Discover the versatility of 4-(1-Piperidylmethyl)phenylboronic acid, a premium Building Block compound with a unique molecular structure and a wide range of applications. Boasting a CAS number of 1200434-84-9 and a molecular weight of 219.09g/mol, this high-purity chemical offers exceptional performance and reliability in your laboratory creations. Crafted with precision, it presents a clear path to innovative synthesis, unlocking new possibilities in the realms of pharmaceuticals, agrochemicals, and beyond. Embrace the power of this exceptional compound and elevate your research to new heights, while exercising caution due to its potential hazardous nature.
Unlock the versatile potential of 4-(1-Piperidylmethyl)phenylboronic acid, a highly specialized chemical compound that holds the key to unlocking new frontiers in scientific research and development. With its unique molecular structure and exceptional purity, this Boronic Acid derivative is a valuable asset for researchers and chemists across various industries, from pharmaceuticals to material science.
4-(1-Piperidylmethyl)phenylboronic acid, identified by its CAS number 1200434-84-9, is a meticulously crafted chemical compound that combines the stability of a boronic acid moiety with the versatility of a piperidine-containing substituent. This strategic molecular design endows the compound with a diverse range of applications, making it a sought-after tool in the hands of innovative scientists and researchers.
In the realm of pharmaceutical research, 4-(1-Piperidylmethyl)phenylboronic acid serves as a crucial building block in the synthesis of novel drug candidates. Its unique chemical properties allow for the development of targeted therapies that address a wide spectrum of health conditions, from neurological disorders to metabolic diseases. Researchers can leverage the compound's reactivity and selectivity to create innovative pharmaceutical compounds with enhanced efficacy and improved pharmacological profiles.
The compound's versatility extends beyond the pharmaceutical domain, as it also finds applications in the agrochemical industry. Its distinct molecular structure contributes to the development of advanced crop protection agents, helping to safeguard crops and boost agricultural productivity while minimizing environmental impact.
In the field of material science, 4-(1-Piperidylmethyl)phenylboronic acid emerges as a valuable tool for researchers seeking to engineer novel materials with tailored properties. Its chemical composition and reactivity can be harnessed to create substances with enhanced mechanical strength, thermal stability, or optical characteristics, opening up new possibilities in areas such as advanced coatings, high-performance polymers, and functional materials.
This compound, with a molecular weight of 219.09g/mol, is classified under the MDL number MFCD06801706 and the HS code 2933399990. To ensure its optimal performance and maintain its high purity, 4-(1-Piperidylmethyl)phenylboronic acid should be stored in a cool, dry environment with proper ventilation, away from direct light and moisture.
While the specific hazard information is yet to be confirmed (TBC), it is essential to handle this compound with care, adhering to standard laboratory safety protocols. Appropriate personal protective equipment, such as gloves, goggles, and a face mask, should be used when working with this material.
Embrace the versatility of 4-(1-Piperidylmethyl)phenylboronic acid and unlock new possibilities in your research and development endeavors. Whether you're exploring innovative pharmaceutical solutions, advancing agrochemical technologies, or engineering cutting-edge materials, this compound can be the key to unlocking groundbreaking discoveries and transformative innovations. Consult the available resources, including technical data sheets and safety guidelines, to fully harness the potential of this remarkable chemical compound.