5-(4-Nitrophenyl)-1,3-oxazole is an organic compound characterized by its oxazole ring, which is a five-membered heterocyclic structure containing both nitrogen and oxygen atoms. The presence of a nitrophenyl group at the 5-position of the oxazole ring contributes to its chemical properties, including increased electron-withdrawing effects due to the nitro group. This compound typically exhibits a yellow crystalline appearance and is soluble in organic solvents. It is often utilized in organic synthesis and as an intermediate in the production of various pharmaceuticals and agrochemicals. The nitro group can participate in electrophilic aromatic substitution reactions, making the compound a versatile building block in synthetic chemistry. Additionally, 5-(4-nitrophenyl)-1,3-oxazole may exhibit biological activity, which can be of interest in medicinal chemistry. Safety data should be consulted for handling, as nitro compounds can be hazardous. Overall, this compound is significant in both industrial and research applications due to its unique structural features and reactivity.

5-(4-NITROPHENYL)-1,3-OXAZOLE

CAS 1014-23-9: 5-(4-NITROPHENYL)-1,3-OXAZOLE

5-(4-Nitrophenyl)oxazole

Ref: 54-OR1316

5-(4-Nitro-phenyl)-oxazole

Ref: 10-F317305

5-(4-Nitrophenyl)oxazole

Ref: 3D-BAA01423

Oxazole, 5-(4-nitrophenyl)-

Ref: IN-DA0004F1