4-Methoxyphenylboronic Acid
- CAS No.5720-07-0
- GradeIndustrial / Pharmaceutical
- Availability● In Stock
High-purity 4-Methoxyphenylboronic Acid (CAS 5720-07-0) designed for efficient Suzuki coupling reactions and pharmaceutical synthesis. Available in bulk quantities with certified COA.
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Product Overview
4-Methoxyphenylboronic Acid is a premier organic building block extensively utilized in modern synthetic chemistry. As a stable arylboronic acid derivative, this compound serves as a critical reagent for carbon-carbon bond formation, particularly within palladium-catalyzed cross-coupling protocols. Our manufacturing process ensures exceptional batch-to-batch consistency, making it an ideal choice for large-scale pharmaceutical intermediate production and advanced materials research.
We understand the demands of industrial synthesis, which is why our supply chain is optimized for reliability. Each production lot undergoes rigorous quality control testing to guarantee high purity levels suitable for sensitive catalytic reactions. Whether you are developing new active pharmaceutical ingredients or optimizing existing synthetic routes, this boronic acid provides the foundational reliability required for successful outcomes.
Technical Specifications
Quality assurance is paramount in chemical manufacturing. The following table outlines the key physical and chemical properties verified during our internal quality control processes. We maintain strict adherence to these specifications to support your regulatory compliance and process stability.
| Parameter | Specification |
|---|---|
| CAS Number | 5720-07-0 |
| Molecular Formula | C7H9BO3 |
| Molecular Weight | 151.96 g/mol |
| Appearance | White powder |
| Assay (Purity) | ≥99.0% |
| Water Content | ≤0.50% |
| Melting Point | 204-206 °C |
| Density | 1.17 g/cm3 |
Industrial Applications
The versatility of 4-Methoxyphenylboronic Acid makes it indispensable across multiple sectors of the fine chemical industry. Its primary application lies in Suzuki-Miyaura coupling reactions, where it acts as a nucleophilic partner to construct biaryl structures efficiently. This reaction type is a cornerstone in the synthesis of complex organic molecules, including liquid crystals, agrochemicals, and pharmaceutical intermediates.
Beyond standard coupling reactions, this compound is frequently employed in N-arylation processes. Research indicates its effectiveness in reactions catalyzed by copper-exchanged systems, facilitating the formation of carbon-nitrogen bonds essential for heterocyclic compound synthesis. Additionally, it serves as a valuable tool in academic and industrial research settings for investigating boron functionality in various chemical environments.
- Efficient reagent for Suzuki-Miyaura cross-coupling reactions.
- Key intermediate in the synthesis of pharmaceutical APIs.
- Utilized in N-arylation of imidazoles and amines.
- Stable profile suitable for long-term storage and transport.
- Compatible with various palladium and copper catalytic systems.
Storage and Packaging
To maintain optimal quality, proper storage conditions are essential. This product should be stored in a cool, dry, and well-ventilated area away from direct sunlight and moisture sources. Keeping the container tightly closed prevents hydration or oxidation, which could affect reactivity in sensitive catalytic processes. We offer flexible packaging solutions to meet diverse logistical needs, typically supplying in 25kg drums. Custom packaging configurations are available upon request to align with your specific production line requirements. Our global logistics network ensures timely delivery while maintaining product integrity throughout transit.
