|
HS Code |
595469 |
| Cas Number | 74241-09-9 |
| Molecular Formula | C4H2BrClS |
| Molecular Weight | 213.48 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 206-208°C |
| Density | 1.816 g/cm3 |
| Purity | Typically ≥ 98% |
| Solubility | Insoluble in water; soluble in common organic solvents |
| Refractive Index | 1.592 |
| Synonyms | 2-bromo-3-chlorothiophene |
| Smiles | Brc1sccc1Cl |
| Inchi | InChI=1S/C4H2BrClS/c5-3-1-2-7-4(3)6 |
| Flash Point | 96°C |
| Storage Temperature | Store at 2-8°C |
As an accredited 2-Bromo-3-Chlorothiophene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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| Shipping | |
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Talking chemistry means recognizing the workhorse molecules that push innovation forward. Among these, 2-Bromo-3-Chlorothiophene has secured a spot for anyone aiming to build out thoughtful synthesis or custom molecules for complex projects. This compound, bearing the CAS number 14258-36-7, brings together a bromine and a chlorine on the five-membered thiophene ring, resulting in a molecule that stands out for both its reactivity and selectivity.
One quick look at the structure tells a trained eye plenty. The arrangement—bromine at the second position, chlorine at the third—changes what can be done with the thiophene core. With a molecular formula of C4H2BrClS and a molecular weight sitting close to 215 g/mol, it finds balance between bulk and manageability. This is not an off-the-shelf raw material, as the two halogens ask for careful handling and thoughtful application. Reliable supply means consistent color, typically ranging from pale yellow to light brown due to its electronic properties and stability under ambient conditions.
Purity matters when reactions can spin out of control with a minor impurity. Most quality-driven suppliers focus on getting 2-Bromo-3-Chlorothiophene delivered at purities above 98%. Chromatographic and spectroscopic data back up these numbers, not just paperwork. In the lab, proper sealing and storage in cool, dry areas keep the compound in top shape for its next transformation.
Diving into real-world use, this molecule serves as a building block in pharmaceutical research as well as in electronics and advanced materials. I remember colleagues wrestling with complex synthesis, searching for partners that would open the ring for new possibilities or set up cross-coupling reactions. Having both bromine and chlorine atoms on the same ring stretches what’s possible in Suzuki, Stille, or Heck reactions. This sort of flexibility cuts down on steps, increasing atom economy and often making synthesis more sustainable—an important angle as material scientists and chemists chase greener routes.
In pharma, side chain modification sometimes means everything to the success of a small molecule drug candidate. The dual halogen pattern within this molecule invites selective reactions at each site, often unlocking novel analogues or helping attach a fluorophore or a moiety to boost efficacy or bioavailability. Talking with research teams, I’ve seen breakthroughs hinge on finding exactly the right starting material—something offering selective activation and reliable downstream chemistry. 2-Bromo-3-Chlorothiophene supports that work without demanding drastic new protocols.
Working with thiophene derivatives, I’ve noticed that each subtle swap of halogen or substituent opens new doors. 2-Bromothiophene and 3-chlorothiophene stand as close relatives, yet each one behaves differently when faced with metal-catalyzed cross-couplings or nucleophilic substitutions. The difference: positional effects and the electron-withdrawing strength of bromine and chlorine.
In straightforward terms, many only see the halogen atoms as placeholders for further chemistry, but placement makes a world of difference. If the goal is regioselective functionalization, 2-Bromo-3-Chlorothiophene outshines more simply substituted thiophenes. The bromine at the second position is reactive toward palladium-catalyzed couplings, while the chlorine often stays patient, allowing for sequential transformations. This means multi-step synthesis can proceed with fewer purification headaches, a real breakthrough for teams dealing with tight deadlines and limited budgets.
Anecdotes from process chemists reinforce this. They share that switching out a thiophene for this bromo-chloro derivative condensed steps and improved yields. For OLEDs and small-molecule semiconductors, the stability and controlled substitution that comes with this scaffold make it an attractive precursor for high-performance materials.
Any discussion about substituted thiophenes should also acknowledge what comes with those halogens. Potential environmental and safety implications can’t be brushed off. As someone who has logged many hours reviewing these issues for EHS compliance, I can say that evaluating the downstream effects of producing and handling bromo- and chloro-compounds is crucial. Even a valuable synthetic tool must be handled with protocols that protect the workforce and environment.
Controlling emissions and waste isn’t a box-ticking exercise. Smart companies invest in capture and recycling technologies for halogenated byproducts, lowering the impact of their operations. In research settings, minimizing waste comes from running reactions at the smallest practical scale, using green solvents or alternatives like supercritical CO2 when possible, and always planning for safe disposal.
Real progress doesn’t come only from using smart chemistry; it depends on fair access and clear expectations for cost. Having coordinated with procurement and lab managers, I’ve seen debates about the cost-benefit of higher purity or specialized intermediates. 2-Bromo-3-Chlorothiophene sometimes carries a premium, but the reduction in failed runs, rework, and lost time quickly balances the books if the project demands precision.
I remember testing suppliers with a focus on transparency—Requesting up-to-date COAs, asking about lot-to-lot consistency, and requesting details about transport. Responsible suppliers provide certificates attesting to purity, trace impurities, and compliance with local regulations. Labs working in regulated industries, like pharmaceutical synthesis, often require even more stringent traceability to build a complete data package for their regulatory filings. Suppliers who cut corners or refuse to document proper handling shouldn’t be in the conversation when lives or mission-critical devices depend on reliable chemistry.
Some might see 2-Bromo-3-Chlorothiophene as just another specialty chemical, but this misses the real value. The complexity it offers in molecular design pushes researchers past incremental tweaks into more ambitious synthesis and discovery. The molecule’s ability to open up unique ring structures or access derivatives with peculiar properties marks it out as more than just a background reagent.
In one materials project, a decision to pivot from a mono-halogenated thiophene to this bromo-chloro alternative produced a step-change in both yield and stability of the end product. Project leads pushes their teams to reconsider base assumptions about starting materials, looking for competitive advantage in every carbon and heteroatom placement. The difference ends up tangible, not abstract.
Academic researchers also gravitate to compounds like this in mechanistic studies. The natural differences in reactivity between the bromine and chlorine set up intelligent testing grounds for understanding selectivity and reaction optimization. I’ve seen graduate students thrive on these challenges, learning the hard way that every structural motif carries its own story in reactivity and application.
With ambitious sustainability targets emerging from industry and academia, more chemists are taking a new look at traditional building blocks. 2-Bromo-3-Chlorothiophene often features in conversations about replacing less selective precursors that can lead to higher waste or inferior atom economy. Greener processes might involve leveraging one-pot or telescoped reactions to minimize solvent use and avoid dangerous workups.
I’ve sat in group meetings where these issues shift from theoretical to practical—how do you take the best of what this molecule can offer, without leaving a bigger footprint behind? Some teams use alternative coupling strategies that allow milder conditions, reducing both energy and waste. Others scrutinize purification, using advanced filtration or crystallization instead of relying on large volumes of halogenated solvents. It’s rarely perfect, but each small tweak gets teams closer to the goal of sustainable innovation.
Handling bromo- and chloro-compounds isn’t just about knowing the numbers on the MSDS. Practical lab routines—like weighing out powders in a fume hood, changing gloves often, and tracking usage in a notebook—matter as much as any official guideline. From personal experience, keeping containers tightly closed and dry is no small matter. The pungency of these chemicals means a spill or improper disposal is noticed right away.
Institutes and companies that get this right invest in clear training, routine inspections, and strong peer support, not just paperwork. Beyond standard lab PPE, designated disposal containers for halogenated waste make a difference, and every team member knows not to shortcut the process. In my time mentoring new researchers, I stress that the best science often comes out of the safest lab, where risks are managed openly and problems are caught before they grow.
Quality control gains new importance in a world of global supply chains. Strong data on lot consistency, impurity profile, and traceability makes the difference between hassle-free batch releases and headache-inducing investigations. In custom syntheses or pharma applications, unchecked impurities could derail whole projects.
Connecting with QA colleagues, I’ve learned the value of robust documentation and transparent record-keeping. Teams should demand detailed COAs that include not only purity figures but also known trace contaminants, typical solvent residues, and even the batch’s production route when available. Competent suppliers update clients about changes in production protocol, raw material sources, and relevant regulatory updates. Open communication prevents surprises at later stages and keeps innovation moving without interruption.
Supply issues can torpedo a project. It’s not enough for a compound like 2-Bromo-3-Chlorothiophene to wow a synthetic chemist on paper; the real measure is whether it shows up on time, meets quoted specs, and makes it through customs without drama. This means taking a hard look at vendor partnerships and thinking long-term.
One recurring lesson: investing a little time up front choosing the right supplier beats endless rounds of troubleshooting on subpar lots. Solid working relationships ease the tension when timelines get tight or special documentation is needed. Even with more niche compounds, competent suppliers help clients navigate customs, logistics hurdles, and regulatory paperwork. This matters as teams move beyond the pilot stage into greater scale, and the cost of disappointment only grows.
As synthetic targets grow in complexity—especially in pharma and advanced materials—the expectation grows for building blocks that offer more than just standard reactivity. 2-Bromo-3-Chlorothiophene meets this demand, providing selective entry points for functionalization that less sophisticated thiophenes just can’t match.
Medicinal chemists and materials scientists increasingly lean on molecules like this to shortcut multiple-step syntheses, increase signal in functional assays, or tune the electronic profile of a new polymer. These are not always visible in the final product, but their influence runs deep through every stage of discovery. My own experience teaches that fresh solutions often come from using a new building block at the right moment, not just tweaking conditions on a familiar scaffold.
Despite all its benefits, 2-Bromo-3-Chlorothiophene doesn’t escape the core challenges of modern chemistry. The cost and difficulty of producing highly pure material at scale, keeping quality stable, and managing environmental impact are ongoing battles. Companies and academic groups committed to continuous improvement take stock regularly, run pilot trials with new protocols, and push vendors for process upgrades.
Innovations in flow chemistry and continuous processing show promise for scaling up production while limiting waste and energy use. Automated monitoring—especially with inline NMR or IR—helps producers keep a tight rein on process purity and safety. Bringing together chemical know-how, automation, and real accountability, the gap between bench-scale synthesis and commercial supply starts to close.
The people working at every step—from R&D to shipping—make the difference. Fielding feedback from clients, organizing joint troubleshooting sessions, and sharing lessons learned build real resilience into the supply chain. That’s how the molecule shifts from just another option in a catalog to a reliable foundation for new discoveries and steady progress.
2-Bromo-3-Chlorothiophene deserves its reputation as a flexible, robust, and highly useful building block. With the right vision, a research group or company leverages it for efficiency, lower waste, and deeper innovation. Pursuing progress means staying engaged at all levels—from the technical details of handling and reactivity, through safety and compliance, to the bigger question of sustainability.
Staying current with the latest protocols and best practices, pushing for more transparent supply chains, and sharing honest feedback with suppliers and peers collectively drives chemistry forward. My experiences, and those of many peers, suggest that tools like 2-Bromo-3-Chlorothiophene aren’t just stopping points in discovery—they’re springboards to more ambitious, effective, and responsible work.