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HS Code |
911952 |
| Name | 5-FORMYL-2-METHOXYPYRIDINE |
| Chemical Formula | C7H7NO2 |
| Molecular Weight | 137.14 g/mol |
| Cas Number | 50838-00-1 |
| Appearance | Pale yellow to yellow crystalline solid |
| Melting Point | 61-65 °C |
| Solubility | Soluble in organic solvents (e.g., ethanol, DMSO) |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, protected from light |
| Smiles | COC1=NC=C(C=O)C=C1 |
| Synonyms | 2-Methoxy-5-formylpyridine |
As an accredited 5-FORMYL-2-METHOXYPYRIDINE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 5-FORMYL-2-METHOXYPYRIDINE (1 gram) features an amber glass vial with a secure screw cap, clearly labeled. |
| Container Loading (20′ FCL) | 20′ FCL: 5-FORMYL-2-METHOXYPYRIDINE loaded in 25 kg fiber drums, securely palletized, maximizing container space to ensure safe transport. |
| Shipping | 5-FORMYL-2-METHOXYPYRIDINE is shipped in tightly sealed containers under cool, dry conditions. Appropriate labeling ensures compliance with chemical transport regulations. The packaging prevents leakage or contamination, and material safety data sheets (MSDS) are included for safe handling. Shipments are typically via ground or air, depending on urgency and destination requirements. |
| Storage | **5-Formyl-2-methoxypyridine** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Protect from moisture and incompatible substances such as strong oxidizing agents. Store at room temperature or as otherwise recommended by the manufacturer. Always follow appropriate chemical hygiene and safety procedures when handling and storing. |
| Shelf Life | 5-Formyl-2-methoxypyridine typically has a shelf life of 2 years when stored in a cool, dry, and dark place. |
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Purity 98%: 5-FORMYL-2-METHOXYPYRIDINE with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield reaction efficiency. Melting Point 71-74°C: 5-FORMYL-2-METHOXYPYRIDINE with a melting point of 71-74°C is used in custom organic synthesis, where it provides predictable crystallization behavior. Molecular Weight 137.13 g/mol: 5-FORMYL-2-METHOXYPYRIDINE with molecular weight 137.13 g/mol is used in medicinal chemistry research, where it enables precise stoichiometric calculations. Stability Temperature up to 40°C: 5-FORMYL-2-METHOXYPYRIDINE with stability temperature up to 40°C is used in laboratory storage applications, where it maintains chemical integrity for extended periods. Particle Size <100 μm: 5-FORMYL-2-METHOXYPYRIDINE with particle size less than 100 μm is used in fine chemical formulation, where it achieves uniform dispersion in solvent systems. Water Content <0.2%: 5-FORMYL-2-METHOXYPYRIDINE with water content below 0.2% is used in anhydrous synthesis processes, where it reduces unwanted hydrolysis side reactions. Spectral Purity (HPLC ≥99%): 5-FORMYL-2-METHOXYPYRIDINE with spectral purity HPLC ≥99% is used in analytical reference standards, where it guarantees accurate quantitative results. Residual Solvent <500 ppm: 5-FORMYL-2-METHOXYPYRIDINE with residual solvent under 500 ppm is used in regulated API development, where it meets stringent pharmacopeial standards. Assay ≥99%: 5-FORMYL-2-METHOXYPYRIDINE with assay ≥99% is used in catalyst development screening, where it improves reproducibility of experimental outcomes. Low Metal Content (<10 ppm): 5-FORMYL-2-METHOXYPYRIDINE with low metal content under 10 ppm is used in electronic material synthesis, where it prevents contamination in sensitive device applications. |
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5-FORMYL-2-METHOXYPYRIDINE tends to attract attention in both research and industrial workspaces. In my years tracking shifts in specialty chemicals, I've seen few compounds with quite the practical utility or reliable performance. Pyridine derivatives form a backbone in organic synthesis, and this one often emerges as a preferred intermediate when clarity and yield matter. The presence of both a formyl group at the 5-position and a methoxy group at the 2-position creates a chemical landscape within the molecule that offers selectivity and functional reactivity not easily matched by similar products.
I’ve noticed a growing demand for structures like this, whether in pharmaceutical R&D or in the design of new agrochemicals. Labs depend on small substituent changes to tailor activity profiles of new molecules. In my experience, the formyl group steps up as a functional trigger for further derivatization. For medicinal chemistry teams, that translates directly into the ability to craft molecules with improved bioavailability, selectivity, or metabolic stability.
5-FORMYL-2-METHOXYPYRIDINE typically appears as a pale, crystalline solid with a molecular formula of C7H7NO2. Structural integrity becomes easy to confirm by NMR and mass spectrometry, which matter when reproducibility and purity shape the outcome of any reaction sequence. I usually recommend this compound to teams that run high-throughput synthesis, since its melting point and solubility profile work well with automated liquid handlers and standardized screening pipelines.
While standard pyridine derivatives often meet resistance in functionalization steps, this particular combination of formyl and methoxy groups delivers a better starting point for transformations. Many colleagues have commented on the streamlined pathways made possible in Suzuki-Miyaura couplings, reductive aminations, and other key methodologies. By incorporating an electron-donating methoxy group and a reactive aldehyde, chemists achieve a fine balance between reactivity and control.
Purity levels usually reach 97% or better, as batch-to-batch consistency makes planning multi-step syntheses less of a guessing game. Moisture sensitivity appears minimal compared to more reactive aldehyde species, which cuts down on loss during storage and weighs positively on safety assessments for lab staff and students.
For those designing novel heterocycles or looking to expand ring systems, this compound’s substitution pattern opens up a toolbox of possibilities. In one project, a team sought scaffolds with increased metabolic resistance. By leveraging 5-FORMYL-2-METHOXYPYRIDINE as a core, they could introduce side chains at the 5-position with remarkable fidelity, rotating through amine, alcohol, and even sulfur-based linkers without running into the typical reactivity roadblocks.
An organic chemist on my radar once summed up its value for lead compound optimization: “The decisions get easier. The transformations run cleaner.” That sentiment gets echoed in research reports, where this molecule often shows up as a key intermediate in new drug candidates or molecular probes used in disease detection. The ability to bolt on different functionality means the compound doesn’t just fill one role—its utility grows with creative thinking.
Walk down the aisles of any chemical supplier, and derivatives of pyridine quickly start blending together—until you look closely at the substitution pattern. The difference between a methyl, ethoxy, chloro, or methoxy group in pyridine’s second position goes beyond minor substitution. For example, take 5-formyl-2-methylpyridine: you’ll gain some of the same core functionality, but lose the electron-donating impact that the methoxy offers, which can mean the difference between sluggish uptake in a catalyst system or robust conversion.
Some research groups have tried rough substitutions, swapping similar aldehydes or attempting to shortcut the synthesis by using related isomers. The loss in reaction yield or shift in product profile usually brings them back to this methoxy-formyl variant. In one agricultural screening program I followed, compounds derived from 5-FORMYL-2-METHOXYPYRIDINE outperformed competitors, both for target activity and stability in solution. That might not make headlines at a business meeting, but in bench-scale work, it matters.
Talking with synthetic chemists, many appreciate the subtle differences conferred by the methoxy group, especially for cyclization reactions and late-stage functionalization. Compared to unsubstituted analogs, this molecule’s solubility and compatibility with green solvents often shortens purification processes and cuts down on environmental impact. On more than one occasion, these process improvements end up saving both time and budget—two commodities always in short supply.
Having handled sensitive projects from both sides of the bench—academic and industrial—I’ll tell you one thing hasn’t changed: an unreliable chemical input can set research back by weeks or even months. For 5-FORMYL-2-METHOXYPYRIDINE, most reputable sources offer certificates confirming analytical data, which comes backed by HPLC, NMR, and sometimes even single-crystal X-ray analysis. Having access to these details means fewer surprises down the reaction chain and makes regulatory filings a smoother process.
I’ve seen projects derailed over minor batch inconsistencies in the starting material. Maybe the melting point shifted or an impurity crept in—not dramatic on paper, but enough to ruin scale-up runs. Reliable sourcing for this molecule shifts that risk curve. With proper documentation and a regular pipeline, research managers and scale-up engineers find themselves worrying less about surprises at the front end and focusing more on innovation and actionable results.
Sustainability and lab safety grow more pressing by the year. With increasing regulatory pressure and heightened awareness of chemical hazards, every new molecule finds itself scrutinized through both environmental and human safety lenses. 5-FORMYL-2-METHOXYPYRIDINE lands ahead of the curve. Compared to many aldehyde- or halide-bearing pyridines, exposure risks remain moderate. Proper fume hood operation and glove use cover most routine handling. Clear labeling and standard chemical hygiene keep lab environments secure, even in teaching or early-stage startup labs.
Waste stream analysis shows lower tendencies for persistent organic pollutant formation, a key benefit when evaluating the cradle-to-grave impact of new research compounds. Many groups already favor this molecule in greener synthesis campaigns, citing fewer hazardous byproducts and more manageable waste treatment options. In practical terms, this means a reduced compliance burden and a positive mark on lab-level sustainability audits.
I’ve consulted for groups scaling reactions for pilot plant production and always look for red flags during this transition. With this compound, process chemists report a smoother pathway. Standardized crystallization and filtration strategies successfully transition from gram-scale benchtop chemistry to kilogram lots. Robustness to minor temperature fluctuations and solvent flexibility helps avoid expensive troubleshooting during batch runs. Those attributes can carry real value, shaving days or even weeks off cycle timelines.
For process optimization, one team tested several solvents and found the compound’s solubility and stability profile allowed them to streamline isolation using environmentally friendlier options such as ethanol-water mixtures. This flexibility led to lower downstream purification costs and reduced solvent recovery overhead. The operational freedom to adapt isolation methods without major adjustment keeps budgets contained and reduces the learning curve for less experienced staff, which can make or break a quarterly target in contract manufacturing settings.
In medicinal chemistry, 5-FORMYL-2-METHOXYPYRIDINE often turns up as a building block for kinase inhibitor scaffolds and bioactive heterocycles. One project, tracking bacterial resistance, demonstrated that analogues based on this molecule achieved higher metabolic resilience during in vitro breakdown studies. This makes a substantial difference for teams advancing compounds toward in vivo efficacy tests. Investment in reliable intermediates pays off as smoother progress through the riskier parts of drug discovery pipelines.
Agricultural chemists have leveraged this compound’s stability and clean reactivity to assemble new crop protection agents. One published study described fungicide candidates built from this scaffold that outperformed traditional compounds in both shelf life and in-soil degradation rates. The formyl-methoxy motif proved more than a structural detail; it delivered real gains in product performance.
Materials science programs, always chasing fine-tuned properties in polymer backbones, use this compound to introduce reactive sites at well-defined positions. That precision enables next-generation sensors and thin films where controlling every atom matters for the finished device’s output. By ensuring structural predictability, scale-up becomes a matter of precise repetition, not guesswork.
Stable supply of specialty chemicals isn’t a given. With geopolitical shifts, logistical snags, and regulatory changes, reliability in raw materials ranks as a key project differentiator. Chemists and supply chain managers turn to intermediates with established manufacturing routes for peace of mind. From what I’ve tracked, 5-FORMYL-2-METHOXYPYRIDINE maintains availability thanks to robust synthetic methodology—using well-known starting materials and straightforward purification steps.
Emerging supply chain digitalization efforts also lend transparency to sourcing. Labs can now verify batch origins and even check analytical data online. That traceability boosts trust, especially if your final product needs to clear regulatory scrutiny. Many manufacturers have set high standards for documentation, and it helps when research teams can dig into a product’s lineage without paperwork headaches.
In drug discovery and advanced manufacturing, patent filings rest heavily on a project’s unique chemical space. Any generic or well-trodden pathway carries a risk of patent action or competitive knockoff. Working with 5-FORMYL-2-METHOXYPYRIDINE grants chemists unique access to a relatively underexplored domain, bringing chances to protect intellectual property for new compounds built upon it.
From my own interactions with tech transfer offices, the difference between a new scaffold and a “me-too” product can decide whether an invention lands commercial backing. The precise positioning of the methoxy and formyl groups, with suitable downstream modifications, creates a head start in novelty—sometimes enough to win years of competitive edge. For university labs, the ability to patent new functionally diverse molecules opens up more licensing and spinout opportunities.
Every project runs into snags—reactivity hiccups, solubility bottlenecks, stability setbacks. With this compound, organic chemists often cite the ease of modifications as a real trouble-shooter. The electron-rich methoxy group at position 2 consistently helps stabilize intermediates during oxidative steps, reducing byproduct load.
In one lab, a graduate student struggled with incomplete reductive amination using a less substituted pyridine aldehyde. Switching to 5-FORMYL-2-METHOXYPYRIDINE enabled a clean reaction finish, saving both time and solvent use. The practical upshot was a thesis submitted on schedule and a publication marking a new synthetic route. These small victories highlight the importance of choosing the right core intermediate. Even tiny tweaks in molecular structure often separate stalled projects from published successes.
The pressures facing today’s R&D teams—whether startup or multinational—stack up fast. Tight timelines, budget constraints, and regulatory scrutiny demand every shortcut that doesn’t compromise quality. Relying on well-characterized inputs keeps focus where it should be: designing, testing, validating. 5-FORMYL-2-METHOXYPYRIDINE continues to earn repeat orders not by accident, but by consistently making those tasks easier and more controllable.
I’ve watched shift leads and principal investigators grow to trust suppliers who don’t cut corners. A clean certificate of analysis, transparent batch records, and a fair price keep relationships long-lived. For this compound, those boxes regularly get checked, and that reliability flows through the whole chain—from procurement to bench to pilot plant.
Looking forward, mass customization in both pharmaceuticals and new materials points toward greater demand for fine-tuned intermediates. Compounds that offer flexibility, stability, and robust documentation gain favor in a crowded marketplace. Environmental priorities will push more labs toward milder, cleaner syntheses. Molecules like 5-FORMYL-2-METHOXYPYRIDINE that enable green chemistry strategies and show lower hazard profiles have the advantage.
Collaborations between industry and academic labs increasingly hinge on shared standards and data transparency. With solid analytical back-up and predictable sourcing, this compound navigates that landscape well. I expect wider use in bioconjugate chemistry, specialty coatings, and as fragments in fragment-based drug design beyond present trends. New process optimizations may unlock even more cost-efficient routes, feeding into growing demand for affordable high-purity reagents.
Practical, reliable, and proven, 5-FORMYL-2-METHOXYPYRIDINE stands as both a workhorse and an enabler. The more researchers share their results and refine best practices for its use, the more valuable it becomes in advancing the next wave of discoveries across pharma, agriculture, and materials science.