N-Boc-3-formyl-5-indoleboronic acid pinacol ester

Unlock the versatile potential of N-Boc-3-formyl-5-indoleboronic acid pinacol ester, a highly specialized chemical compound that holds immense value for researchers and scientists across various disciplines. With its unique structural features and exceptional purity, this compound stands as a crucial building block in the realms of pharmaceutical development, organic synthesis, and material science innovation.

Unraveling the Compound's Essence

N-Boc-3-formyl-5-indoleboronic acid pinacol ester, identified by its CAS number 1025707-92-9, is a meticulously crafted Fluorinated Compound that boasts a purity of at least 95%. Its molecular formula, C20H26BNO5, and a molecular weight of 371.24 g/mol, endow it with a distinct chemical profile that enables a wide range of applications.
The compound's MDL number, MFCD07364063, serves as a unique identifier, allowing researchers to easily access detailed technical information and support resources. Its versatility is further enhanced by the presence of the N-Boc, formyl, and boronic acid pinacol ester functional groups, which open up diverse avenues for chemical transformations and targeted synthesis.

Unlocking Pharmaceutical Potential

In the realm of pharmaceutical research, N-Boc-3-formyl-5-indoleboronic acid pinacol ester shines as a valuable starting material and intermediate. Its unique structural features can be leveraged to synthesize a wide range of drug candidates, targeting various therapeutic areas such as oncology, neurology, and metabolic disorders. Researchers can harness the compound's reactivity and selectivity to develop innovative pharmaceuticals with enhanced efficacy and improved pharmacological profiles.

Advancing Organic Synthesis

Beyond the pharmaceutical realm, this versatile compound finds its place as a crucial reagent in organic synthesis. Chemists can utilize its boronic acid pinacol ester moiety to engage in a variety of cross-coupling reactions, enabling the construction of complex molecular architectures. The N-Boc and formyl groups further expand the compound's versatility, allowing for selective transformations and the incorporation of diverse functional groups.
The ability to fine-tune the properties of the resulting compounds through strategic modifications of N-Boc-3-formyl-5-indoleboronic acid pinacol ester opens up new avenues for the development of innovative materials, functional molecules, and advanced intermediates.

Exploring Material Science Frontiers

In the realm of material science, N-Boc-3-formyl-5-indoleboronic acid pinacol ester emerges as a valuable tool for researchers seeking to engineer novel materials with enhanced performance characteristics. Its unique structural features can be leveraged to create polymers, coatings, or composites with improved thermal stability, mechanical strength, or optical properties. By incorporating this compound into advanced material systems, scientists can push the boundaries of what's possible, unlocking new possibilities in fields such as optoelectronics, energy storage, and beyond.

Comprehensive Support and Resources

To fully harness the potential of N-Boc-3-formyl-5-indoleboronic acid pinacol ester, researchers can access a wealth of technical information and support resources. The product page provides detailed specifications, including purity, solubility, and handling guidelines, ensuring seamless integration into your research workflows.
Additionally, a comprehensive library of scientific literature, application notes, and safety data sheets is available to guide you through the compound's diverse applications and unlock new avenues for discovery. Engage with our team of experts to delve deeper into the technical details and explore the full scope of this versatile chemical compound.

• CAS Number: 1025707-92-9
• Name: N-Boc-3-formyl-5-indoleboronic acid pinacol ester
• Reference Number