|
HS Code |
282765 |
| Chemical Name | 5-Bromoquinazolin-4-One |
| Cas Number | 77510-68-0 |
| Molecular Formula | C8H5BrN2O |
| Molecular Weight | 225.05 g/mol |
| Appearance | Off-white to light brown solid |
| Melting Point | 230-235°C |
| Purity | Typically >98% |
| Solubility | Slightly soluble in DMSO, ethanol |
| Storage Conditions | Store at 2-8°C, dry and dark |
| Smiles | C1=CC2=C(C=C1Br)C(=O)N=CN2 |
| Inchi | InChI=1S/C8H5BrN2O/c9-5-1-2-6-7(3-5)11-4-10-8(6)12/h1-4H,(H,10,11,12) |
As an accredited 5-Bromoquinazolin-4-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | |
| Shipping | |
| Storage |
Competitive 5-Bromoquinazolin-4-One prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
In the modern world of organic synthesis, 5-Bromoquinazolin-4-One stands out for those searching for reliability and distinct chemical performance. This compound often enters the conversation in research labs working on pharmaceutical intermediates, agrochemical prototypes, and custom synthesis projects. Its unique quinazoline core, highlighted by a bromine at the fifth position, draws interest for its potential role in new drug discovery and synthetic pathways.
Working with countless reagents through the years, I have always respected the consistency and clarity certain core intermediates provide to a development process. 5-Bromoquinazolin-4-One delivers a clear standard in quinazoline chemistry, giving chemists a foundation where new functional groups can be introduced or reactions can be planned with less uncertainty.
Reliable research needs dependable materials. Every chemist knows that a poorly characterized intermediate brings frustration and wasted time. 5-Bromoquinazolin-4-One, when sourced from trustworthy suppliers, forms pure, off-white to pale yellow powder, melting typically around 245-248°C. These simple physical cues go a long way to signal purity. Any deviation here, such as unexpected hue or melting range, suggests trouble before reactions even begin.
My own experience has taught me the real value of sharp melting points and visible purity in a benchtop sample. It makes analytical work less arduous and gives a scientist more confidence when running follow-up reactions. Unexpected contamination from cheap knockoffs or poorly controlled batches rarely stops with yield loss—it usually seeps into chromatograms, upends reaction plans, and stifles innovation.
Every tool has its use. In the search for new anti-inflammatory compounds or modified kinase inhibitors, 5-Bromoquinazolin-4-One provides an effective building block. Its quinazolinone framework forms the nucleus for ligand design across medicinal chemistry. Laboratories looking for a substrate with high reactivity and easy substitution at the fifth position often turn to this compound because bromine serves as a handy leaving group under Suzuki or Buchwald-Hartwig conditions.
In my early days, I wrestled with halogenated heterocycles that failed to react or plagued reactions with later-stage side products. Once I found a reliable 5-Bromoquinazolin-4-One supplier, the shift was obvious—purer outputs, fewer side-products, easier purification, and streamlined downstream workup. Small tweaks like these, especially when scaling from milligrams to grams, impact everything from timeline to publication speed.
Many intermediate quinazolinones line chemical catalogs, but brominated analogs like this one solve some old lab headaches. While classic 4-quinazolinones remain rigid and tough to diversify, putting a bromine ring lets researchers attach various functional groups quickly. Bromine’s size and reactivity, especially in palladium-catalyzed couplings, lowers the barrier for medicinal chemists dreaming up challenging molecule designs.
Compare this experience with using iodo- or chloro-quinazolinones. Chloro-derivatives might sound cheaper, but they react sluggishly and often force researchers to crank up temperatures, risking decomposition. On the other side, iodo-quinazolinones ask for careful storage and can sometimes lead to uncontrolled side-products. 5-Bromoquinazolin-4-One’s middle-ground reactivity keeps reactions efficient, yet controlled, giving hands-on scientists real solutions rather than new layers of troubleshooting.
In addition to direct couplings, bromine’s presence means the compound will stand up to strong bases and acids better than many analogs. This stability has helped me avoid the heartbreak of “mystery peaks” in my LC/MS chromatograms. Reliability often trumps raw reactivity, and working with this intermediate means less stress about unwanted rearrangement or decomposition while optimizing new pathways.
Scientists get used to certain recurring specifications, especially around product models. High-performing 5-Bromoquinazolin-4-One often comes with HPLC purity at 98% or greater, and minimal moisture content—wariness about silica or other leftover contaminants pays off. Batch consistency always deserts from non-reputable sources, leaving ugly surprises for downstream applications.
True quality assurance does not stop at the technical sheet. Reliable lots show repeatable melting points, stable storage up to twelve months at ambient temperature away from light and moisture, and clear solubility in organic solvents like DMSO or DMF. Every time I ignored such cues out of haste, I paid with failed couplings or time-intensive re-purification. Complacency in specification checks often comes back to bite, so good practice demands scrutiny.
Even simple reactions sometimes get the best of us. Installing amines or alkyl groups onto the quinazoline core with this compound cuts unnecessary headaches. Whether running carbon-nitrogen or carbon-carbon bond-forming reactions, bromo-quinazolinone responds quickly to standard conditions, making it popular with both experienced and novice synthetic chemists.
What stands out is its resistance to harsh conditions. During a series of palladium-catalyzed coupling reactions, I challenged the bromo compound’s limits—base strength, temperature, and time. Rather than falling apart or yellowing, the mother liquor often remained clear, with only trace byproducts. Purification followed simple chromatographic techniques, with sharp peaks by HPLC or TLC showing up reliably. This ease of handling shortens development cycles and allows new ideas to move out of the proof-of-concept stage faster.
Another factor is waste generation. In a world where green chemistry is more than just a buzzword, using intermediates that react cleanly and produce minimal side-products counts for a lot. Time saved filtering sludge, disposing of hazardous halogen byproducts, or troubleshooting stubborn emulsions frees up energy for what really matters: designing new molecules.
I have seen plenty of batches that looked fine to the naked eye yet torpedoed a week’s work. Visual checks give clues, but unscheduled repeat reactions signal bigger issues lurking beneath. Substandard 5-Bromoquinazolin-4-One fails at predictable coupling yields, causes unexpected TLC patterns, and leads to yellow or brown streaks in product chromatography. Besides low yield, these subtle indicators set back research.
Adulteration or inconsistent synthesis processes often hide in “discounted” or “bulk” batches floating around the internet. In one instance, after comparing pure and cheap samples side by side, the subpar material dissolved unevenly and fouled glassware with fine particulates. This wasn’t just an inconvenience—it risked introducing metal impurities into downstream reactions, which proved nearly impossible to trace until days later. These hard lessons feed a healthy skepticism about cut-rate chemical sources.
There’s no shortage of halogenated quinazolinones to choose from. Some researchers still opt for chlorinated or iodinated quinazolinones because of lower cost or perceived higher reactivity. In mid-scale or industrial runs, these differences become more glaring. Chlorinated versions often require higher activation energy, needing extreme heat or aggressive catalysts, wasting both time and energy.
Iodinated analogs, while highly reactive, bring instability. Over my career, I learned that the extra cost and logistical complications tied to their storage and handling rarely pay off unless nothing else works. Bromo-quinazolinones, in contrast, bring just enough punch without the drama, and the chemistry rarely calls for specialized equipment—standard glassware and common reagents will handle most scenarios without pause.
Supply chain hiccups have hit the chemical industry the same as many others. Sourcing 5-Bromoquinazolin-4-One in the past few years required flexibility, with shipping delays and fluctuating costs. Ensuring a robust in-house stock of such intermediates takes careful supplier vetting and a willingness to pay for certainty. Skimping on due diligence leads to missed deadlines in grant projects and publication targets, a reality many in academia or industry know too well.
Not all issues revolve around the compound itself. Regulatory demands in several countries increased, limiting available overseas suppliers due to compliance burdens. Those in charge of procurement sometimes find themselves piecing together orders from several continents, relying on up-to-date inventory management and careful supplier relationships. I’ve learned to communicate openly with trusted vendors; building those relationships sometimes trumps the marginal savings promised by unproven distributors.
Moisture and light remain the big enemies. Over time, poorly stored bromo-quinazolinone absorbs ambient moisture, slowly yellowing and forming trace impurities detectable on finely tuned NMR or MS runs. While it does not explode or degrade into hazardous fragments under normal conditions, prudent storage—sealed glass containers in temperature-controlled dark cabinets—keeps the material in top form.
There are stories out there of warehouses with lax climate control letting valuable starting material degrade over the summer. In one case, a three-month-old batch opened to the air took on a faint musty smell and stubborn clumping. Once a powder loses its flow, it rarely regains usability. Whether in a government laboratory or a private research facility, neglecting these basics means waste and lost confidence in results.
Beyond technical performance, responsible scientists now look at lifecycle impact. 5-Bromoquinazolin-4-One, thanks to its reactivity and clean conversion, fits well into greener chemistry initiatives. The cleaner a step proceeds, the less downstream purification or environmental management a facility needs. Standardizing on reliable intermediates with track records of efficient transformations meets both budget and environmental goals.
Waste minimization isn’t simply a financial exercise. It also means fewer disposal headaches, less exposure risk for engineers or students, and better overall laboratory culture. Looking back, every successful synthesis campaign involving this intermediate resulted in less solvent waste, easier glassware cleaning, and less frustration among labmates wrestling with “smeary” plates or ghost peaks in mass spectra.
Organizational policies shape what gets bought and used. I have seen entire research teams turn projects around just by switching to higher-quality intermediates. Those using 5-Bromoquinazolin-4-One as a foundation saw faster hit-to-lead times, easier troubleshooting, and more productive combinatorial experiments.
Education around handling and procurement pays dividends. Lab supervisors encouraging careful documentation, supplier vetting, and ongoing quality checks find fewer interruptions to workflow. Novices gain confidence faster when every batch behaves predictably—a big deal in high-pressure, deadline-driven environments.
The pharmaceutical world keeps demanding new heterocycles with varied bioactivity. Bromo-substituted quinazolinones offer a canvas for the next wave of kinase inhibitors, antibiotics, and anti-cancer scaffolds. As computer-aided drug design advances, so too must the purity and reliability of starting materials. Newer generations of 5-Bromoquinazolin-4-One now enter the market supported by tighter quality control, trackable lot histories, and digital certificates of analysis. These aren’t simply paperwork—they represent hard-won trust between manufacturer and bench researcher.
Synthetic organic chemistry faces growing complexity from both targets and regulatory expectations. Integrating trustworthy intermediates like this compound, supported by rigorous analytics, reduces headaches and levels the field for smaller labs competing with well-funded giants.
Better outcomes come from proactive engagement within the scientific community. Advocating for third-party batch testing, supporting open data around purity, and direct dialogue with vendors will continue improving quality. Where resources allow, joint laboratories can participate in round-robin purity assessments, giving more transparency to end-users.
For academic labs and small companies, forming consortia to bulk purchase and independently vet intermediates like 5-Bromoquinazolin-4-One drags standards upward and counteracts the fragmented, sometimes opaque world of specialty reagents. This collaborative spirit means less time wasted chasing purity or consistency issues.
In my lab, rewarding suppliers that consistently exceed stated specs (rather than scraping by at the minimum) engenders a shared sense of mission. Over time, data sharing and open-to-feedback attitudes also spur manufacturers to update processes, sharpen analytics, and reinvest in robust supply chains.
Having seen fads come and go, the basics still matter. Quality, traceability, and performance make or break research goals. Work with products you can trust, engage in regular supplier vetting, and keep an open mind for improvements in workflow or sourcing. Every lot of 5-Bromoquinazolin-4-One that lives up to its promise pays back in time saved, results gained, and a more enjoyable research journey.
Train new chemists not just to accept technical data at face value, but also to develop their own nose for purity, standards, and the telltale signs of trouble in intermediates. A good eye and a skeptical mind will do more for discovery than the shiniest new equipment or the latest protocol from a journal article.
While some corners of the market still cut corners, informed, engaged chemists who demand clear, reproducible quality in intermediates push the bar higher for everyone. That’s how better, more innovative, and safer chemistry gets done—and why 5-Bromoquinazolin-4-One deserves close attention.