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HS Code |
533687 |
| Chemical Name | 2-Methylsulfanyl-oxazolo[5,4-b]pyridine |
| Molecular Formula | C7H6N2OS |
| Molecular Weight | 166.20 |
| Cas Number | 868273-23-4 |
| Appearance | White to off-white solid |
| Melting Point | 121-124°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically >=98% |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Smiles | CSC1=NC2=CN=CC=C2O1 |
| Inchi | InChI=1S/C7H6N2OS/c1-11-7-8-6-5(9-7)3-2-4-10-6/h2-4H,1H3 |
| Synonyms | 2-(Methylthio)oxazolo[5,4-b]pyridine |
| Applications | Pharmaceutical intermediate, chemical research |
As an accredited 2-Methylsulfanyl-oxazolo[5,4-b]pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle containing 10 grams of 2-Methylsulfanyl-oxazolo[5,4-b]pyridine, labeled with hazard warnings and batch information. |
| Container Loading (20′ FCL) | 20′ FCL container loaded with securely packed drums of 2-Methylsulfanyl-oxazolo[5,4-b]pyridine, with proper labeling and moisture protection. |
| Shipping | 2-Methylsulfanyl-oxazolo[5,4-b]pyridine is shipped in a tightly sealed, chemical-resistant container to prevent moisture and contamination. It is transported under standard conditions, away from incompatible substances, and accompanied by the appropriate safety data sheets in accordance with all regulatory requirements for chemical handling and transport. |
| Storage | Store **2-Methylsulfanyl-oxazolo[5,4-b]pyridine** in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from light and moisture. Label container clearly and keep away from sources of ignition. Follow all relevant safety regulations for handling aromatic heterocycles and sulfur-containing compounds. |
| Shelf Life | 2-Methylsulfanyl-oxazolo[5,4-b]pyridine typically has a shelf life of 2 years when stored in a cool, dry place. |
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Purity 98%: 2-Methylsulfanyl-oxazolo[5,4-b]pyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction specificity and minimized by-product formation. Melting Point 142°C: 2-Methylsulfanyl-oxazolo[5,4-b]pyridine with a melting point of 142°C is used in high-temperature organic syntheses, where it provides thermal stability during processing. Molecular Weight 182.24 g/mol: 2-Methylsulfanyl-oxazolo[5,4-b]pyridine at 182.24 g/mol is applied in drug design studies, where its defined molecular mass supports accurate compound formulation. Solubility in DMSO: 2-Methylsulfanyl-oxazolo[5,4-b]pyridine soluble in DMSO is used in cellular assay development, where it enables reliable compound delivery to biological systems. Particle Size <10 μm: 2-Methylsulfanyl-oxazolo[5,4-b]pyridine with a particle size below 10 μm is employed in solid dosage formulation, where it enhances uniform dispersion and dissolution rates. Stability at 25°C: 2-Methylsulfanyl-oxazolo[5,4-b]pyridine demonstrating stability at 25°C is used for long-term storage in chemical libraries, where it maintains compound integrity. LogP 2.3: 2-Methylsulfanyl-oxazolo[5,4-b]pyridine with logP 2.3 is utilized in medicinal chemistry studies, where its lipophilicity improves membrane permeability profiling. |
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In the chemical manufacturing industry, efficiency and purity drive every decision that takes a compound from the reactor to the end-user’s application. Handling 2-Methylsulfanyl-oxazolo[5,4-b]pyridine over the years has taught us that consistency in the synthesis process pays back at every step, right from lab-scale optimization to routine production batches. This material features a unique pyridine core with a methylsulfanyl group, which opens doors for several industries—predominantly pharmaceutical research, crop protection, and materials development.
Exacting standards matter when two similar pyridonederivatives enter the same lab. In many reactions, minor differences in substitution lead to significantly different outcomes. We learned early on that controlling the methylsulfanyl group's placement is not only a synthetic challenge but a factor that influences reactivity, solubility, and compatibility with other building blocks. This isn’t chemistry for chemistry’s sake: model variation at this stage determines what’s possible in downstream transformations, particularly where substitution patterns impact pharmacological screening or material properties.
Our focus in manufacturing 2-Methylsulfanyl-oxazolo[5,4-b]pyridine has always turned to purity and batch-to-batch reproducibility. Solvents, starting materials, and purification approaches each contribute to the product’s final profile. Typical lots have minimal sulfur-related impurities since these often cause headaches in scale-up or bioactive compound synthesis. Years of internal analysis show that residual metals and halogenated byproducts lurk at parts-per-million levels, so we invest in scrupulous purification and use high-grade precursors.
Physical properties like melting point hint at purity but aren’t always the whole story. Our analytics include NMR, HPLC, and mass spectrometry for every batch, with particular care to confirm the identity of the methylsulfanyl substituted ring. Moisture content creates problems in coupling reactions, so we regularly monitor Karl Fischer values and limit storage times for bulk material whenever possible. For some partners, knowing the particle size and specific surface area adds value, especially for formulation or subsequent reaction kinetics.
Chemists in R&D often approach us looking to create new libraries of heterocyclic compounds. The oxazolopyridine structure, combined with the methylsulfanyl group, lends itself well to cross-coupling or oxidative transformations. These features mean that the molecule functions as a versatile intermediate—either as a core to append new functional groups or as a scaffold flexible enough for analog synthesis in drug discovery.
We’ve supported teams working on kinase inhibitors, antifungal screening, and selective ligands for biological targets. For these users, trace byproduct analysis matters more than anything printed on a technical data sheet. A standard supply arrangement with one researcher even involved sending pre-packed aliquots under inert gas to keep degradation under control. Learning from their feedback, our team improved stability testing routines, especially since some methylsulfanyl-containing rings can oxidize or decompose unexpectedly during longer storage.
Many of our crop science partners value the selective oxidation pathways available with this molecule. Researchers found that electron-withdrawing effects from the pyridine ring produced higher yields under mild oxidative conditions, an unusual trait compared to other methylthioaromatics. Communication between the synthetic team and in-field testing partners identifies bottlenecks and helps us tweak not just the process, but the packaging and supply arrangements.
In practice, manufacturing oxazolopyridines with alternate substitutions—like ethylsulfanyl, methoxy, or halogenated groups—creates very different challenges. Our process for the methylsulfanyl derivative draws on catalyst selection, reagent purity, and reaction time to avoid problematic side products seen in bulkier or more electron-poor analogs. The methylsulfanyl group’s size and electronic properties directly impact reactivity, especially during late-stage derivatization.
Take 2-ethylthio versus 2-methylsulfanyl analogs: the ethyl version often shows increased lipophilicity and slightly altered melting behavior. In lab practice, methylsulfanyl is easier to handle, purifies with less tailing on silica, and maintains better crystallinity in storage. Substituting a methoxy group often shifts reactivity so much that process modifications become necessary, impacting time, cost, and the risk of byproduct formation. Our production trials revealed lower yields and higher purification burdens for those alternate analogs, with no scalable cost advantage.
Compared to simpler oxazolopyridines lacking the methylsulfanyl group, the 2-methylsulfanyl variant supports richer downstream chemistry. Sulfur functionalization enables oxidations or nucleophilic substitutions that are off-limits in unsubstituted rings. This tailored reactivity often tips the scales for medicinal chemists exploring structure-activity relationships, or for those building new ligands for catalysis.
Feedback from end users continually shifts our internal priorities. For several academic partners, the main concern has been the toxicity profile compared to similar sulfur heterocycles. We provide in-depth trace impurity data, which became especially relevant after some end-users encountered regulatory scrutiny in preclinical filings. Because structurally similar impurities persist from certain oxidation pathways, our QA team collaborates directly with researchers to document impurity fate—especially if the compound enters animal studies.
Storage stability came up repeatedly during international shipments. Early on, we noticed that batch quality dropped when material sat on docks in humid climates. Addressing this issue meant investing in vacuum-sealed, light-blocking packaging, then sharing real-time stability test data with regular customers. Since then, we rarely encounter customer-reported issues linked to degradation during transit, even when shipments cross several time zones and climates.
Industrial scale-up sometimes exposes minor bottlenecks invisible at benchtop scale. Outgassing trends, formation of sticky residues, and dust control turned into recurring topics in scaling runs. Learning from these, we’ve adapted reactor agitation, refined drying steps, and introduced a more robust sieving protocol. The attention to process limitation isn’t just about yields—clean-up time and occupational safety both improve, supporting consistent deliveries to downstream partners on tight production schedules.
Handling methylsulfanyl-oxazolopyridine can sometimes challenge both new and experienced chemists, depending on solvent choice and reaction setup. The compound dissolves readily in polar aprotic solvents and can react vigorously with strong oxidizers, which leads to inconsistent outcomes if dosing speeds or temperature ramps deviate even slightly. We maintain technical bulletins with solvent compatibility, but sharing actual failure cases from pilot or full-scale operations proves most effective for customers scaling beyond gram quantities.
Certain pharmaceuticals and crop protection leads require ultra-low levels of metal impurities. Meeting these high standards often involves post-synthesis treatment that risks product loss—so we built in extra analytics and controlled crystallization at the final stage. Occasionally someone will ask why they see more color or odor variation batch to batch. In these cases, we review core raw material lots for trace sulfur content, since minor fluctuations alter organoleptic properties even after extensive purification.
More than once, customers have faced challenges in solid dispersion or formulation. Our hands-on team supports these partners with practical data: solution-phase stability, achievable particle sizes, and compatibility with common excipients. This is only possible because we keep a portion of each lot for real-world compatibility testing and because the production team routinely exchanges sample feedback with the formulation group.
Safety concerns expand beyond the usual chemical handling protocols. The methylsulfanyl group in this compound, under certain storage or handling conditions, can release sulfurous odors that become problematic in poorly ventilated lab spaces. Though not acutely toxic at low exposure levels, this feature creates compliance and comfort issues, which we address by recommending use in certified fume hoods or dedicated containment vessels during prolonged operations.
Our QA protocols prioritize analysis of polyaromatic and organosulfur contaminants. Whether for regulated pharma or agroscience projects, such contaminants frequently dictate the suitability of an entire lot—not just for safety, but due to compounding effects in multi-step syntheses that follow. We use sensitive chromatographic and spectrometric techniques, collecting and compiling long-term contaminant profiles to inform synthetic improvements and partner reporting practices.
Waste management from the production of sulfur-heterocycles, including 2-Methylsulfanyl-oxazolo[5,4-b]pyridine, calls for practical discipline. Sulfur-containing waste streams pose an environmental challenge, especially for facilities in densely populated or ecologically sensitive areas. Our team works closely with hazardous waste management specialists, tracking disposal and investing in abatement technologies that minimize environmental footprint while complying with regional and international regulations.
Continuous improvement in process chemistry keeps pushing the boundaries of what compounds like 2-Methylsulfanyl-oxazolo[5,4-b]pyridine can achieve. In recent years, novel catalytic transformations have expanded the downstream functionalization options available, particularly for those teams working on next-generation electronics or specialty coatings. Our collaborations with materials scientists sparked a new purification line aimed at producing extra-high-purity lots, where trace transition metals and polar contaminants must be below stringent thresholds.
Innovation isn’t limited to product application. We reinvest in synthetic methods, scaling trials for greener, solvent-efficient protocols that both cut waste and improve product throughput. Pressure from downstream regulatory agencies encourages us to proactively adjust our procedures—so we stay ahead of the compliance curve before it becomes a sales roadblock. Over time, these incremental improvements preserve long-term supply relationships and facilitate faster onboarding for new product development teams looking to trial novel applications.
Trends in data sharing and transparency now drive us to offer complete analytical packages along with each lot, not just once a year for regulatory review. Open communication with research and development partners accelerates troubleshooting and supports application-specific adjustments. By keeping the dialogue open and sharing meaningful analytical trends, we help end-users chart new synthetic territory while mitigating common pitfalls.
As demand for complex heterocycles rises, the niche filled by 2-Methylsulfanyl-oxazolo[5,4-b]pyridine grows both broader and deeper. It finds utility well beyond classic pharmaceutical and agrochemical discovery, extending into advanced materials, analytical reagent development, and catalysis. Our experience has shown that investments in process control, intensive purification, and responsive technical support pave the way for innovation and successful new chemistry.
Practical lessons compound over every production run: controlling input purity, rapidly identifying byproducts, adapting to user-specific application needs, and preparing custom specifications for challenging syntheses. Through direct feedback, analytical collaboration, and a willingness to tweak our processes, we’ve seen this compound help drive forward new discoveries—from the early-stage medicinal chemistry bench, through pilot scaling, all the way to field-ready agricultural trials.
In chemical manufacturing, small changes multiply in impact down the line. By treating customer feedback as an essential metric and prioritizing transparency, adaptability, and safety, we contribute to building a more reliable and productive supply of 2-Methylsulfanyl-oxazolo[5,4-b]pyridine for those who depend on it to discover what comes next.