4-(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 4-position of the oxazole ring contributes to its chemical properties, including its potential as a chromophore, which can absorb light in the ultraviolet-visible spectrum. This compound typically exhibits a yellow to orange color due to the nitro group, which can also influence its reactivity and solubility in various solvents. It is often used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. The nitro group can participate in electrophilic substitution reactions, while the oxazole ring can engage in various chemical transformations, making it a versatile building block in synthetic chemistry. Additionally, its stability and reactivity can be influenced by the presence of substituents on the aromatic ring, which can modulate electronic properties and steric effects.

4-(4-Nitrophenyl)-1,3-oxazole

13382-61-1: 4-(1,3-Oxazole-4-Yl)Nitro-Benzene, 4-(1,3-Oxazol-4-Yl)Nitro-Benzene, Oznb, 4-(1,3-Oxazole-4-Yl)Nitro-Benzene(Oznb)

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CAS 13382-61-1: 4-(4-Nitrophenyl)-1,3-oxazole

4-(4-Nitrophenyl)oxazole

Ref: 3D-FN143996

4-(4-Nitrophenyl)oxazole

Ref: IN-DA008089

4-(4-Nitrophenyl)oxazole

Ref: 54-OR929279

4-(4-Nitrophenyl)oxazole

Ref: 10-F092021