1-(Benzyloxycarbonyl)-4-piperidinone CAS 19099-93-5

Protective piperidone can be used for synthesis and transformation reactions that have attracted much attention, including Knoevenagel reaction, heterogeneous Diels-Alder reaction, and the formation of N-(4-piperidyl) hydroxyindole. The raw material for synthesis of GABA analogues by direct Barbier- type addition reaction of alkyl phosphonate.

N-Benzyloxycarbonyl-4-piperidone

1-benzyloxycarbonyl-piperidin-4-one

1-carbobenzyloxy-4-piperidone

1-Cbz-4-piperidinone

Benzyl 4-oxo-1-piperidinecarboxylate

1-Piperidinecarboxylic acid, 4-oxo-, phenylmethyl ester

1-(Benzyloxycarbonyl)-4-piperidinone

1-Z-4-Piperidone

4-Oxo-1-piperidinecarboxylic Acid Benzyl Ester

1-Cbz-4-piperidone

benzyl 4-oxopiperidine-1-carboxylate

1-Cbz-piperidin-4-one

1-Benzyloxycarbonyl-4-piperidine

N-CBZ-4-piperidone

1-Carbobenzoxy-4-piperidone

4-oxo-piperidine-1-carboxylic acid benzyl ester

MFCD00673144

Chemical Properties 
Colourless Oil

Uses 
Protected piperidinone that can undergo interesting synthetic transformations including the Knoevenagel reaction,1 hetero-Diels-Alder reactions,2 and reactions to form N-(4-piperidinyl)oxindoles.

General Description 
1-Z-4-Piperidone is the starting material in biheteroaromatic diphosphine oxides-catalyzed stereoselective direct aldol condensation reactions.