Unlock the captivating potential of 1H-Indole-4-carboxaldehyde, a versatile building block with a rich molecular structure. This brown solid compound, boasting a purity of 97%, offers a molecular weight of 145.16g/mol and a melting point range of 139-145°C. Crafted with precision, it serves as a valuable precursor in diverse chemical applications, from pharmaceuticals to agrochemicals. Handle with care, as it is classified as harmful and irritant, requiring proper personal protective equipment and storage in a cool, well-ventilated area. Embrace the power of this exceptional indole derivative and elevate your research to new heights.
Unlock the captivating world of 1H-Indole-4-carboxaldehyde, a versatile and highly sought-after chemical compound that has captured the attention of researchers and scientists across diverse fields. With its unique molecular structure and exceptional purity, this Indole derivative offers a wealth of possibilities, from pharmaceutical breakthroughs to innovative material development.
At the heart of this compound lies a captivating indole core, adorned with a strategic aldehyde group at the 4-position. This strategic placement unlocks a realm of chemical reactivity, making 1H-Indole-4-carboxaldehyde a valuable building block in the synthesis of a wide range of compounds. Whether you're exploring new pharmaceutical frontiers or pushing the boundaries of material science, this versatile molecule is poised to be your key to unlocking groundbreaking discoveries.
In the dynamic world of pharmaceutical research, 1H-Indole-4-carboxaldehyde shines as a crucial starting material and intermediate. Its indole scaffold, combined with the reactive aldehyde functionality, allows for the creation of diverse drug candidates targeting a spectrum of health conditions. From neurological disorders to metabolic diseases, this compound's versatility empowers researchers to explore innovative therapeutic approaches, paving the way for life-changing breakthroughs.
Leveraging the inherent reactivity of the aldehyde group, chemists can seamlessly incorporate 1H-Indole-4-carboxaldehyde into complex molecular structures, unlocking new avenues for drug discovery. Its strategic placement within the indole framework enables the synthesis of a wide range of derivatives, each with the potential to exhibit unique pharmacological properties and therapeutic benefits.
Beyond the realm of pharmaceuticals, 1H-Indole-4-carboxaldehyde also finds its place in the dynamic world of agrochemicals. Its versatile nature allows for the development of advanced crop protection agents, contributing to the creation of a more sustainable and productive agricultural landscape.
The aldehyde functionality of this compound can be harnessed to synthesize novel pesticides, herbicides, and other agrochemical formulations. By strategically modifying the indole core and the aldehyde group, researchers can engineer highly targeted and effective agrochemicals that safeguard crops while minimizing environmental impact. This delicate balance between efficacy and eco-friendliness is the hallmark of 1H-Indole-4-carboxaldehyde's contribution to the agrochemical industry.
Beyond its pharmaceutical and agrochemical applications, 1H-Indole-4-carboxaldehyde also shines in the realm of material science. Its unique chemical structure and inherent reactivity make it a valuable precursor in the synthesis of advanced materials with tailored properties.
Researchers in the field of material science have recognized the potential of this compound to unlock new frontiers in areas such as polymer chemistry, coatings, and functional materials. By strategically incorporating 1H-Indole-4-carboxaldehyde into their formulations, scientists can create materials with enhanced thermal stability, improved mechanical strength, or even unique optical characteristics. These advancements pave the way for innovative applications in fields ranging from energy storage to aerospace engineering.
1H-Indole-4-carboxaldehyde, with its CAS number 1074-86-8, is a brown solid with a purity of 97%. Its molecular formula, C9H7NO, and a molecular weight of 145.16g/mol, make it a highly pure and well-defined compound. The compound's INCHI code, InChI=1S/C9H7NO/c11-6-7-2-1-3-9-8(7)4-5-10-9/h1-6,10H, and SMILES notation, O=Cc1cccc2[nH]ccc12,