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HS Code |
227569 |
| Product Name | 2-(5-Bromopyridin-2-Yl)-2-Propanol |
| Cas Number | 153559-49-0 |
| Molecular Formula | C8H10BrNO |
| Molecular Weight | 216.08 g/mol |
| Appearance | White to off-white solid |
| Solubility | Soluble in organic solvents like DMSO and methanol |
| Purity | Typically ≥ 98% |
| Smiles | CC(C)(O)C1=NC=C(C=C1)Br |
As an accredited 2-(5-Bromopyridin-2-Yl)-2-Propanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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People might not recognize the name 2-(5-Bromopyridin-2-Yl)-2-Propanol right away. In practice, this chemical plays a behind-the-scenes role in the world of drug development and laboratory research. I’ve seen it used in settings where reliability and precise reactivity count for more than just laboratory theory. Chemists and analysts seek it for its unique combination of stability and reactivity, which many other pyridinyl compounds can’t quite match.
Looking at its structure, you find a pyridine ring with a bromine atom at the fifth position, and a secondary alcohol group tethered at the second. While this chemistry lesson takes folks back to organic class, the placement of bromine alters both its reactivity and how it interacts with other chemicals. A well-made batch should present as a colorless to pale yellow crystalline solid, sometimes appearing slightly tan depending on trace impurities, but any experienced chemist can spot the purity based on physical trait and melting point.
Reputable laboratories publish a purity above 98% for usable 2-(5-Bromopyridin-2-Yl)-2-Propanol, which allows for consistent and reliable downstream chemistry applications. The melting point typically ranges from 76°C to 81°C; deviation means possible problems. Selective solubility makes it workable in systems based on dichloromethane, methanol, or dimethyl sulfoxide, while insolubility in water prevents certain unwanted side-reactions. I’ve seen how solubility choices play a major role in chemists’ protocols—if a compound is too stubborn, it wastes time and energy. This one earns its keep by cooperating with routine lab solvents.
In the pharmaceutical world, intermediate steps lay the foundation for complex molecules. For medicinal chemists, 2-(5-Bromopyridin-2-Yl)-2-Propanol serves as more than just a link in the chain—it’s a starting block for synthesizing novel pyridine-based pharmaceuticals. Because the bromine in the five-position creates a handle for further chemical modification, the compound becomes valuable for targeted reactions such as Suzuki-Miyaura and Buchwald-Hartwig couplings. These transformations open the door to a world of nitrogen-containing drugs and investigational agents.
It isn’t just about the chemistry, though. Stories from people in the lab underscore the time saved during purification steps, thanks to its pronounced secondary alcohol group, which allows for easier separation and clear tracking via common analytical tools. In my own routine, the combination of functional group diversity and bromine reactivity translated directly into fewer failed reactions. While many other precursors create headaches when purification brings surprises, this one usually offers predictability, making it a safe bet for tight project timelines.
This isn’t just another pyridine derivative shuffled off a generic catalog. Countless compounds crowd the shelves at any research facility; some prove too touchy, and others lack the flexibility demanded by multi-step organic syntheses. 2-(5-Bromopyridin-2-Yl)-2-Propanol stands out because it gives researchers precise control in forming bonds at the five position, while the secondary alcohol keeps open further downstream options—oxidation, protection, or even more elaborate derivatization.
Compared to simple pyridine alcohols, which can be limited by lower reactivity, the addition of bromine opens up reactions a chemist can’t otherwise access. Other halogenated pyridines sometimes introduce unwanted toxicity or side-reactions, but the careful placement here avoids that. Too often, alternatives come with hidden headaches: they might degrade under common reaction conditions, or they bleed into chromatographic separations, costing precious time and resources. Over the years, I have learned to appreciate materials that help avoid that sort of waste.
Every research group searching for better kinase inhibitors, anti-infectives, or brain-penetrant drugs benefits from versatile intermediates. 2-(5-Bromopyridin-2-Yl)-2-Propanol fits this mold by bridging the gap between bench chemistry and real-world clinical needs. Its backbone appears in lead optimization efforts where any structural nick or scratch may alter biological activity.
This isn’t just theory. Patents list it as a precursor when building novel compounds with anti-cancer properties. Startups and university labs use it for small-run pilot reactions where speed matters—a detail I first encountered during a tricky SAR (structure-activity relationship) campaign. Armed with a batch of this substance, we managed to generate a series of analogs in days instead of weeks, which made a world of difference in hitting milestones and moving toward preclinical testing.
Every professional with hands-on experience knows the basics: store in a cool, dry place away from incompatible materials, and use appropriate gloves and eye protection during handling. I remember early years where more than one project slowed down because careless handling contaminated an entire batch of expensive reagent—lessons learned the hard way. This compound fares well in long-term storage if sealed from the air, as its crystalline form resists both oxidation and moisture uptake compared to more sensitive analogs.
No chemical can claim zero hazards; standard MSDS guidance applies, especially with halogenated aromatics. Most colleagues report minimal odor and a non-hygroscopic nature, which makes it a relief compared to heavy oils or low-melting impurities. Spills and clean-ups prove straightforward if common protocols are used. Once the bottle finds a spot in the chemical cupboard, it tends to stay there for repeat reactions.
Not every shipment delivers the same experience. Variability in suppliers often translates into headaches downstream. I’ve watched senior chemists send back half a dozen hundreds-gram bottles because off-color solids or marginal NMR readings flagged something that failed QC. Choosing high-quality material not only protects the project, but also maintains safety in the lab. A few reputable providers publish full analytical profiles so researchers can verify purity before use, which I consider indispensable. With knock-off products, you can never be sure that trace contaminants won’t sabotage yields or cause mysterious byproducts.
This compound’s popularity means a steady supply on the open market, but shortcuts tempt some producers. I’ve run enough reactions to value a full set of HPLC, NMR, and GC-MS data for every batch. In a field where an impure intermediate can sink a whole route, a small investment in qualified material saves much more in the long run.
I’ve talked to other chemists who swear by this compound for screening projects where limited material and tight budgets force hard decisions. The ease of introducing functional diversity with this intermediate means more hits, faster optimization, and fewer bottlenecks. Researchers in both academia and industry point to the difference it makes in iterative medicinal chemistry cycles, where each generation of analogs matters. The ability to quickly install new groups at key positions streams lines discovery and derisks the development process.
One colleague told me his team landed a promising kinase inhibitor after switching to this intermediate, which helped them steer away from a dead-end route with a less adaptable precursor. Another recounted an instance where a competing analog, lacking the secondary alcohol, stalled under mild conditions and failed to deliver even after repeated troubleshooting. These anecdotes echo what many synthetic chemists might say after years dodging avoidable complications.
Markets for specialty chemicals continue to evolve. With artificial intelligence and automation taking firmer root in experimental design, the demand for high-purity, versatile intermediates like 2-(5-Bromopyridin-2-Yl)-2-Propanol only grows. Traditional bench trial and error meets algorithmic speed, amplifying the need for compounds that foster rapid, reliable reactions across broad chemical space.
I’ve seen requests for large-scale delivery spike as more contract research organizations (CROs) enter the fold. What used to be a niche supply chain now attracts attention from global buyers tracking tight regulatory standards and seeking traceability for critical intermediates. The trend isn’t slowing down, and those in procurement and supply need to make good choices in sourcing—rushed, inconsistent batches impact both cost and credibility.
Sustainability concerns also come to the forefront. End users ask for details about precursor sourcing, byproducts, and waste profiles. One group I worked with spent much of last year probing greener alternatives and optimizing conditions to minimize halogenated waste. Advances in synthetic route design may shift reliance from more hazardous reagents to milder, catalyzed steps. 2-(5-Bromopyridin-2-Yl)-2-Propanol stands out for not needing exotic catalysts or heavy metals for many applications; reactions often proceed under milder conditions, reducing both environmental impact and operator risk.
Let’s face it: no specialty research chemical is free from practical headaches. One recurring issue involves mislabeling or receiving product outside listed specifications. Researchers who double-check every delivery avoid costly surprises. In situations where process scale-up exposes new risks, partnering with suppliers who offer transparent, batch-level documentation gives teams the confidence to press forward. Analytical cross-checking— including TLC, NMR, and melting point confirmation —remains a wise step, even if the certificate of analysis looks flawless.
Logistics sometimes throws a wrench into even the best-laid plans. I once watched a time-sensitive shipment stuck at a customs checkpoint for days because the paperwork listed a nonstandard trivial name. Direct, ongoing communication with couriers and customs agents can often head such mishaps off. Organizing reorder points and keeping a small buffer supply on hand can save a project from grinding to a halt during unexpected global supply chain hiccups.
Another issue comes up when switching between small-scale and bulk reactions. Solvent ratios, heating rates, and purification procedures need re-optimization to keep yields high. Open dialogue between bench chemists, process engineers, and QA staff helps capture those tweaks that might not make it into formal lab records. The teams that build adaptation into their workflow keep surprises small and learning curves gentle.
Budget limitations remain real, especially in startup settings or public research centers. Chasing the lowest price often backfires. A cheaper source might save money upfront but hidden costs—lost time, failed reactions, and safety risks—stack up. During a grant-funded project, we learned the hard way that low-quality intermediates could set our schedule back months. Investing more for verified, reproducible quality delivered compounding returns: higher success rates, fewer hours spent troubleshooting, and wider adoption of our synthetic methods by others.
Quality control doesn’t only sit at the supplier’s door. In-lab checking builds a layer of trust and a baseline for troubleshooting. Culture grows when teams value decision-making based on sound analytical verification rather than trust in branding or anecdote. Each time a group pushes innovation, the right intermediates can shift the trajectory of the whole project.
Emerging chemical informatics tools now help predict potential batch-to-batch variation, picking up where instinct and experience leave off. By integrating automated quality checks into the workflow, research organizations minimize guesswork and increase reproducibility.
Success in cutting-edge research no longer rides only on the shoulders of individual chemists, but on the quality of their starting materials. As medicinal chemistry pivots toward multifunctional scaffolds and step-efficient building blocks, demand grows for intermediates like 2-(5-Bromopyridin-2-Yl)-2-Propanol. Its unique structure lays the groundwork for sophisticated molecular architectures without closing off future modification routes.
Training new generations of synthetic chemists also means handing them tools that work as advertised. There’s value in intermediates that don’t blindside users with unexplained reactivity or problematic side-products. My own teaching moments start with substances like this, where reliability lets students focus on learning reaction theory and troubleshooting protocols rather than salvaging spoiled reactions.
The compound’s versatility helps diverse projects thrive, from early-stage medicinal chemistry to process optimization. Teams intent on shortening cycle times find themselves returning to trusted reagents that make work more predictable and creative at the same time. This intersection— between robust execution and flexible application— defines what separates a helpful intermediate from just another reagent on the storeroom shelf.
Consensus among experienced professionals points to the added value of reliable, functionalized intermediates. 2-(5-Bromopyridin-2-Yl)-2-Propanol brings measurable impacts on efficiency and success across a spectrum of innovation efforts. During challenging times— limited access to global suppliers, changing regulatory standards, rising demand for transparency— dependability in sourcing and application has never mattered more.
Many organizations prioritize open communication between procurement, research, and quality assurance. The best results follow from careful vetting and honest collaboration— whether the goal is a first-in-class therapy or a smarter process for known pharmaceutical targets. By sticking to tried-and-true intermediates paired with innovation-driven protocols, teams set themselves up for both quick wins and long-term gains.
Everything comes back to the basics: understanding what a compound can and cannot do, making choices based on a blend of science, experience, and verified data. 2-(5-Bromopyridin-2-Yl)-2-Propanol earns its place in the modern researcher’s toolkit by offering more than just a chemical formula. It answers practical needs for reactivity, reliability, and flexibility where so many alternatives fall short.
As field expectations shift toward higher standards and accountability, those who embrace better materials and data-driven decisions will lead the way. Countless researchers, from early-career postdocs to seasoned principal investigators, return to this intermediate not out of habit, but because it gets the job done efficiently. Projects stay on course, learning accelerates, and teams meet strict milestones in an environment where wasted effort carries a real cost.
Long hours at the lab bench teach you what’s worth trusting. This compound— with its thoughtful design and proven utility— stands as a quiet but crucial partner behind scientific discovery and innovation.