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HS Code |
797999 |
| Iupac Name | 6-fluoro-3,4-dihydro-2H-chromene-2-carboxylic acid |
| Cas Number | 1314469-97-4 |
| Molecular Formula | C10H9FO3 |
| Molecular Weight | 196.18 |
| Appearance | Solid (typically powder or crystalline) |
| Boiling Point | Decomposes before boiling |
| Solubility In Water | Slightly soluble |
| Smiles | C1C(OCC2=C1C=C(C=C2)F)C(=O)O |
| Inchi | InChI=1S/C10H9FO3/c11-7-2-1-6-4-8(10(12)13)5-14-9(6)3-7/h1-3,8H,4-5H2,(H,12,13) |
| Synonyms | 6-Fluoro-3,4-dihydrochromene-2-carboxylic acid |
| Pka | Estimated 4-5 (for carboxylic acid group) |
| Storage Conditions | Keep container tightly closed, store at 2-8°C, away from light and moisture |
| Hazard Statements | May cause irritation to skin, eyes, and respiratory tract |
As an accredited 6-fluoro-3,4-dihydro-2H-chromene-2-carboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 6-fluoro-3,4-dihydro-2H-chromene-2-carboxylic acid, securely sealed with tamper-evident cap. |
| Container Loading (20′ FCL) | 20′ FCL is loaded with securely packaged `6-fluoro-3,4-dihydro-2H-chromene-2-carboxylic acid`, ensuring safe transport and compliance. |
| Shipping | 6-Fluoro-3,4-dihydro-2H-chromene-2-carboxylic acid is shipped in tightly sealed containers to prevent moisture and contamination. The package is labeled according to chemical safety regulations and cushioned to avoid breakage. Standard shipping is by ground or air, compliant with local and international chemical transportation guidelines. Temperature control may be applied if required. |
| Storage | 6-Fluoro-3,4-dihydro-2H-chromene-2-carboxylic acid should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. The container should be tightly sealed and clearly labeled. Store the chemical at room temperature, protected from moisture, and isolated from incompatible substances such as strong oxidizers and bases to ensure stability and safety. |
| Shelf Life | The shelf life of 6-fluoro-3,4-dihydro-2H-chromene-2-carboxylic acid is typically 2–3 years when stored properly, protected from light. |
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Purity 98%: 6-fluoro-3,4-dihydro-2H-chromene-2-carboxylic acid with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reproducibility. Molecular weight 210.18 g/mol: 6-fluoro-3,4-dihydro-2H-chromene-2-carboxylic acid with a molecular weight of 210.18 g/mol is used in drug discovery, where it facilitates accurate dosage formulation. Melting point 152°C: 6-fluoro-3,4-dihydro-2H-chromene-2-carboxylic acid with a melting point of 152°C is used in solid dosage formulation, where it provides thermal stability during processing. Particle size <50 µm: 6-fluoro-3,4-dihydro-2H-chromene-2-carboxylic acid with a particle size less than 50 µm is used in suspension preparation, where it ensures uniform dispersion and enhanced bioavailability. Stability at 25°C: 6-fluoro-3,4-dihydro-2H-chromene-2-carboxylic acid demonstrating stability at 25°C is used in standard laboratory storage, where it maintains structural integrity over extended periods. Solubility in ethanol >10 mg/mL: 6-fluoro-3,4-dihydro-2H-chromene-2-carboxylic acid with solubility in ethanol greater than 10 mg/mL is used in analytical method development, where it allows for efficient sample preparation and processing. |
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Every batch of 6-fluoro-3,4-dihydro-2H-chromene-2-carboxylic acid that comes off our reactors represents years of accumulated experience not just in chemical synthesis, but in understanding what researchers and industrial partners demand from their intermediates. We approached its development not as another generic fluorinated compound, but as a solution where fluorine chemistry meets chromene stability—a combination needed more and more in both pharmaceutical and specialty chemical applications. Our lab teams handle schedules and raw material swings, yet keep the product tightly controlled batch after batch, which doesn’t happen by accident. There’s a lot that goes into bringing out the nuanced performance of 6-fluoro-3,4-dihydro-2H-chromene-2-carboxylic acid, and plenty that separates real manufacturer craftsmanship from a relabeled drum on a distributor’s shelf.
Chemists and process engineers who work with chromene derivatives already know the base system is a strong building block in medicinal chemistry. Introducing a fluorine at the six position, though, doesn't just tweak reactivity, it flips entire synthetic strategies. Fluorine’s electronegativity impacts metabolic pathways differently from hydrogen, chlorine, or methyl substitutions. In my own runs, this substitution demands careful attention to reaction conditions; it’s not just "throwing in a fluorine atom" as some catalogues would have you believe. The acidity, solubility, and compatibility with both water and organics change, opening up options for coupling that plain chromenes or chlorinated versions can’t offer. Pharma teams search out this compound for precisely these subtle differences—especially where fluorine can boost metabolic stability of final drug candidates or dial in just the right electronic push in a lead compound.
Specs matter. We focus on purity, particle form, and residual solvents because impurities can derail activity studies, or worse, invalidate expensive syntheses downstream. Our material gives consistent purity above 98 percent, as proven by not just HPLC but NMR and GC-MS on every production run. We keep the acid isolated as a solid rather than an oil, following experience gained from ruined polymerizations and failed crystallizations in the early years. Our analytical team found that particular care in the drying step reduced formation of esters or dimers, an issue sometimes seen in less controlled facilities using batch glassware instead of jacketed reactors with inline nitrogen sparge. The final appearance is a white to off-white powder that stays free-flowing and packs smoothly, a feature many clients praise when scaling up for kilo work or automated dispensing.
Direct manufacturing shortens the feedback path between real-world use and product upgrade. Over dozens of customer audits and process validations, we hear the same requests: transparency in crystal habit, granular control over sodium and heavy metal levels, and full traceability. Making the acid in-house means changes go live quickly—we can tweak reaction time, modify quench protocol, or try a new filter aid when a regular user reports an issue with solubility or downstream compatibility. Third-party sources often don’t have control over upstream synthesis or can’t offer rapid certificate updates. Every bottle we ship gets matched to a specific batch and backup sample held for five years, with COAs that don’t just state values, they show the raw data on microimpurities that medicinal chemists or regulatory teams might question.
We avoid routine cross-contamination by running dedicated lines for fluorinated intermediates, never relying on shared equipment used for nitroaromatics or alkylated compounds. Cleaning validations aren’t just a checkbox—they’re a daily habit, reinforced by surprise spot tests from QA and recorded at all operator turnovers. Fines in the powder get minimized by gentle milling under low shear, which my experience shows cuts down on dust (and inhalation risk) at the user’s end. These are invisible details to traders who handle drums, but in production, they’re the difference between a compound that integrates seamlessly and one that gums up your process line or throws off your yield calculations.
The primary push for 6-fluoro-3,4-dihydro-2H-chromene-2-carboxylic acid comes from drug discovery teams searching for improved bioactivity or stability. In our direct experience working with pharmaceutical R&D labs, this compound finds regular use in syntheses targeting CNS drugs, antivirals, and anti-inflammatories. Its fluorinated ring enhances metabolic resistance—this means medicines built from these scaffolds last longer in the body without rapid degradation, cutting down required dosing and improving patient outcomes.
Seasoned process chemists value the carboxylic acid group, which unlocks easy conjugation to amines, alcohols, and other nucleophiles. This acid function allows for diverse transformations—amide formation, esterifications, and Suzuki-Miyaura coupling—without needing to remodify the ring, saving precious steps and time. Teams scaling up pilot runs for active pharmaceutical ingredients care about the stability of the free acid; our process ensures this group remains intact and unesterified, which remains a point of difference versus certain commercial suppliers whose lots show significant impurity drift after a few months on the shelf.
Agrochemical developers, looking for new herbicide backbones or growth regulators, tap into the chromene’s unique reactivity profile, particularly where resistance to light or enzymatic breakdown gives an edge over standard aromatic systems. The 6-fluoro substitution translates directly to improved field stability; we’ve heard from several clients that batches made from our acid outlasted competitor-derived analogs in field stability trials by over 20 percent. As a manufacturer, getting this kind of feedback tells us not only that the synthetic route is robust, but that our attention to thermal and photochemical stability during drying and packing isn’t just academic—it matters out on the farm or in the greenhouse, too.
Real production doesn’t operate in the world of theory or catalogues. Over the years, we’ve faced—and solved—practical problems that absolutely affect users on the bench and in manufacturing. Early synthetic routes led to issues with over-fluorination, where traces of difluoro or even trifluorochromene crept in at levels that could only be spotted by high-res mass spectrometry. This didn’t show in HPLC purity, but for clients making regulatory filings, even these low ppm impurities led to failed documentation. We revised reagent ratios, adopted inline FTIR monitoring, and switched to purer precursors, cutting these impurities below detectable limits. Stability in storage also created lessons; the free acid can decarboxylate if exposed to heat or moisture, so we moved to cold-room storage and ship with desiccant-packed bottles as the industry norm, not an upcharge.
Scalability remains a hot topic among procurement teams looking to bridge R&D and pilot plant scales without changing supplier due to batch limitation. Our reactors are engineered for linear scaleup from 1-kg to 100-kg runs, thanks to years of tracking exotherm profiles and solvent composition at each step. This hands-on learning makes a clear contrast to generic intermediates sourced through brokers relying on small-scale lots from varied sources. We’ve learned, sometimes the hard way, that good mixing and temperature control beat fancy new catalyst systems, and staying responsive to changes in solvent availability or pricing keeps the process robust no matter what the supply chain throws our way.
The world of chromene synthesis offers up plenty of analogs: unsubstituted chromene-2-carboxylic acid, chloro derivatives, and more highly fluorinated species are all part of the API starting material parade. We’ve tracked user feedback across hundreds of pilot schemes. The 6-fluoro version occupies a unique niche. Unsubstituted chromene acids, while easy to make and low cost, lack the metabolic durability that pharma clients build into modern patent filings or require for overcoming stability hurdles in lead optimization. Chlorinated chromenes can be more reactive but often show reduced solubility and can trigger complications with byproduct formation or environmental handling.
Heavily fluorinated analogs, like difluoro or trifluoro derivatives, attract attention due to extreme electron withdrawal, but in our hands those compounds see less uptake in customer applications. They often suffer from reduced reactivity during downstream functionalization. Our acid, with a single carefully positioned fluorine, tunes the balance between resistance to metabolic oxidation (important for both pharma and agchem work) and compatibility with common coupling reactions. Customers explain that this hits the "sweet spot": advanced enough for stability, but not so over-modified as to wreck established transformations.
On the technical handling side, particle morphology and moisture response differentiate our product from those made in more humid or uncontrolled sites. We’ve heard too many stories of buyers receiving caked, non-flowing solid from cross-continental resellers, which chokes dispensing systems and increases rework. We control humidity at every packing stage, and include moisture indicators as part of each shipment to validate integrity upon arrival. These steps cut the risk of hidden clumping, a common problem with carboxylic acids processed without true climate control.
Direct users face sharp questions from their own EH&S teams and auditors about traceability, batch consistency, and documentation trails. Because we operate as not just a bulk producer but a long-term supplier to regulated industries, our documentation chain and safety files draw directly from on-site manufacturing records. Every certificate matches physical retain samples, and our labeling includes not just lot number, but full synthesis date and processing history. Clients prepping for audits appreciate this clarity, as do our own local regulatory inspectors.
Material handling safety shapes every step of our workflow. We supply user data on dust control, spill response, and personal protective requirements that draw from incident logs and in-lab drills—not just pulled from published MSDS lists. If a process team wants to know typical exotherm temperatures or solvent vapor evolution, we supply findings from both scheduled and unscheduled production runs. This hands-on support means fewer surprises when launching pilot batches or transitioning to full-scale manufacturing.
For those with strict compliance targets, knowing the fluorine source and tracking contaminants like PFAS forms key parts of the risk assessment. Our plant takes this seriously, patterning fluorine procurement and acid quenching protocols after the latest environmental guidelines. Customers benefit from this by having actionable, transparent data on every bottle — an expectation in new-molecule filings from pharma and agchem companies worldwide.
In a marketplace crowded with catalog resellers and offshore brokers, in-house synthesis delivers hard advantages. We build new process modifications into the workflow as feedback rolls in—sometimes prompted by users facing new conditions or putting the acid to use in systems we could never have predicted. This closed loop between user and manufacturer enables tweaks to aspects like residual solvent threshold or alternate salt forms far faster than would be possible through an importer or repackager. For ongoing projects, clients often need a few kilos at first, then suddenly ramp to hundreds—all without shifting sourcing strategy. Owning both the chemistry and the logistics lets us perform this pivot.
Sometimes, the most important feedback comes not from a lab director but from a technician on an assembly line noticing smoother dissolution or faster filtration. We welcome these insights and have, more than once, changed handling and storage protocol based on field notes from experienced users. This doesn’t turn up in published papers, but it sharply differentiates a product built for daily use rather than one moved by the container load through anonymous channels.
We see future potential for 6-fluoro-3,4-dihydro-2H-chromene-2-carboxylic acid in developing areas such as advanced materials, where tailored aromatic acids are being explored for photoresist formulations and specialty coatings. Its unique reactivity profile—unmatched by either simple acids or heavily fluorinated analogs—gives opportunities in areas where thermal and chemical stability, fine-tuned by-position fluorine substitution, and clean conjugation routes matter. Our R&D pipeline keeps one eye on these trends, directing pilot batches toward customers with whom we can collaborate on use-case optimization.
On plant floors, we continue to invest in process robustness—focused on modular reactor systems, inline real-time analytics, and greener quench protocols that not only reduce environmental footprint but cut operating costs for everyone involved. We have learned over many years that customer needs evolve; maintaining an agile, factory-based production pipeline lets us keep pace and deliver the tweaks and upgrades that can only come from producer-level expertise. As direct feedback from users comes in—be it new downstream chemistry or evolving regulations—we adapt, drawing from the bench and the line.
6-fluoro-3,4-dihydro-2H-chromene-2-carboxylic acid stands as more than just another intermediate on a product list. Built from the ground up with a focus on real-world use, our product draws on daily lessons from synthesis and application alike. This compound’s unique blend of electronic tuning, stability, and flexibility only shines during hands-on work—ported directly from our reactors to your lab or production facility. That difference, proven by years of direct feedback, is what keeps us committed to driving performance and reliability in every shipment.