Applications and Significance of (4-Bromophenyl)-(1H-indol-7-yl)methanone in Modern Chemistry
In the realm of advanced chemical synthesis, the strategic utilization of versatile intermediates is paramount. (4-Bromophenyl)-(1H-indol-7-yl)methanone, known by its CAS number 91714-50-0, is a compound that has garnered significant attention due to its broad applicability in pharmaceutical research and organic chemistry. As a manufacturer and supplier, understanding the intrinsic value and diverse applications of this molecule is key to serving the needs of the global market.
The primary significance of (4-Bromophenyl)-(1H-indol-7-yl)methanone lies in its role as a sophisticated building block for creating more complex molecular structures. The indole scaffold is a privileged structure in medicinal chemistry, found in numerous biologically active compounds. The appended bromophenyl ketone moiety provides excellent opportunities for further chemical modification. The bromine atom, for instance, is an ideal leaving group for palladium-catalyzed cross-coupling reactions, such as Suzuki, Stille, and Heck couplings, allowing for the introduction of various carbon-based substituents. This capability is fundamental in the synthesis of novel drug candidates and advanced materials.
Pharmaceutical companies often utilize this intermediate in the multi-step synthesis of Active Pharmaceutical Ingredients (APIs). Its structure can be elaborated to form compounds with potential therapeutic effects in areas such as oncology, neurodegenerative diseases, and infectious diseases. Researchers looking to buy (4-Bromophenyl)-(1H-indol-7-yl)methanone for their drug discovery pipelines value its reliability and consistent quality, typically at a purity of 97% or higher, to ensure predictable synthetic outcomes.
Beyond pharmaceuticals, this compound finds utility in materials science. The introduction of indole and aryl ketone functionalities can influence the electronic and optical properties of organic molecules, making them candidates for applications in organic electronics, such as OLEDs or organic photovoltaics. The ability to precisely engineer these properties through synthetic routes involving intermediates like CAS 91714-50-0 is driving innovation in these fields.
For manufacturers and suppliers, offering (4-Bromophenyl)-(1H-indol-7-yl)methanone means contributing to cutting-edge scientific research and development. By ensuring a stable supply of this high-quality intermediate, backed by competitive pricing and robust technical support, chemical companies can empower their clients to push the boundaries of what's possible in drug development and material innovation. The demand for such well-defined and versatile chemical building blocks continues to grow, underscoring the importance of compounds like (4-Bromophenyl)-(1H-indol-7-yl)methanone in modern chemistry.
Perspectives & Insights
Agile Reader One
“The appended bromophenyl ketone moiety provides excellent opportunities for further chemical modification.”
Logic Vision Labs
“The bromine atom, for instance, is an ideal leaving group for palladium-catalyzed cross-coupling reactions, such as Suzuki, Stille, and Heck couplings, allowing for the introduction of various carbon-based substituents.”
Molecule Origin 88
“This capability is fundamental in the synthesis of novel drug candidates and advanced materials.”