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HS Code |
977472 |
| Product Name | 3-Formyl-4-Methoxyphenylboronic Acid |
| Cas Number | 881674-56-4 |
| Molecular Formula | C8H9BO4 |
| Molecular Weight | 179.97 g/mol |
| Appearance | Off-white to pale yellow solid |
| Melting Point | 157-161°C |
| Purity | Typically ≥ 97% |
| Solubility | Slightly soluble in water, soluble in DMSO and methanol |
| Smiles | COC1=CC(=CC(=C1)B(O)O)C=O |
| Storage Conditions | Store at 2-8°C, protect from moisture |
| Mdl Number | MFCD09969765 |
| Synonyms | 3-Formyl-4-methoxybenzeneboronic acid |
As an accredited 3-Formyl-4-Methoxyphenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 5 grams of 3-Formyl-4-Methoxyphenylboronic Acid, with tamper-evident sealed cap and product label. |
| Shipping | 3-Formyl-4-Methoxyphenylboronic Acid is shipped in tightly sealed containers to prevent moisture and contamination. The package is clearly labeled as a chemical, with appropriate hazard labeling if needed. Shipping complies with all relevant regulations for chemical transport, ensuring safe handling and timely delivery. Temperature control may be applied if required. |
| Storage | **Storage for 3-Formyl-4-Methoxyphenylboronic Acid:** Store in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and moisture. Keep container tightly closed when not in use. Protect from air and incompatible substances such as oxidizing agents. Recommended storage temperature is 2-8°C (refrigerated). Use appropriate personal protective equipment when handling. |
Applications of 3-Formyl-4-Methoxyphenylboronic Acid in Industrial ManufacturingAs a specialized manufacturer, we supply 3-Formyl-4-Methoxyphenylboronic Acid to multiple advanced segments of the fine chemicals and pharmaceutical industries. This key boronic acid derivative enables precise functionalization steps in complex molecular synthesis, supporting innovation and quality in targeted fields. Below, we detail specific industrial application scenarios reflecting actual market demand and current best practices for safe, compliant, and scalable integration within downstream production workflows. 1. Active Pharmaceutical Ingredient (API) Synthesis – Anticancer Small MoleculesThis material plays an essential role in Suzuki–Miyaura cross-coupling protocols for building structurally complex aromatic frameworks required in the synthesis of novel kinase inhibitors and targeted anticancer APIs. End users in pharma employ it as a boron source for the late-stage introduction of functionalized aryl groups, which often determine binding affinity and selectivity. Its controlled reactivity allows for step-economical assembly of drug scaffolds under mild conditions, improving yield while lowering impurity profiles in regulatory submissions. Industry compliance standards
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2. Agrochemical Intermediate Manufacturing – Crop Protectant SynthesisIn the agrochemical sector, processors depend on this boronic acid to construct aryl ether moieties and introduce aldehyde groups into active scaffolds required for herbicide and fungicide molecules. Its functionally rich profile supports selectivity enhancement and environmental fate modification in the final active ingredient, while scalable process compatibility allows integration into continuous manufacturing setups typical for this segment. Industry compliance standards
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3. Pharmaceutical Research – PROTAC (Proteolysis Targeting Chimera) Scaffold ConstructionRecent advances in targeted protein degradation have highlighted this building block as a core arylboronic acid for assembling bifunctional PROTAC molecules. Medicinal chemists utilize its distinct substitution pattern for linker chemistry, aiding solubility and conjugation to ligands that engage E3 ligases. The moderate electron-donating methoxy and reactive formyl site provide balanced reactivity, facilitating precise attachment and expanded PROTAC library development in early research and discovery settings. Industry compliance standards
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4. Specialty Materials – Electronic Chemical Synthesis for OLED IntermediatesThe specialty electronics sector relies on this phenylboronic acid for constructing methoxy- and formyl-functionalized aromatic layers used in organic light-emitting diode (OLED) display panel materials. Its precise electronic characteristics enable custom tuning of hole transport and light emission properties, especially in multi-layer device structures where defect minimization and batch-to-batch consistency are essential for manufacturing premium electronics with long operational lifespans. Industry compliance standards
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Working with chemicals daily in a controlled facility changes the way we view our products. 3-Formyl-4-methoxyphenylboronic acid stands out for its versatility in complex organic synthesis, particularly in our boronic acid lineup. As a chemical manufacturer, we commit to not only ensuring the right molecular structure—C8H9BO4, typically appearing in a fine, off-white powder—but also to understanding how our customers will use this compound downstream.
Most customers using this product are pursuing Suzuki-Miyaura cross-coupling reactions, often synthesizing bioactive molecules, advanced pharmaceutical intermediates, or specialty materials. Consistency in purity is vital. The specifications we follow in-house reflect lessons learned over years: product leaving our plant must meet a minimum purity of 97%, confirmed through both HPLC and NMR. There’s a difference when the person signing off the batch knows a missed impurity could compromise entire research timelines or manufacturing cycles.
Among the boronic acids we prepare, 3-formyl-4-methoxyphenylboronic acid brings a valuable combination of functional groups. The formyl group at the third position acts as a reliable handle for further modification, and the methoxy substituent at the fourth position tunes the molecule’s electronic properties. We’ve watched researchers in medicinal chemistry fine-tune their syntheses by leveraging this specific arrangement, often chasing the right substitution pattern for a target drug scaffold.
By handling both gram-scale development batches and multi-kilogram production lots, we’ve had opportunities to witness the subtle yet significant differences this compound brings. Other boronic acids, lacking that methoxy or formyl group, fail to deliver key reactivity in certain settings. Our clients report success when making analogs that need the electron-donating and electron-withdrawing balance that comes from having both a methoxy and an aldehyde group on the aromatic ring.
With so many intermediates on the market, the temptation to judge by technical data sheets alone runs high. From our perspective, the real measure of quality is how product performs in the lab and pilot plant. Over the years, we’ve improved our purification methods, scaling up as we listened to feedback where mild yellow hues or trace metal contamination impacted high-sensitivity reactions.
Reliable synthesis protocols help, but impurities form subtly, especially with boronic acids prone to self-condensation. Our team developed a proprietary crystallization step, which we run at a specific temperature window, narrowing down the impurity profile below detection thresholds. Occasionally, we’ve had requests for bespoke particle sizes or alternative solvents for improved wetting in automated reactors; accommodating those requests builds trust and makes us rethink even basic assumptions about material handling.
You can’t overstate the impact of substituent effects on reaction efficiency. Experienced chemists who request 3-formyl-4-methoxyphenylboronic acid know this compound increases yield and selectivity in Suzuki couplings where steric and electronic effects must be carefully balanced. Other suppliers often push more generic options, but we’ve seen how an alteration at either the methoxy or formyl position leads to dramatic shifts in reaction profiles or crystal morphology downstream.
In our facility, analytical teams work side by side with process chemists. We document each lot’s reaction behavior in pilot test runs, giving us an archive of real results. In the pharmaceutical industry, where a single synthetic step can determine overall yield and cost structure, there’s little room for unpredictability. Our feedback loop includes not only our synthetic runs but also direct customer communication, which often highlights problems with other boronic acids—mainly low solubility, inconsistent particle size, or higher pinacol formation.
Not every chemical company pays attention to what actually happens after shipping. In practice, many early pharma screens require the rapid assembly of various aromatic rings via palladium-catalyzed transformations. 3-Formyl-4-methoxyphenylboronic acid plays a key role, specifically when the end product demands a substitution at the para and meta positions for bioactivity.
We keep direct lines with discovery scientists, who explain how a seemingly minor impurity or variation in polymorph can derail full-scale manufacturing. With new molecular designs, stable handling and reliable solubility in both polar and non-polar media count for more than just numbers—quality translates to less troubleshooting and faster development cycles.
Through hands-on manufacturing, the differences among structurally related boronic acids become obvious. Boronic acid groups at ortho or meta positions lack the same utility in many cross-coupling scenarios. Market data and customer conversations confirm that analogous compounds, such as 4-methoxyphenylboronic acid or 3-formylphenylboronic acid, rarely match the performance profile needed when both the formyl and methoxy groups are present.
We’ve processed various isomers and noted differences in melting point, rate of cross-coupling, and hydroscopic character. The dual functionality on this compound introduces a balance between reactivity and processability, impacting yield in key steps—especially in large-scale runs where solvent choices and temperature control come sharply into play.
Sourcing 3-formyl-4-methoxyphenylboronic acid from a manufacturer ensures traceability and immediate mitigation for lot-to-lot variability. We offer both batch and continuous process capabilities, having invested in real-time analytic equipment for tighter control, which means flagged deviations never reach the customer. Collaborative troubleshooting has led us to tweak our filtration and drying steps, maintaining consistently low water content, an area that often causes headaches when other sources deliver material with elevated moisture.
We keep detailed histories on every batch, tracking raw material sources, impurity trends, and post-shipment feedback. Many end-users undersell the value of this traceability until their process throws an unexplained error. Allowing rapid look-back and root cause analysis, we guide customers through trouble-shooting that would slow down a project if less care was taken on the manufacturing floor.
With global demand for new pharmaceuticals and advanced materials rising, production of specialized boronic acids is no longer a side business; it’s a central capability. 3-Formyl-4-methoxyphenylboronic acid helps push forward molecular design, often serving as a stepping stone for the formation of C-C and C-N bonds crucial to modern active pharmaceutical ingredients and electronic materials.
Teams inside our plant have been called on to run custom syntheses and adapt conditions in response to ever-tighter specifications, such as prepping water-free product for air-sensitive syntheses or fitting particle size ranges for use in flow chemistry. This flexibility only comes from running the reactions yourself, day in and out, seeing firsthand which parameters shift batch outcome.
Our product development has never been static. Years ago, production chemists flagged unnecessary side reactions complicating isolation after the boronation stage. Internal R&D focused on optimizing base and solvent selection, leading to improved throughput and smoother crystallization. The current material we send out reflects layers of process improvement and customer-driven feedback.
One research client highlighted batch-to-batch inconsistency in melting point when sourcing from another manufacturer. By tracking impurities via LC-MS, we found trace halides tied to particular lots of boronic acid catalyst. By switching to a higher-purity input lot and extending the recrystallization phase, we resolved the issue and delivered a tighter melting point range. Quality backed by data and internal troubleshooting experience marks a significant advantage when shipping this product globally.
Production of boronic acids, especially those with sensitive substituents, requires respect for process safety and personal health. Our plant layout, ventilation, and workflows reflect years of hands-on safety engineering, from dust control at the micronization step to keeping cross-contamination below critical levels in shared equipment.
Team members learn on the floor which materials require more careful handling and which operations need extra monitoring. We reinforce regular training, not as a box-checking exercise, but because a prevented near-miss can save untold cost, downtime, or worse. Accidents in handling reactive boronic acids often stem from unchecked assumptions and imprecise process discipline.
We hold regular reviews after every batch cycle, looking at near-miss data, air monitoring results, and historical deviation logs. The culture supports open communication, allowing operators, chemists, and quality specialists to speak up about any concerns. New equipment or changes in production layout get evaluated with experienced staff input, since those running the process daily catch practical risks faster than any outside auditor.
As supply chains tighten and regulatory oversight rises, traceability back to the original manufacturer has become crucial. We guarantee full chain-of-custody records, from raw material selection to end-product release, verified with third-party testing where needed. This gives our partners clarity—no mystery intermediaries, no relabeling, no compromised origin story.
We maintain open lines with raw materials suppliers, avoiding last-minute substitutions that might introduce heavy metals or untested process aids. Our specification sheets offer more than minimum compliance information: they reflect tested batch data, historical impurity trends, and solvent residuals, shaped by direct customer requirements.
Long-term partners have noted supply crises where other sources dried up or shifted to off-standard material. By running our own synthesis lines and holding buffer inventory when needed, we absorb shocks in demand and provide reliability rare among trading houses. Frequent communication with our logistics teams, as well as backup routes and packaging options, demonstrates the value of building robust, transparent systems around a specialized chemical.
Chemical manufacturing thrives on close collaboration. We offer more than just product; many projects start with a lab notebook sketch or a call from a pharma chemist unsure which boronic acid variant supports their target structure. Since we control both process and scheduling, we deliver adjusted parameters—particle size, solvent-free options, custom pack-out, or even alternative salt forms—often on short notice.
Our plant technical team runs pilot batches before full-scale roll-out, allowing validation in real conditions. Clients see test samples derived straight from those pilot runs, not from old reserve stocks. This builds confidence for launch timelines and gives early warning about any scale-related shifts in impurity or physical form.
We approach each new request as a chance to map a better process, not just push existing inventory out the door. Having walked through countless changeovers and custom requests, our staff knows which bottlenecks slow production and what upsets stability—experience that lets us promise more than “standard grade” with real accountability behind every metric.
Sustainability isn’t just about regulatory compliance. On the floor, smart solvent selection, in-process recovery, and minimizing waste streams make daily differences. For boronic acids like this one, where multi-step syntheses generate solvent-rich effluents and spent reaction media, we invest in onsite distillation and catalyst reclamation instead of relying on downstream incineration.
Operators are trained to manage cleanup with minimized water use and to segregate hazardous fractions before downstream treatment. Aging equipment gets replaced with higher-efficiency alternatives, not for appearance but to cut real process losses and reduce emissions. These conscious decisions reflect the practical side of E-E-A-T principles: experience, expertise, authority, and trust all build from repeated, tangible commitment, not only words on a website or certificate in a file drawer.
As more industries integrate cross-coupling chemistry into their manufacturing toolkits, the need for high-quality, consistently produced boronic acids will only grow. 3-Formyl-4-methoxyphenylboronic acid, with its unique structure, is poised to play an increasing role both in research and in larger-scale finished product synthesis.
From the perspective of those who run the reactors and QC the shipments, every improvement, every closed feedback loop, and every direct client discussion matters. Experience on the floor—watching how humidity on hot days or a drift in reactor jacket temperatures translate to product properties—provides insights not taught in standard chemical engineering courses.
In the end, trust in a chemical manufacturer comes from more than a label or claims on a data sheet. It grows from repeated deliveries of real-world results, honest communication about limitations, and a drive to improve based on every batch that exits our doors. 3-Formyl-4-methoxyphenylboronic acid has become a benchmark product not by chance, but through years of listening, learning, and implementing changes that matter both to us as producers and to the chemists who rely on it every week.