| Identification | More | [Name]
1-Cbz-4-Piperidone | [CAS]
19099-93-5 | [Synonyms]
1-(BENZYLOXYCARBONYL)-4-PIPERIDINONE
1-CARBOBENZOXY-4-PIPERIDONE
1-N-CBZ-4-PIPERIDONE
1-Z-4-PIPERIDONE
4-OXO-PIPERIDINE-1-CARBOXYLIC ACID BENZYL ESTER
BENZYL 4-OXO-1-PIPERIDINECARBOXYLATE
BENZYL 4-OXOPIPERAZINE-1-CARBOXYLATE
N-BENZYLOXYCARBONYL-4-PIPERIDONE
N-BENZYLOXYCARBONYLPIPERIDIN-4-ONE
N-BENZYLOXYCARBONYLPIPERIDONE
N-CBZ-4-PIPERIDONE
PIPERIDIN-4-ONE, CBZ PROTECTED
BENZYL 4-OXO-1-PIPERIDINECARBOXYLATE, 99 %
Benzyl 4-oxo-1-piperazinecarboxylate
N-Benzyloxycarbonyl-4-Pipridone
N-Benzyloxycarbonyl-4-piperidone, 98+%
BENZYL 4-OXOPIPERIDINE-1-CARBOXYLATE
1-CBZ-4-PIPERIDONE
N-Benzyloxycarbonyl-4-piperido
Cbz-4-piperidone | [EINECS(EC#)]
606-227-7 | [Molecular Formula]
C13H15NO3 | [MDL Number]
MFCD00673144 | [Molecular Weight]
233.26 | [MOL File]
19099-93-5.mol |
| Chemical Properties | Back Directory | [Appearance]
Colourless Oil | [Melting point ]
38-41°C | [Boiling point ]
114-140 °C/0.25 mmHg (lit.) | [density ]
1.172 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.542(lit.)
| [Fp ]
>110 °C | [storage temp. ]
Sealed in dry,2-8°C | [solubility ]
Chloroform, Dichloromethane, Ethyl Acetate, Methanol | [form ]
Solid or Lliquid | [pka]
-1.63±0.20(Predicted) | [color ]
White to pale yellow or clear | [Specific Gravity]
1.185 | [BRN ]
1533716 | [InChIKey]
VZOVOHRDLOYBJX-UHFFFAOYSA-N | [CAS DataBase Reference]
19099-93-5(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) .
S24/25:Avoid contact with skin and eyes .
S36:Wear suitable protective clothing .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [WGK Germany ]
3
| [HS Code ]
29333990 |
| Hazard Information | Back Directory | [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.3 | [General Description]
1-Z-4-Piperidone is the starting material in biheteroaromatic diphosphine oxides-catalyzed stereoselective direct aldol condensation reactions. |
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