established compounds. 6-bromo-4-oxo-4H-chromene-3-carbaldehyde has emerged as a linchpin in synthetic planning for many, yet every year brings new protocols and cross-coupling chemistries that add layers of complexity. Our technical service team participates in user forums and literature surveys, seeking out requests for new forms—perhaps finer particle sizing, or bulk-scale packaging for plant-based synthesis groups. We see firsthand that no “one size” fits all, and sometimes adopt custom microbatch protocols upon special request.
Our knowledge of handling isn’t theoretical. Years spent in bulk and fine chemical manufacturing tunes us to storage realities and global shipping: temperature fluctuations, regulatory differences, and handling during transshipment. These factors feed into our packaging design and guidance documents, which we update as supply chains evolve. If a user from a climate with large humidity swings asks for best practice, our advice draws on in-house data and customer experience, not outdated boilerplate.
Feedback from applied labs underscores how vital it is that documentation comes clearly, quickly, and with direct links to the production event. Our technical staff respond with complete spectral and analytical data, recorded for every lot as a matter of responsibility. This expectation didn’t arise through regulator push, but through the lived experience of having researchers frustrated by gaps in technical documentation or incomplete traceability from other suppliers.
Stepping back, it’s worth recognizing that 6-bromo-4-oxo-4H-chromene-3-carbaldehyde produces more than scientific value. It represents knowledge accumulation, the fruits of constant process improvement, and the care we invest in every batch. From carefully planned reactor setups through final drying, packaging, and real-world technical support, our focus stays fixed on quality and user trust. Every grain and every container links back to the efforts of skilled staff, rigorous in-process controls, and a spirit of partnership with researchers worldwide.
As demand grows for complex intermediates, the future will call for even tighter standards—not just for product quality, but for ethical conduct and environmental stewardship. We take this challenge personally and see it as an ongoing responsibility. Our story is written not by marketers but by skilled chemical workers and technical staff proud of their part in supporting scientific advancement through reliable, transparent, and respectful manufacturing.