N-Cbz-3-piperidinylcarboxaldehyde is a chemical compound characterized by its piperidine ring structure, which is a six-membered ring containing one nitrogen atom. The "N-Cbz" designation indicates that the nitrogen atom is protected by a carbobenzyloxy (Cbz) group, which enhances the compound's stability and solubility. The presence of the aldehyde functional group (-CHO) at the 3-position of the piperidine ring is significant, as it contributes to the compound's reactivity and potential applications in organic synthesis. This compound is typically used in the synthesis of various pharmaceuticals and biologically active molecules due to its ability to participate in further chemical reactions, such as nucleophilic additions. Its properties, including solubility and reactivity, can be influenced by the presence of the Cbz protecting group, making it a versatile intermediate in synthetic chemistry. As with many organic compounds, handling should be done with care, following appropriate safety protocols to mitigate any potential hazards.

N-Cbz-3-piperidinylcarboxaldehyde

201478-72-0: Benzyl 3-Formylpiperidine-1-Carboxylate

3-Formyl-piperidine-1-carboxylic acid benzyl ester

Piperidine-3-carboxaldehyde, N-CBZ protected

3-Formyl-piperidine-1-carboxylic acid benzyl ester is a reductive agent that can be used to prepare indole derivatives from the corresponding hydrazines. This product can be obtained as an off-white solid in high yields, and it is stable under acidic conditions.

CAS 201478-72-0: N-Cbz-3-piperidinylcarboxaldehyde

3-Formyl-piperidine-1-carboxylic acid benzyl ester

Ref: 10-F087355

Piperidine-3-carboxaldehyde, N-CBZ protected

Ref: 54-OR1094

3-Formyl-piperidine-1-carboxylic acid benzyl ester

Ref: 3D-FF56377

1-Piperidinecarboxylic acid, 3-formyl-, phenylmethyl ester

Ref: IN-DA002DFZ