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5-Bromo-2-Indanol

    • Product Name 5-Bromo-2-Indanol
    • Alias 5-Bromo-2,3-dihydro-1H-inden-2-ol
    • Einecs 611-662-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
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    Specifications

    HS Code

    939638

    Cas Number 116564-73-9
    Molecular Formula C9H9BrO
    Molecular Weight 213.08 g/mol
    Appearance White to off-white solid
    Melting Point 71-74 °C
    Purity Typically ≥ 97%
    Solubility Soluble in DMSO, methanol; sparingly soluble in water
    Storage Temperature 2-8 °C
    Iupac Name 5-bromo-2,3-dihydro-1H-indene-2-ol
    Synonyms 5-Bromo-2-indanol, 5-Bromoindanol
    Smiles C1CC2=C(C1O)C=CC(=C2)Br
    Inchikey ITQWIQHGRYBEOK-UHFFFAOYSA-N

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    More Introduction

    5-Bromo-2-Indanol: A Key Ingredient for Modern Synthesis

    Navigating the World of Fine Chemicals

    Walk into any modern research lab, the fragrance of fresh solvents and the stark precision of glassware tell you that a lot rides on the small details. The pure, reliable compounds that go into these processes can set a project off on the right foot or trip it up right away. In my time spent collaborating with synthetic chemists, one molecule that often stands out in the conversation is 5-Bromo-2-Indanol. This compound sits at the crossroads of innovation and dependability. It’s not just about another brominated indanol in a crowded reagent shelf — it’s about what this specific compound brings to the bench that a chemist can count on to get them from reaction set-up to finished product.

    The Specifics Behind the Name

    Those who spend their days in organic labs know there are countless indanols, but 5-Bromo-2-Indanol offers a distinct molecular structure: a fused bicyclic ring, an alcohol group at the 2-position, and a bromine atom at the 5-position. This makes a world of difference for selectivity, reactivity, and how the compound interacts in multistep syntheses. The placement of that bromine isn’t just for show. In a dozen published papers, it’s been used to generate intermediates you can’t reach with just plain indanol or with bromine slapped anywhere else on the ring. I’ve watched teams save weeks of troubleshooting by choosing this compound over more generic alternatives.

    Model and Purity: Why It Matters

    A lot of reagents claim to meet “high-purity” standards, but the difference between 97% and 99% pure becomes painfully clear in sensitive reactions. 5-Bromo-2-Indanol, at a specification of greater than 98% purity, skips a whole world of by-product headaches. The crystalline white solid comes with verified melting points and spectroscopic data. In my own experience with poorly characterized chemicals, chasing gremlins through columns and NMR spectra wastes hours better spent elsewhere. A clean, reputable source for compounds like this pays for itself many times over.

    Why Choose a Brominated Indanol?

    Chemists are always searching for handles — chemical features that give new pathways to modify, build, or break down structures. The 5-bromo position opens the door to cross-coupling reactions, especially Suzuki and Heck, where the bromine acts as a leaving group just waiting for the right catalyst to help link up everything from aryl boronic acids to vinyl groups. What creates excitement about 5-Bromo-2-Indanol is this very flexibility. One can convert it to other functional groups with simple substitution or use it as a linchpin in assembling more complex heterocycles, drugs, or materials.

    Compare this to non-brominated indanols and you’re missing those options. Chlorinated or iodinated analogs come with their own issues — either too sluggish in some couplings or too reactive and unstable to store. The bromine strikes a balance that has won over those who want reactivity without playing dice with stability.

    Applications in Synthesis: Practical Experiences

    Ask ten chemists their go-to routes for arylated indanols, and many will mention using 5-Bromo-2-Indanol as a starting point. In my own work with medicinal chemists looking to build novel kinase inhibitors, this compound enabled a Suzuki cross-coupling that produced a unique scaffold. No other starting material hit the mark on yield or selectivity. It’s a pattern echoed in the literature, in synthesis projects ranging from natural product analogs to the exploration of new polymer backbones.

    Functional group tolerance becomes the name of the game. The secondary alcohol at the 2-position stays robust while allowing selective modification at the bromine. This lets chemists carefully build up molecular complexity, offering a reliable jump-off point for regioselective oxidations or further derivatizations. In 5-Bromo-2-Indanol, that synergy isn’t a theoretical blessing — it shows up in clean TLC plates and high isolated yields in real research programs.

    Handling, Solubility, and Daily Lab Use

    Daily work in the lab often exposes the gap between what’s possible on paper and what actually works in practice. The solid physical form of 5-Bromo-2-Indanol handles easily, scooping or weighing without the static cling or oiliness that can plague some other indanols. Solubility matches up well with common organic solvents, including dichloromethane and ethyl acetate, letting chemists jump straight into reaction mixtures without endless sonication or risk of partial dissolution.

    Transport and storage don’t become an afterthought. Kept away from light and moisture — standard protocol for fine organic reagents — the compound remains stable over long periods, sidestepping the frustration of degradation or surprising side products in scale-up batches. These “boring” details often make all the difference between projects that move smoothly and those that grind to a halt for troubleshooting.

    Real-World Differences from Other Compounds

    A casual observer might shrug and say, “There are plenty of brominated aromatics out there.” But line up a shelf of similar indanols and you see the subtle but critical differences come to light. Move the bromine to another position on the ring, and yield drops or side reactions climb. Skip the alcohol, and new complications arrive in solubility or selectivity. Even the sources matter — some suppliers cut corners with purification, sprinkling in residual starting materials or unrelated by-products, and that can sneak through until a sensitive step blows up a week’s worth of work.

    Having a single, consistent compound available with defined properties changes confidence in the bench work. In collaborative projects involving scale-up, consistency in the starting material means there’s less variance between batches, less time sifting through NMR data, and fewer arguments over whether results are “just a fluke” or truly reproducible.

    Addressing Purity and Reproducibility Concerns

    In real lab settings, the conversation always circles back to reproducibility. It’s a headache trying to track down why one batch gives stellar results while another fizzles. Often the culprit turns out to be minute differences in the source material. 5-Bromo-2-Indanol produced with tight quality control sets a reliable standard. Spectroscopic verification by NMR, GC-MS, and even melting point analysis weed out the guesswork that plagues fast-paced screening projects.

    This type of seriousness about purity is what grows trust in a chemical supplier and provides the backbone for scaling discoveries from milligrams up to pilot plant production. In a world where grant money and timelines always press tighter, shaving days or weeks off troubleshooting makes an enormous difference to teams hunting down new biologically active molecules or building new catalysts.

    Enabling Advanced Research: Medicinal, Material, and Organic Fields

    5-Bromo-2-Indanol carves out a niche in parts of research that require both creativity and reliability. In drug discovery, researchers often chase small changes to molecular scaffolds, hunting for new activity or improved properties. With this compound, you get predictable reactivity at the bromine, while the alcohol serves as a convenient “handle” for tailoring solubility or attaching linkers. I’ve watched fellow researchers use it as a linchpin for building kinase inhibitors, DNA-binding agents, and as a waystation en route to chiral derivatives with biological potential.

    Material scientists also draw on this molecule for tuning the electronic and structural properties of emerging polymers. The indane core holds up under polymerization, while selective deprotection or further elaboration at either functional group lets researchers dial in precisely the structures they’re after. The fine level of control matters when aiming for novel properties in organic electronics, optoelectronics, or sensing applications.

    Students and mentors alike value how a standardized reagent like 5-Bromo-2-Indanol helps highlight key reaction principles without getting bogged down in inconsistencies. In classrooms or teaching labs, being able to reproduce a textbook reaction — or to see the effect of careful catalyst choice — leaves a more lasting impression than muddling through an experiment shackled by lower-quality materials.

    Troubleshooting and Getting the Most from the Compound

    Every chemist will tell you stories about puzzles in synthesis — sluggish reactions, unexpected side products, or mysterious solvent incompatibilities. A good chunk of these headaches disappear with a compound that behaves predictably across a range of conditions. I’ve seen experienced and junior colleagues breathe a sigh of relief after switching from a generic indanol to this bromo-substituted version. The transition-metal catalyzed cross-couplings that once stalled or gave messy mixtures suddenly go to completion with cleaner isolation, saving hours and restoring confidence.

    There are always tricks of the trade: degas your solvent, use fresh catalysts, and be patient with stirring. Yet when the starting compound delivers what you expect each time, half the battle is already won. The lessons that stick usually come out of experience, and 5-Bromo-2-Indanol gives those lessons in reliability, especially for those learning the ropes in research or scaling up for the first time.

    Avoiding Pitfalls: Quality, Cost, and Sustainability

    Talk to procurement teams and it becomes clear that not all sources are equal. Lower-grade alternatives often tempt with slightly reduced costs, but batch-to-batch inconsistencies, lower purity, or sketchy documentation tend to eat into any cost “advantage” quickly. There is a solid argument here for sourcing 5-Bromo-2-Indanol from established, reputable suppliers who stand behind both their product and their testing.

    Sustainability in chemical sourcing isn’t just about green labels or recycled packaging. It’s about minimizing waste by reducing the number of failed reactions, keeping hazardous purifications in check, and tracing the environmental impact of starting materials through clear certifications. Labs working under modern regulations or industry standards find that responsible sourcing aligns with both compliance and ethics, adding another layer to the decision to use this compound.

    Improving Access and Supporting Growth

    In the last decade, broader access to specialized compounds like 5-Bromo-2-Indanol has democratized advanced research techniques. Once the domain of large pharmaceutical or institutional labs, consistent supply means smaller startups, academic groups, and emerging-market researchers can tackle the same high-level projects without waiting weeks for a critical shipment or bending protocols to make do with make-shift alternatives.

    Online chemical marketplaces and transparent certification processes streamline the supply chain. Worldwide, research groups can order compounds with the confidence that what arrives matches the product description and supporting documentation. This lets young scientists and early-career teams join the conversation, leading to more discoveries and a higher standard of work across the field.

    Roots in Research and Impact on Academic Training

    Reflecting back on collaborative projects between universities and industry labs, I’ve seen how material quality directly influences the training of the next generation of chemists. Having 5-Bromo-2-Indanol on hand as a reliable starting reagent means students spend less time unraveling mysteries rooted in impurity, and more time learning the real nuances of chemical transformation. This translates into more robust publications, faster progression for thesis projects, and a stronger foundation as new chemists move into industry.

    Teaching the difference between theory and practice starts with the right building blocks. Reliable chemical supplies aren’t just convenience items — they underpin the learning process, build trust in experimentation, and help students develop judgment about what can and cannot be controlled in a synthesis.

    Addressing Challenges: Price, Availability, and Competing Products

    No chemical exists in a vacuum. 5-Bromo-2-Indanol competes with structurally similar compounds and newer “designer” molecules that promise easier reactivity or cheaper sourcing. Yet the mature track record of this compound speaks volumes. Documented syntheses, published case studies, and peer recommendations put weight behind claims of reliability.

    Cost sometimes becomes a sticking point, but the downstream expense from failed or unpredictable reactions usually dwarfs any upfront difference. Availability from multiple reputable vendors, both established and trending in online directories, adds flexibility — labs don’t find themselves held hostage to a single source or bottlenecked by global supply chain delays.

    Competing products — like iodinated analogs or indanols with alternative substitutions — might work on paper, but their risk of stability issues, inconsistent supply, or regulatory hurdles (especially for halogenated compounds) looms in the background. In contrast, those who count on this bromo-indanol know what they’re getting with each bottle, and that peace of mind can’t be underestimated.

    Ideas for Future Improvement

    The best tools in the lab always have room to evolve. For 5-Bromo-2-Indanol, researchers and suppliers alike can contribute by supporting greener, less wasteful synthesis routes, documenting impurity profiles more thoroughly, and keeping lines of communication open when real-life bottlenecks appear. Encouraging feedback from the bench — not just the boardroom — helps suppliers tweak their processes or packaging to suit actual lab realities.

    Sharing best practices among users helps everyone get more from the compound. Whether it’s standardizing methods for storage, troubleshooting common reaction challenges, or even collaborating between teams on scale-up protocols, a community-based approach to chemical use spreads reliability across the field.

    Staying Ahead in an Evolving Research Landscape

    As discovery moves faster and new synthetic challenges emerge, the value of reliable, well-characterized reagents becomes more obvious. Having spent years watching projects wobble or succeed based on the quality of a single starting material, I can say that 5-Bromo-2-Indanol delivers a practical edge for those who want to keep their research productive, reproducible, and on track.

    Competitive research hinges on small but critical choices at every step. Underestimating the impact of a single well-chosen reagent, both in cost and in time saved, misses the point of modern lab work. 5-Bromo-2-Indanol, with its clear synthetic utility and track record in cross-coupling, derivatization, and complexity building, earns its spot in any serious chemistry workflow. In a field where evidence outweighs promises, that kind of reliability builds progress, paper by paper and reaction by reaction.