2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione

Unlock the versatile potential of 2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione, a highly specialized chemical compound that serves as a valuable building block in a wide range of scientific applications. With its unique molecular structure and exceptional purity, this Boron-containing compound opens up new avenues for researchers and chemists seeking to push the boundaries of innovation.

At the heart of this compound lies a tetramethyl-1,3,2-dioxaborolane moiety, strategically positioned on a phenyl ring and fused to a tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione scaffold. This intricate design grants the molecule a diverse array of chemical reactivity and potential applications, making it a versatile tool in the hands of skilled scientists.

Pharmaceutical Research and Development

In the realm of pharmaceutical research, 2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione shines as a valuable building block. Its boronic ester functionality allows for the synthesis of a wide range of pharmaceutical intermediates and active ingredients, enabling the development of innovative drug candidates targeting diverse therapeutic areas. Researchers can leverage the compound's unique properties to enhance the pharmacological profiles of their drug molecules, ultimately leading to more effective and safer treatments for patients.

The compound's versatility extends beyond pharmaceuticals, as it also finds applications in the agrochemical industry. Its boron-containing structure can be strategically incorporated into the design of advanced crop protection agents, contributing to the development of more potent and selective pesticides. This, in turn, helps to safeguard crops, improve yields, and promote sustainable agricultural practices.

Chemical Synthesis and Material Science

In the realm of chemical synthesis, 2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione serves as a valuable reagent and building block. Its boronic ester functionality can undergo a wide range of transformations, enabling the creation of novel compounds with tailored properties. Researchers in material science can leverage this compound to engineer advanced materials with enhanced characteristics, such as improved thermal stability, mechanical strength, or optical performance.

To ensure the highest quality and reliability, this compound is meticulously synthesized and purified, boasting a purity of 97% or higher. Its unique chemical identity, represented by the CAS number 'Not Available' and the MDL number 'MFCD22570339,' provides a clear identifier for researchers seeking specific information about the product.

Handling and Storage

While the hazard information for 2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione is still to be confirmed (TBC), it is essential to handle this compound with the utmost care and adhere to standard laboratory safety protocols. Appropriate personal protective equipment, such as gloves, goggles, and a well-ventilated work area, should be utilized when