2-Ethyl-5-(1H-indol-2-yl)-1,3,4-oxadiazole is a heterocyclic compound characterized by the presence of an oxadiazole ring fused with an indole moiety. This compound typically exhibits a range of interesting properties due to its unique structural features. The oxadiazole ring contributes to its potential as a bioactive molecule, often displaying properties such as fluorescence and photostability, which are valuable in various applications, including organic electronics and pharmaceuticals. The indole fragment is known for its biological significance, often associated with various pharmacological activities. Additionally, the ethyl substituent can influence the compound's solubility and reactivity. The compound may also exhibit specific interactions with biological targets, making it a subject of interest in medicinal chemistry. Its synthesis usually involves multi-step organic reactions, and it can be characterized using techniques such as NMR spectroscopy, mass spectrometry, and X-ray crystallography to confirm its structure and purity. Overall, 2-ethyl-5-(1H-indol-2-yl)-1,3,4-oxadiazole represents a versatile scaffold in chemical research.

2-ethyl-5-(1H-indol-2-yl)-1,3,4-oxadiazole

95446-30-3: 2-Ethyl-5-(1H-indol-2-yl)-1,3,4-oxadiazole is a heterocyclic compound characterized by the presence of an oxadiazole ring fused with an indole moiety. This compound typically exhibits a range of interesting properties due to its unique structural features. The oxadiazole ring contributes to its potential as a bioactive molecule, often displaying properties such as fluorescence and photostability, which are valuable in various applications, including organic electronics and pharmaceuticals. The indole fragment is known for its biological significance, often associated with various pharmacological activities. Additionally, the ethyl substituent can influence the compound's solubility and reactivity. The compound may also exhibit specific interactions with biological targets, making it a subject of interest in medicinal chemistry. Its synthesis usually involves multi-step organic reactions, and it can be characterized using techniques such as NMR spectroscopy, mass spectrometry, and X-ray crystallography to confirm its structure and purity. Overall, 2-ethyl-5-(1H-indol-2-yl)-1,3,4-oxadiazole represents a versatile scaffold in chemical research.

CAS 95446-30-3

2-ethyl-5-(1H-indol-2-yl)-1,3,4-oxadiazole

2-(5-ethyl-1,3,4-oxadiazol-2-yl)-1H-indole

Ref: 10-F495254