4-(4-Nitrophenyl)piperidine, with the CAS number 26905-03-3, is an organic compound characterized by its piperidine ring substituted with a para-nitrophenyl group. This compound typically appears as a solid and is known for its pale yellow to light brown color. It possesses a molecular formula that reflects the presence of both nitrogen and oxygen in its structure, indicative of the nitro group. The presence of the nitro group contributes to its electron-withdrawing properties, which can influence its reactivity and interactions in various chemical environments. 4-(4-Nitrophenyl)piperidine is often utilized in organic synthesis and medicinal chemistry, serving as an intermediate in the production of pharmaceuticals and other biologically active compounds. Its solubility can vary depending on the solvent, and it may exhibit moderate to high stability under standard conditions. Safety precautions should be observed when handling this compound, as nitro-substituted compounds can be hazardous and may require specific storage and disposal methods.

4-(4-nitrophenyl)piperidine

26905-03-3: Piperidine, 4-(p-nitrophenyl)-, , 4-(4-Nitrophenyl)piperidine, Piperidine, 4-(4-nitrophenyl)-, , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 

4-(4-Nitro-Phenyl)-Piperidine (4NPP) is an asymmetric catalyst that has been used in the desymmetrization of diacylglycerols. This catalytic activity, along with its high specificity and high turnover number, makes 4NPP a promising candidate for use in industrial processes. 4NPP has also been shown to be a potent inhibitor of chiral amine oxidases and has been successfully used to inhibit the growth of resistant strains of bacteria.

CAS 26905-03-3: 4-(4-nitrophenyl)piperidine

4-(4-Nitro-Phenyl)-Piperidine

Ref: 3D-FN51536

4-(4-Nitrophenyl)piperidine

Ref: 54-OR15358

4-(4-NITRO-PHENYL)-PIPERIDINE

Ref: IN-DA00C1W3

4-(4-Nitro-phenyl)-piperidine

Ref: 10-F075573