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HS Code |
318666 |
| Productname | 5-(2-Chlorophenyl)-2-Furoic Acid |
| Casnumber | 82356-51-2 |
| Molecularformula | C11H7ClO3 |
| Molecularweight | 222.63 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 146-150°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically >98% |
| Smiles | C1=CC=C(C(=C1)C2=CC=C(O2)C(=O)O)Cl |
| Inchi | InChI=1S/C11H7ClO3/c12-8-3-1-2-6-9(8)10-4-5-15-11(10)7(13)14/h1-6H,(H,13,14) |
| Storageconditions | Store at room temperature, away from moisture and light |
As an accredited 5-(2-Chlorophenyl)-2-Furoic 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 5-(2-Chlorophenyl)-2-Furoic Acid, securely sealed, labeled with chemical details and hazard information. |
| Shipping | 5-(2-Chlorophenyl)-2-Furoic Acid is shipped in tightly sealed containers under cool, dry conditions, compliant with chemical handling regulations. Packages are clearly labeled with hazard information. The chemical is transported in accordance with international and local guidelines to ensure safety and prevent contamination, damage, or exposure during transit. |
| Storage | Store **5-(2-Chlorophenyl)-2-Furoic Acid** in a tightly sealed container, away from direct sunlight, ignition sources, and moisture. Keep in a cool, dry, and well-ventilated area, ideally at room temperature. Avoid contact with strong oxidizing agents. Clearly label the container, and handle with appropriate personal protective equipment to prevent inhalation, ingestion, or skin contact. |
Applications of 5-(2-Chlorophenyl)-2-Furoic Acid in Industrial Manufacturing5-(2-Chlorophenyl)-2-Furoic Acid is a specialty intermediate produced in our facility and supplied to industrial clients worldwide. We deliver tight specification control to meet critical downstream requirements. Below, we outline several core application fields with detailed process insights. 1. Pharmaceutical Intermediates for Anti-inflammatory Drug SynthesisThis compound functions as a key building block for the synthesis of several non-steroidal anti-inflammatory drug APIs, notably in furan-based molecule scaffolds. Major pharmaceutical manufacturers use it at the condensation step with amine substrates for further cyclization. We supply bulk volumes with stringent impurity profiling for regulatory submission batches. Expert teams collaborate with formulation specialists to control reaction purities and meet validated manufacturing protocols across global facilities. Industry compliance standards
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2. Agrochemical Active Ingredient PrecursorChemical crop protection producers utilize 5-(2-Chlorophenyl)-2-Furoic Acid as a controlled intermediate for selective herbicide and fungicide synthesis. Our supply supports heterocyclic coupling and ring-modification reactions for downstream active ingredient (AI) processes. Manufacturers invest in automated dosage and in-line monitoring to align reaction yield with seasonal production schedules. Industry compliance standards
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3. Specialty Polymer Additive SynthesisAdvanced materials manufacturers incorporate this acid as a functional modifier in specialty polymers. End users employ it to achieve targeted hydrophobicity and chemical resistance in engineering plastics and coatings. Our product consistently meets color, acidity, and trace impurity targets critical for reproducible polymerization. We offer logistical solutions for bulk supply to continuous production plants in the plastics sector. Industry compliance standards
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4. Fine Chemical Intermediate for Dye and Pigment ManufacturingDye industry clients rely on this raw material for the synthesis of complex heterocyclic pigments. It supports colorant development via Knoevenagel condensations or as an acylating agent in phase-transfer catalysis. Quality control includes full-spectrum analysis and batch-to-batch color index certification. Long-term partners have access to tailored lot sizes and supply chain visibility for regulated sectors. Industry compliance standards
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As a chemical manufacturer, we spend years listening to customers and fine-tuning production lines for each specialty chemical. The compound 5-(2-Chlorophenyl)-2-Furoic Acid is a firm example. Its structure brings together a furan ring, a carboxylic acid, and a 2-chlorophenyl group, introducing a precise balance of reactivity and stability. Our daily work keeps us embedded in the actual synthesis challenges chemists face, not just generic claims. We produce this molecule for researchers and producers working at the front line of pharmaceutical intermediates, agrochemicals, and specialty materials development.
We know that reproducibility keeps a synthesis on track. Over batches and years, uncontrolled variation breaks processes and destroys trust. Our team controls incoming raw materials through robust supplier qualification, then maintains strict process parameters throughout every run: temperature, pH, solvent composition, and purification stages all follow procedures refined with feedback from synthetic chemists. Chemists will notice that our 5-(2-Chlorophenyl)-2-Furoic Acid typically arrives as a white to light tan crystalline powder, its purity supported by routine HPLC analysis and identity confirmation by NMR and MS.
This isn’t just about hitting a COA spec. Any material that leaves our facility has crossed five separate QC checks, each with criteria set by our own R&D chemists and confirmed by process engineers. Material that comes off color or with trace byproducts never ships out, because we know firsthand what a downstream purification headache means in a long synthetic route. We’re not shielded lab managers; we’ve been the ones cleaning up after a poor-quality input.
5-(2-Chlorophenyl)-2-Furoic Acid doesn’t look flashy on paper, but the specifics of its structure mean it behaves in ways that matter in the lab. The furan ring carries electron richness, allowing for coupling strategies rarely open to benzene alone, while the 2-chlorophenyl group introduces a handle for palladium-catalyzed transformations. We’ve seen our partners use it to build up diverse libraries of heterocycles or as a stepping stone into more functionalized derivatives. The carboxylic acid makes derivatization straightforward and opens the door for amide or ester formation.
In our experience, labs working on multi-step pharmaceutical syntheses often reach for this compound when other substituted aromatic acids don’t give them enough flexibility. Synthetic routes that stall with standard benzoic acids or fail to activate under mild conditions often find success here. Direct comparison in micro-scale trials show better yields in Suzuki and Heck couplings, and the furan moiety introduces unique reactivity that expands downstream options.
We’ve built close partnerships with pharmaceutical development teams, specialty polymer researchers, and even material scientists developing new surface treatments. Most interest in 5-(2-Chlorophenyl)-2-Furoic Acid still comes from the pharmaceutical sector, especially those working on small molecule APIs or structural analog design. The molecule’s dual ring system—with furan and chlorophenyl—lends itself to modifications in the search for new biological activity. Recent inquiries from university research groups looked to this compound as a scaffold for kinase inhibitors and for neurochemical modulator projects.
Agrochemical innovators have approached us looking for reliable stocks. In this field, the acid group opens up additional conjugation options, where binding to different functional moieties tailors the compound for crop protection or growth regulation. We support those customers with batch documentation and adaptability, scaling up to match their needs as projects reach pilot plant scale.
For material science teams, the electron-rich furan and the carboxylic acid function as unique points for building polymers with specific optoelectronic properties. The chlorinated aromatic ring brings opportunities for controlled substitution and post-polymerization modifications that standard benzoic acids just do not.
Among specialists, purity and consistency decide whether a compound speeds up research or causes expensive troubleshooting. It’s not unusual for us to run 99% HPLC-purity batches, while intentionally offering lower purity material for pilot feasibility studies where budgets run tight, and non-critical runs can settle for less rigorous material.
Every customer asks about melting point range, moisture content, and impurity profiles. Instead of hiding behind standard paperwork, we share batch data and previous stability studies. Analytical packages usually include 1H and 13C NMR, mass spectrometry, HPLC chromatograms, and, on request, elemental analysis. Our own plant runs cross-validation against external labs regularly, so no one is working on assumptions.
Researchers need more than just “looks white” quality control. We’ve run panel studies where side-by-side uses in Suzuki reactions showed our batches consistently outperforming competitors in conversion rate and byproduct control—data regularly shared with partners.
Laboratory and production staff alike comment on the frustration of sticky powders, poorly sealed bags, or oddly chosen vessels for shipping. Our batches ship in double-walled polyethylene containers or amber glass bottles depending on hazard and sensitivity requirements. During our pilot scaling phase, the R&D teams worked directly with our packaging crew, finding container types that avoid static, minimize sticking, and keep transfer loss to a minimum. The result is product that pours easily at the bench or into reactors, whether you’re drawing out 25 grams or 5 kilos.
Each lot’s stability under ambient, refrigerated, or inert conditions is an important focus of our process improvement. Current stability data cover over 18 months at ambient and 30 months refrigerated, with no measurable drop in purity or color shift. These are not marketing numbers, but collected from lots held at company and partner labs over years. We don’t sell “expired” material under new labels; our customers know they order with confidence.
We aren’t in the business of mass-market catalogs, where high volume and low traceability sometimes open the door for cross-contamination or batch co-mingling. Our segmented reactor lines and glove box isolation steps allow us to keep furoic acids away from halogenated pyridines and related families, so the customer’s analytical screens don’t pick up surprise unknowns.
We’ve fielded calls from purchasing and technical teams at pharmaceutical plants who suffered from mystery impurities in key intermediates, only to trace the cause back to poorly controlled secondary reactions at third-party toll manufacturers. As our methods rely on single-use filtration modules and individual drying protocols, we isolate and contain each lots, logging every batch against a chain of internal records.
Feedback loops drive our improvement. A process manager at a generic drug manufacturer once spotted a trace byproduct in a small shipment, shared his analytical notes, and within a month, our team resolved the root cause and improved the purification stage. Every improvement we make around 5-(2-Chlorophenyl)-2-Furoic Acid filters out headaches for chemists, speeding up their project milestones and freeing QC to focus on the actual experimental outcomes.
This compound doesn’t just stand apart from lower-spec acids; it stands apart from more standard aromatic or phenyl-furan analogs. In parallel runs we have observed time savings during coupling reactions relative to materials with broader impurity windows. Chemists’ feedback frequently reports less time spent resolving ambiguous spots on TLC and cleaner crystallization, leading to easier filtration and higher final yields. That alone cuts several hours from a week spent in pilot synthesis. Our commitment to purity is not just about paperwork; it turns up as cleaner NMRs, better chromatographic performance, and easier scalability.
The furan’s electron-rich character makes the acid more reactive for carboxylate activation, and the chlorophenyl's habit of sitting on the ortho position changes the compound’s reactivity profile enough to open new options for ring-closing or substitution. This isn’t always the case with other commercial sources, where mixed isomers and spectroscopically heterogeneous material can cloud interpretation or cause false negatives in structure-activity relationship studies.
A lot of resellers offer generic catalog numbers, drop a MSDS, and point to a COA. Our team gets involved from project start: reviewing routes, talking synthesis through with chemists, and suggesting modifications to save material or improve step economy. Some long-term partners have looped us in on pilot plant runs to help troubleshoot scale-dependent challenges—solvent swaps, temperature cycling, and in-line analytical setups.
No single synthetic plan is “one size fits all,” so our flexibility in accommodating custom lots, modified purification, or just-in-time delivery arises from real production experience. Sometimes a customer working under strict timelines needs their lot with less than half the typical lead time. Our plant operators pull shifts, and chemists oversee every batch with live data tracking, to prioritize those orders. This is the difference actual manufacturing makes.
We field technical questions directly, not through layers of sales assistants. Customers have direct access to the chemists and engineers who run these reactors and design the processes. Conversations steer toward practical troubleshooting, such as minimizing hydrolysis risk in storage or advice for in-lab handling, rather than relying on boilerplate care instructions.
Our work doesn’t stop after shipment. We collect user feedback. Recently, a customer noted issues with particle size and flow in automated feeders. We responded by modifying our final crystallization conditions to produce more uniform particle shape and improve bulk density, results reflected in the latest lots. This attention to the production chain—from clarification to drying and sieving—amplifies lab efficiency and scale-up stability.
Every batch of 5-(2-Chlorophenyl)-2-Furoic Acid creates an opportunity to refine and enhance output for a more seamless user experience. Troubleshooting never ends, and we treat every customer problem as an opportunity to look for process innovations.
As regulatory standards for chemical use in pharmaceutical and agricultural spaces grow more complex, we keep up with updated documentation and traceability measures. Our team maintains internal and third-party data packages for key compliance needs. Whether a customer is preparing a DMF, regulatory filing, or submission to international oversight, we facilitate due diligence checks and respond to auditing requirements. We’ve seen firsthand where missing documentation can derail a project or introduce unexpected costs, so we maintain a conservative approach that anticipates changes in the compliance landscape.
Our facilities have moved toward greener, safer synthesis routes—including solvent replacement and waste minimization—without sacrificing the reliability of our core product. That helps customers make easier environmental declarations downstream, and fulfills our responsibility as a manufacturer to minimize footprint and workplace hazard. Safety data and storage recommendations come grounded in real operational risk management, not generic cut-and-paste statements.
The real value in sourcing 5-(2-Chlorophenyl)-2-Furoic Acid from a dedicated manufacturer comes down to trust and technical collaboration. Our chemists don’t wait for customer complaints; they look plainly at how each lot is being used in end applications and proactively offer support. We share details of our synthetic routes and analytical protocols with users upon request, so they can make informed decisions and streamline their own process development.
We keep communication candid. Data showing environmental, health, or process risks aren’t hidden; they turn into open discussions so the user can adapt safety protocols or process setups. Beyond shipping a drum or sending a certificate, we step into real project milestones and support each experiment or process scale-up.
By manufacturing, analyzing, and supporting the use of 5-(2-Chlorophenyl)-2-Furoic Acid directly, we help research teams, pilot plants, and full-scale production facilities meet the tough challenges of advanced molecule synthesis. Over time, these experiences shape the way we produce, test, and deliver this and every other specialty compound in our line.
The chemical needs of research and industry change quickly. New reactions surface. Regulatory expectations grow tougher. Customer timelines grow shorter and budgets tighter. By rooting every batch of 5-(2-Chlorophenyl)-2-Furoic Acid in direct technical experience and a willingness to engage, we keep providing the reliability, flexibility, and quality that ambitious customers need. Our approach doesn’t just rest on what works today, but on always preparing for the next synthetic challenge—one hard-earned batch at a time.