3-(3-Methyl-1,2,4-oxadiazol-5-yl)benzaldehyde is an organic compound characterized by its unique structure, which includes a benzaldehyde moiety and a 1,2,4-oxadiazole ring. The presence of the oxadiazole ring imparts specific chemical properties, such as potential reactivity and stability under various conditions. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents like ethanol and dimethyl sulfoxide (DMSO), but may have limited solubility in water. Its molecular structure allows for various applications in fields such as medicinal chemistry, where it may serve as a building block for synthesizing biologically active compounds. The compound's reactivity can be influenced by the aldehyde functional group, which is known for its ability to participate in nucleophilic addition reactions. Additionally, the presence of the methyl group on the oxadiazole ring can affect the electronic properties and steric hindrance, potentially influencing its biological activity and interactions with other molecules. Overall, 3-(3-methyl-1,2,4-oxadiazol-5-yl)benzaldehyde is a versatile compound with significant potential in research and development.

3-(3-methyl-1,2,4-oxadiazol-5-yl)benzaldehyde

273727-50-7: 3-(3-Methyl-1,2,4-oxadiazol-5-yl)benzaldehyde is an organic compound characterized by its unique structure, which includes a benzaldehyde moiety and a 1,2,4-oxadiazole ring. The presence of the oxadiazole ring imparts specific chemical properties, such as potential reactivity and stability under various conditions. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents like ethanol and dimethyl sulfoxide (DMSO), but may have limited solubility in water. Its molecular structure allows for various applications in fields such as medicinal chemistry, where it may serve as a building block for synthesizing biologically active compounds. The compound's reactivity can be influenced by the aldehyde functional group, which is known for its ability to participate in nucleophilic addition reactions. Additionally, the presence of the methyl group on the oxadiazole ring can affect the electronic properties and steric hindrance, potentially influencing its biological activity and interactions with other molecules. Overall, 3-(3-methyl-1,2,4-oxadiazol-5-yl)benzaldehyde is a versatile compound with significant potential in research and development.

3-(3-Methyl-1,2,4-oxadiazol-5-yl)benzaldehyde

CAS 273727-50-7

3-(3-methyl-1,2,4-oxadiazol-5-yl)benzaldehyde

3-(3-Methyl-1,2,4-oxadiazol-5-yl)benzaldehyde

Ref: 54-OR14886