4-(5-Oxazolyl)benzaldehyde is an organic compound characterized by the presence of both an oxazole ring and a benzaldehyde functional group. The oxazole ring, a five-membered heterocycle containing nitrogen and oxygen, contributes to the compound's unique reactivity and potential biological activity. The benzaldehyde moiety provides an aldehyde functional group, which is known for its reactivity in various organic reactions, including condensation and oxidation processes. This compound typically appears as a crystalline solid and may exhibit moderate solubility in organic solvents. Its structure allows for potential applications in pharmaceuticals, agrochemicals, and as a building block in organic synthesis. The presence of the oxazole ring may impart specific properties such as antimicrobial or antifungal activity, making it of interest in medicinal chemistry. Additionally, the compound's reactivity can be exploited in the synthesis of more complex molecules, highlighting its utility in research and industrial applications. As with many organic compounds, safety precautions should be observed when handling 4-(5-Oxazolyl)benzaldehyde due to potential toxicity or reactivity.

4-(5-Oxazolyl)benzaldehyde

179057-31-9: 4-(5-Oxazolyl)benzaldehyde is an organic compound characterized by the presence of both an oxazole ring and a benzaldehyde functional group. The oxazole ring, a five-membered heterocycle containing nitrogen and oxygen, contributes to the compound's unique reactivity and potential biological activity. The benzaldehyde moiety provides an aldehyde functional group, which is known for its reactivity in various organic reactions, including condensation and oxidation processes. This compound typically appears as a crystalline solid and may exhibit moderate solubility in organic solvents. Its structure allows for potential applications in pharmaceuticals, agrochemicals, and as a building block in organic synthesis. The presence of the oxazole ring may impart specific properties such as antimicrobial or antifungal activity, making it of interest in medicinal chemistry. Additionally, the compound's reactivity can be exploited in the synthesis of more complex molecules, highlighting its utility in research and industrial applications. As with many organic compounds, safety precautions should be observed when handling 4-(5-Oxazolyl)benzaldehyde due to potential toxicity or reactivity.

CAS 179057-31-9

4-(5-Oxazolyl)benzaldehyde

4-(Oxazol-5-yl)benzaldehyde

Ref: IN-DA0026QI

4-(1,3-Oxazol-4-yl)benzaldehyde

Ref: 54-OR2128

4-(OXAZOL-5-YL)BENZALDEHYDE

Ref: 10-F534787

4-(1,3-Oxazol-5-yl)benzaldehyde

Ref: 3D-EHA05731