Discover the versatility of N-Cyclopropylthiophene-3-carboxamide, a premium Building Block compound with a CAS number of 1090897-27-0. This high-purity (98%) thiophene derivative boasts a molecular weight of 167.23g/mol, offering a unique blend of reactivity and stability. Crafted with precision, it serves as a valuable precursor in diverse chemical applications, from pharmaceuticals to agrochemicals. Handle with care, as it may cause skin and eye irritation. Store in a cool, well-ventilated area to ensure long-term performance. Elevate your research and synthesis with this exceptional Building Block, unlocking new possibilities in your laboratory.
Unlock the versatile potential of N-Cyclopropylthiophene-3-carboxamide, 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 Thiophenes-based building block is poised to become an indispensable tool in the hands of innovative researchers and chemists.
At the heart of this compound lies a captivating fusion of a cyclopropyl group and a thiophene ring, adorned with a carboxamide functionality. This intricate design, identified by the CAS number 1090897-27-0, endows N-Cyclopropylthiophene-3-carboxamide with a distinct chemical profile that sets it apart as a valuable asset in a wide range of applications.
In the realm of pharmaceutical research, N-Cyclopropylthiophene-3-carboxamide shines as a versatile building block. Its unique structural features allow for the synthesis of innovative drug candidates, targeting a diverse array of therapeutic areas. Researchers can harness the compound's reactivity and selectivity to develop novel compounds with enhanced pharmacological properties, paving the way for groundbreaking advancements in the treatment of various health conditions.
The cyclopropyl moiety, known for its distinctive electronic and steric properties, can be strategically incorporated into pharmaceutical molecules, leading to improved bioavailability, metabolic stability, and target specificity. Meanwhile, the thiophene ring and carboxamide functionality offer additional opportunities for further functionalization and optimization, unlocking new possibilities in the quest for more effective and safer therapeutic solutions.
Beyond the pharmaceutical realm, N-Cyclopropylthiophene-3-carboxamide also finds its place in the dynamic world of agrochemicals. Its chemical structure and inherent properties make it a valuable precursor in the development of advanced crop protection agents. By leveraging the unique characteristics of this compound, researchers can formulate potent and selective pesticides, herbicides, or fungicides that safeguard crops while minimizing environmental impact.
The cyclopropyl group, with its distinct electronic distribution and steric effects, can contribute to the enhanced efficacy and selectivity of agrochemical compounds. When combined with the thiophene and carboxamide moieties, N-Cyclopropylthiophene-3-carboxamide becomes a versatile platform for the synthesis of novel agrochemical products that address the evolving challenges faced by modern agriculture.
Beyond its pharmaceutical and agrochemical applications, N-Cyclopropylthiophene-3-carboxamide shines as a valuable tool in the realm of general chemical synthesis. Its unique structural features and inherent reactivity make it a sought-after building block for the creation of a wide range of novel compounds and materials.
Chemists and material scientists can harness the versatility of N-Cyclopropylthiophene-3-carboxamide to explore new frontiers in organic synthesis, polymer chemistry, and material science. The compound's ability to participate in a variety of chemical transformations, such as cycloadditions, substitutions, and coupling reactions, opens up a world of possibilities for the development of innovative products with tailored properties and functionalities.