29976-53-2

  • Product Name:N-Carbethoxy-4-piperidone
  • Molecular Formula:C8H13NO3
  • Purity:99%
  • Molecular Weight:171.196
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Product Details;

CasNo: 29976-53-2

Molecular Formula: C8H13NO3

Appearance: Clear colorless to pale yellow colored liquid

Chinese Manufacturer Supply N-Carbethoxy-4-piperidone, Export 29976-53-2 with Low Price

  • Molecular Formula:C8H13NO3
  • Molecular Weight:171.196
  • Appearance/Colour:Clear colorless to pale yellow colored liquid 
  • Vapor Pressure:0.00574mmHg at 25°C 
  • Refractive Index:n20/D 1.475(lit.)  
  • Boiling Point:273.4 °C at 760 mmHg 
  • PKA:-1.59±0.20(Predicted) 
  • Flash Point:87.8 °C 
  • PSA:46.61000 
  • Density:1.155 g/cm3 
  • LogP:0.74570 

N-Carbethoxy-4-piperidone(Cas 29976-53-2) Usage

Chemical Properties

clear colorless to pale yellow colored liquid

Uses

N-Carbethoxy-4-piperidone is used in the preparation of 3-hydrazinopyridazines as antihypertensive agents as well as γ-carboline derivatives as potential serotonergic agents. N-Carbethoxy-4-piperidone is also an Impurity of Loratadine (L469575).

InChI:InChI=1/C8H13NO3/c1-2-12-8(11)9-5-3-7(10)4-6-9/h2-6H2,1H3

29976-53-2 Relevant articles

Ecotoxic effects of loratadine and its metabolic and light-induced derivatives

Iesce, Maria Rosaria,Lavorgna, Margherita,Russo, Chiara,Piscitelli, Concetta,Passananti, Monica,Temussi, Fabio,DellaGreca, Marina,Cermola, Flavio,Isidori, Marina

, p. 664 - 672 (2019/01/03)

Loratadine and desloratadine are second-...

Development of a Robust Process for the Preparation of High-Quality 4-Methylenepiperidine Hydrochloride

Zhu, Fuqiang,Aisa, Haji A.,Zhang, Jian,Hu, Tianwen,Sun, Changliang,He, Yang,Xie, Yuanchao,Shen, Jingshan

, p. 91 - 96 (2018/02/06)

An efficient route for the preparation o...

New synthesis of (±)-2-piperazinecarboxylic acid.

JY Mérour, JY Coadou

, Tetrahedron letters, 1991

(±)-2-Piperazinecarboxylic acid is prepared from N-carbethoxy-4-piperidone by α Schmidt rearrangement followed by bromation of the lactam; then α Favorskii rearrangement on the experiment....

29976-53-2 Process route

4-piperidone hydrochloride
41979-39-9

4-piperidone hydrochloride

chloroformic acid ethyl ester
541-41-3

chloroformic acid ethyl ester

N-ethoxycarbonyl-4-piperidone
29976-53-2

N-ethoxycarbonyl-4-piperidone

Conditions
Conditions Yield
With triethylamine; In dichloromethane; at 0 - 20 ℃; for 2h;
98%
With triethylamine; In dichloromethane; at 0 - 20 ℃; for 2h;
98%
With sodium hydroxide; In diethyl ether; water; at 0 ℃; for 0.166667h;
93%
4-oxo-piperidine-1,3-dicarboxylic acid diethyl ester
53601-94-8

4-oxo-piperidine-1,3-dicarboxylic acid diethyl ester

N-ethoxycarbonyl-4-piperidone
29976-53-2

N-ethoxycarbonyl-4-piperidone

Conditions
Conditions Yield
With hydrogenchloride; In ethanol; water; at 83 - 85 ℃; for 7h;
98.2%

29976-53-2 Upstream products

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    1445-73-4

    1-Methyl-4-piperidone

  • 541-41-3
    541-41-3

    chloroformic acid ethyl ester

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    4-piperidone hydrochloride

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    1,4-dioxa-8-aza-spiro[4.5]decane-8-carboxylic acid ethyl ester

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    5-oxoazepane-1,4-dicarboxylic acid diethyl ester

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    4-Benzoyloxy-4-isoquinolin-1-yl-piperidine-1-carboxylic acid ethyl ester

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