1-Isobutyl-4-piperidone

  • CasNo:72544-16-2
  • purity:99%
Inquiry Add to cart

Details

Top quality factory supply 72544-16-2 1-Isobutyl-4-piperidone at low price

  • Molecular Formula: C9H17NO
  • Molecular Weight: 155.24
  • Appearance/Colour: colorless to yellow liquid 
  • Melting Point: 28°C (estimate) 
  • Refractive Index: n20/D 1.456(lit.)  
  • Boiling Point: 233.3 °C at 760 mmHg 
  • PKA: 7.94±0.20(Predicted) 
  • Flash Point: 88.3 °C 
  • PSA: 20.31000 
  • Density: 0.94 g/cm3 
  • LogP: 1.24520 

1-Isobutyl-4-piperidone(Cas 72544-16-2) Usage

General Description

1-(2-Methylpropyl)-4-piperidone is a piperidone derivative. It can be synthesized by employing enamine derived from isobutyraldehyde and piperidone as a starting reagent.

InChI:InChI=1/C9H17NO/c1-8(2)7-10-5-3-9(11)4-6-10/h8H,3-7H2,1-2H3

72544-16-2 Relevant articles

Design and synthesis of rho kinase inhibitors (III)

Iwakubo, Masayuki,Takami, Atsuya,Okada, Yuji,Kawata, Takehisa,Tagami, Yoshimichi,Sato, Motoko,Sugiyama, Terumi,Fukushima, Kayoko,Taya, Shinichiro,Amano, Mutsuki,Kaibuchi, Kozo,Iijima, Hiroshi

, p. 1022 - 1033 (2007/10/03)

The structure-activity relationship of R...

Synthesis of heteroarylpiperazines and heteroarylbipiperidines with a restricted side chain and their affinities for 5-HT1A receptor

Yoo, Kyung Ho,Choi, Hyun Sik,Kim, Dong Chan,Shin, Kye Jung,Kim, Dong Jin,Song, Yun Seon,Jin, Changbae

, p. 208 - 215 (2007/10/03)

Heteroarylpiperazine and heteroarylbipip...

Novel 1,4 substituted piperidine derivatives. Synthesis and correlation of antioxidant activity with structure and lipophilicity

Alexidis,Rekka,Demopoulos,Kourounakis

, p. 131 - 137 (2007/10/02)

A series of novel piperidine derivatives...

72544-16-2 Process route

4-piperidone hydrochloride
41979-39-9

4-piperidone hydrochloride

N-(2-methylpropyl)-4-piperidone
72544-16-2

N-(2-methylpropyl)-4-piperidone

Conditions
Conditions Yield
With potassium carbonate; In acetonitrile;
47.8%
1-phenylmethyl-4-piperidone
3612-20-2

1-phenylmethyl-4-piperidone

N-(2-methylpropyl)-4-piperidone
72544-16-2

N-(2-methylpropyl)-4-piperidone

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: 97 percent / H2 ; aq. HCl / palladium hydroxide / ethanol / 24 h / 20 °C / 3102.89 Torr
2: 47.8 percent / K2 CO3 / acetonitrile
With hydrogenchloride; hydrogen; potassium carbonate; palladium dihydroxide; In ethanol; acetonitrile;

72544-16-2 Upstream products

  • 162258-31-3
    162258-31-3

    dimethyl β,β'-isobutylaminodipropionate

  • 88488-91-9
    88488-91-9

    3,3'-isobutylimino-di-propionic acid diethyl ester

  • 25012-73-1
    25012-73-1

    1-isobutyl-4-oxo-piperidine-3-carboxylic acid methyl ester

  • 41979-39-9
    41979-39-9

    4-piperidone hydrochloride

Shopping Cart

Clear Inquiry