(1H-Indol-3-yl)acetaldoxime CAS:2776-06-9
(1H-Indol-3-yl)acetaldoxime plays a crucial role in organic synthesis and medicinal chemistry for the development of bioactive molecules and pharmaceutical intermediates. Chemists leverage its unique structure to introduce functional diversity and explore new reaction pathways in complex molecule synthesis. By incorporating this compound into molecular designs, researchers can modulate biological activities, optimize chemical reactivity, and investigate structure-activity relationships, leading to the discovery of novel drug candidates and biologically active compounds with potential therapeutic applications. Furthermore, this compound finds utility in chemical biology as a versatile tool for probing biological processes and molecular interactions. Its ability to mimic natural substrates and bind to specific targets enables researchers to study enzyme mechanisms, receptor-ligand interactions, and signaling pathways. Chemists use (1H-Indol-3-yl)acetaldoxime as a molecular probe to elucidate biochemical pathways, validate drug targets, and discover new biomolecular functions, contributing to advancements in drug discovery and fundamental biological research. Moreover, (1H-Indol-3-yl)acetaldoxime contributes to academic research endeavors focused on exploring the reactivity of nitrogen-containing heterocycles and investigating the pharmacological potential of oxime derivatives. Its role as a versatile synthetic intermediate fosters investigations into chemical reactivity, molecular recognition processes, and structure-based drug design. By leveraging the synthetic capabilities of this compound, researchers continue to uncover new insights into organic chemistry, chemical biology, and drug development, driving innovation and progress in the field of chemical sciences.
Composition | C10H10N2O |
Assay | 99% |
Appearance | white powder |
CAS No. | 2776-06-9 |
Packing | Small and bulk |
Shelf Life | 2 years |
Storage | Store in cool and dry area |
Certification | ISO. |