N-Benzyl-4-piperidone

N-Benzyl-4-piperidone Basic information
Product Name:N-Benzyl-4-piperidone
Synonyms:NSC 77933;1-BENZYL-4-PIPERIDINONE FOR SYNTHESIS;[(4-Oxopiperidin-1-yl)methyl]benzene, 1-Benzyl-4-oxopiperidine;N- benzylpiperidineketone;1-Benzyl-4-piperidone, 99%, 99%;N - benzyl - 4 - piperidine ketone (3612-20-2);N-BENZYL-4-PIPERIDONE;1-Benzylpiperidone
CAS:3612-20-2
MF:C12H15NO
MW:189.25
EINECS:222-782-4
Product Categories:Piperidines, Piperidones, Piperazines;pharmacetical;Phenyls & Phenyl-Het;Piperidine;Heterocyclic Compounds;Phenyls & Phenyl-Het;Amines;blocks;PHARMACEUTICAL INTERMEDIATES;Amines and Anilines;Carbonyl Compounds;Miscellaneous;Aromatics;ketone;Heterocycles;Isotope Labelled Compounds;3612-20-2
Mol File:3612-20-2.mol
N-Benzyl-4-piperidone Structure
N-Benzyl-4-piperidone Chemical Properties
Boiling point 134 °C7 mm Hg(lit.)
density 1.021 g/mL at 25 °C(lit.)
vapor pressure 0.079-0.15Pa at 20-25℃
refractive index n20/D 1.541(lit.)
Fp >230 °F
storage temp. 2-8°C
solubility 12g/l
pka7.07±0.20(Predicted)
form Oily Liquid
color Clear colorless to straw
Specific Gravity1.021
Water Solubility 12 g/L (20 ºC)
BRN 128556
LogP2.1 at 20℃ and pH9
CAS DataBase Reference3612-20-2(CAS DataBase Reference)
NIST Chemistry Reference4-Piperidinone, 1-(phenylmethyl)-(3612-20-2)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-43-22-20/21/22
Safety Statements 26-36-37/39
WGK Germany 3
Hazard Note Irritant
HS Code 29333999
MSDS Information
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1-(Phenylmethyl)-4-piperidinone English
SigmaAldrich English
ACROS English
ALFA English
N-Benzyl-4-piperidone Usage And Synthesis
Chemical PropertiesClear colorless to straw coloured oily liquid
UsesA substituted piperidine as pesticide
Uses1-Benzyl-4-piperidone is a pharmaceutical intermediate, it is used in penfluridol synthesis of bulk drugs.
Purification MethodsIf the physical properties show contamination, then dissolve it in the minimum volume of H2O, made strongly alkaline with aqueous KOH, extract it with toluene several times, dry the extract with K2CO3, filter, evaporate and distil the residue at high vacuum using a bath temperature of 160-190o, and redistil it. [Brookes & Walker J Chem Soc 3173 1957, Bolyard J Am Chem Soc 52 1030 1930.] The hydrochloride has m 159-161o (from Me2CO/Et2O), and the picrate has m 174-182o (from Me2CO/Et2O). [Grob & Brenneisen Helv Chim Acta 41 1184 1958, Beilstein 21/6 V 424.]
Benzoyl peroxide Ethyl 1-benzyl-4-oxo-3-piperidinecarboxylate hydrochloride N-BENZOYL-4-PIPERIDONE Benzyl chloride Benzyltriethylammonium chloride 9-Benzyl-9-azabicyclo[3.3.1]nonan-3-one Diphenoxylate Benzyl alcohol Triacetonamine 3-METHYL-5-METHOXYCARBONYL-1-BENZYL-4-PIPERIDONE HYDROCHLORIDE, 99 Benzyltrimethylammonium chloride METHYLPIPERIDONE 1-BENZYL-3-METHYL-4-PIPERIDONE 1-BENZYL-3,5-BIS(2-THIENYLMETHYLENE)TETRAHYDRO-4(1H)-PYRIDINONE Haloperidol 1-Benzyl-3-ethoxycarbonyl-4-piperidone 1-Benzylpiperazine N-Anisoyl-4-piperidone

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