9-ETHYLCARBAZOLE-3-CARBOXALDEHYDE N-BENZYL-N-PHENYLHYDRAZONE CAS:75238-79-8
9-Ethylcarbazole-3-carboxaldehyde N-benzyl-N-phenylhydrazone finds several important applications in the fields of organic synthesis, medicinal chemistry, and materials science. One of the primary uses of this compound is in the synthesis of more complex organic molecules. The hydrazone moiety allows for various chemical transformations, enabling the generation of derivatives that may exhibit different biological activities or enhanced properties. Researchers employ this compound as a versatile intermediate in multi-step synthetic pathways, especially in the development of pharmaceuticals and agrochemicals. In medicinal chemistry, 9-ethylcarbazole-3-carboxaldehyde N-benzyl-N-phenylhydrazone has been studied for its potential pharmacological effects. Compounds containing the carbazole framework often display interesting biological activities, including anti-inflammatory, antimicrobial, and anticancer properties. Therefore, the hydrazone derivative may serve as a scaffold for developing new therapeutic agents targeting specific diseases. Ongoing research aims to investigate its efficacy against cancer cell lines and other pathological conditions, which could lead to novel treatment options. Moreover, the compound's ability to form coordination complexes with metal ions enhances its utility in materials science. These metal complexes can exhibit unique electronic, optical, or magnetic properties, making them suitable for applications in organic light-emitting diodes (OLEDs), sensors, and catalysis. The design of polymeric materials incorporating this hydrazone could also facilitate advancements in nanotechnology and advanced materials. Additionally, 9-ethylcarbazole-3-carboxaldehyde N-benzyl-N-phenylhydrazone serves as a valuable reagent in analytical chemistry for detecting and quantifying aldehydes and ketones. Its reactivity can be exploited in various assays and methods, contributing to the broader field of chemical analysis. In educational laboratories, this compound can be utilized to demonstrate hydrazone formation and related reaction mechanisms, providing students with hands-on experience in organic synthesis and characterization techniques. While 9-ethylcarbazole-3-carboxaldehyde N-benzyl-N-phenylhydrazone holds promise in many areas, it is essential to follow safety protocols while handling this compound due to potential hazards associated with hydrazones. Overall, its versatility makes it a significant compound in both research and applied sciences, paving the way for future discoveries and innovations.
Composition | C28H25N3 |
Assay | 99% |
Appearance | white powder |
CAS No. | 75238-79-8 |
Packing | Small and bulk |
Shelf Life | 2 years |
Storage | Store in cool and dry area |
Certification | ISO. |