1-Cbz-4-Piperidone

1-Cbz-4-Piperidone Suppliers list

Properties, preparation and application of 1-cbz-4-piperidone
1-cbz-4-piperidone plays an important role in many fields. For example, in the field of medicine, it is often used to reduce p....
Jul 29，2022

1-Cbz-4-Piperidone Basic information

Product Name:	1-Cbz-4-Piperidone
Synonyms:	1-(BENZYLOXYCARBONYL)-4-PIPERIDINONE;1-CARBOBENZOXY-4-PIPERIDONE;1-N-CBZ-4-PIPERIDONE;PIPERIDIN-4-ONE, CBZ PROTECTED;N-CBZ-4-PIPERIDONE;N-BENZYLOXYCARBONYLPIPERIDIN-4-ONE;N-BENZYLOXYCARBONYLPIPERIDONE;1-PIPERIDINECARBOXYLICACID,4-OXO-,PHENYLMETHYLESTER
CAS:	19099-93-5
MF:	C13H15NO3
MW:	233.26
EINECS:	606-227-7
Product Categories:	Piperidine Series;Building Blocks;Chemical Synthesis;Heterocyclic Building Blocks;Piperidones;Piperidines;Aromatics;Heterocycles;Pyrans, Piperidines & Piperazines;Pyrans, Piperidines &Piperazines;API intermediates;Miscellaneous Biochemicals;19099-93-5
Mol File:	19099-93-5.mol

1-Cbz-4-Piperidone Chemical Properties

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
pka	-1.63±0.20(Predicted)
form	Solid or Lliquid
Specific Gravity	1.185
color	White to pale yellow
BRN	1533716
InChI	InChI=1S/C13H15NO3/c15-12-6-8-14(9-7-12)13(16)17-10-11-4-2-1-3-5-11/h1-5H,6-10H2
InChIKey	VZOVOHRDLOYBJX-UHFFFAOYSA-N
SMILES	N1(C(OCC2=CC=CC=C2)=O)CCC(=O)CC1
CAS DataBase Reference	19099-93-5(CAS DataBase Reference)

Safety Information

Hazard Codes	Xi
Risk Statements	36/37/38
Safety Statements	23-24/25-36-26-37/39
WGK Germany	3
HS Code	29333990
Storage Class	10 - Combustible liquids
Hazard Classifications	Acute Tox. 4 Oral Aquatic Chronic 3

MSDS Information

Provider	Language
SigmaAldrich	English
ALFA	English

1-Cbz-4-Piperidone Usage And Synthesis

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-Cbz-4-Piperidone is the starting material in biheteroaromatic diphosphine oxides-catalyzed stereoselective direct aldol condensation reactions.

1-Cbz-4-Piperidone Preparation Products And Raw materials

Raw materials

Preparation Products

Tag:1-Cbz-4-Piperidone(19099-93-5) Related Product Information

1-[(Benzyloxy)carbonyl]piperidine-4-carboxylic acid Benzyl benzoate 4-Piperidinone N-Carbobenzyloxyglycine 2-Piperidone N-Carbethoxy-4-piperidone 4,4-Piperidinediol hydrochloride tert-Butyl carbazate Thalidomide DROPERIDOL Benzyl alcohol Haloperidol Benzyl bromide Trimethoprim Ethyl N- Cbz -piperidine-4-carboxylate 4-Carboxymethoxy-piperidine-1-carboxylic acid benzyl ester Diphenoxylate 1-Cbz-2-phenyl-piperidin-4-one

Related articles