Unlock the versatile potential of this premium Building Block, 1-(Toluene-4-sulfonyl)-1H-indole-3-boronic acid, pinacol ester. Crafted with exceptional precision, this compound boasts a CAS number of 1073354-51-4 and a molecular weight of 397.30g/mol. Its unique chemical structure, featuring a toluene-4-sulfonyl group and a boronic acid pinacol ester, makes it a valuable asset for your advanced research and synthesis projects. Handle with care, as it is classified as harmful and irritant, requiring proper personal protective equipment and storage in a cool, well-ventilated area. Elevate your experiments to new heights with the reliability and performance of this exceptional Building Block.
Unlock the versatile potential of 1-(Toluene-4-sulfonyl)-1H-indole-3-boronic acid, pinacol ester, a meticulously crafted 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 Ester derivative is poised to become an indispensable tool in the hands of researchers and innovators across various industries.
This captivating compound, identified by its CAS number 1073354-51-4, is a solid substance with a molecular weight of 397.30g/mol. Its chemical formula, C20H24BNO3S, and MDL number MFCD08063118 provide a distinct identity, allowing researchers to easily track and reference this versatile building block.
The true power of 1-(Toluene-4-sulfonyl)-1H-indole-3-boronic acid, pinacol ester lies in its diverse applications, each one a testament to the compound's exceptional versatility.
Pharmaceutical Research: This compound serves as a crucial starting material in the synthesis of innovative pharmaceutical compounds. Its unique structural features enable the development of targeted therapies, addressing a wide range of health conditions and improving patient outcomes.
Agrochemical Innovation: In the realm of agrochemicals, this boronic acid ester contributes to the creation of advanced crop protection agents. Its distinct properties can be leveraged to formulate potent and selective pesticides, promoting healthier crops and higher yields while minimizing environmental impact.
Chemical Synthesis: As a versatile building block, 1-(Toluene-4-sulfonyl)-1H-indole-3-boronic acid, pinacol ester finds application in the synthesis of novel compounds with tailored properties. Its reactivity and selectivity make it a valuable reagent, enabling researchers to explore uncharted territories in materials science, organic chemistry, and beyond.
While this compound is classified as Harmful/Irritant, with associated hazard statements H302+H312+H332, H315, H319, and H335, proper handling and storage protocols can mitigate the risks. Wear protective equipment, work in a well-ventilated area, and follow the recommended P-statements to ensure a safe working environment. For long-term storage, keep the compound in a cool, dry place, away from direct light and moisture, to maintain its exceptional purity and stability.
To fully harness the potential of 1-(Toluene-4-sulfonyl)-1H-indole-3-boronic acid, pinacol ester, consult the comprehensive resources available, including technical data sheets, safety information, and relevant scientific literature. These materials will provide you with the necessary insights and guidance to optimize your research and development efforts, unlocking new possibilities in the realms of pharmaceuticals, agrochemicals, and beyond.