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Ethyl N-piperazinecarboxylate

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Ethyl N-piperazinecarboxylate Basic information

Product Name:
Ethyl N-piperazinecarboxylate
Synonyms:
  • Ethoxycarbonyl piperazine
  • Ethyl N-piperazinecartoxylate
  • 1-Ethoxycarbonylpiperazine ,99%
  • Ethyl N-piperazinecarboxylate, 99% 25GR
  • 1-Ethoxycarbonylpiperazine 1-Piperazinecarboxylic Acid Ethyl Ester
  • 1-ETHOXYCARBONYL PIPERAZINE FOR SYNTHESI
  • N-Carboethoxypiperazine 1-Carboethoxy piperazine
  • 1-Ethoxycarbonyl piperazine for synthesis
CAS:
120-43-4
MF:
C7H14N2O2
MW:
158.2
EINECS:
204-395-2
Product Categories:
  • Piperidines, Piperidones, Piperazines
  • PIPERIDINE
  • 1
Mol File:
120-43-4.mol
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Ethyl N-piperazinecarboxylate Chemical Properties

Melting point:
120 °C
Boiling point:
273 °C (lit.)
Density 
1.08 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.477(lit.)
Flash point:
>230 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
Oily Liquid
pka
8.50±0.10(Predicted)
color 
Clear light yellow
Water Solubility 
soluble
BRN 
125780
CAS DataBase Reference
120-43-4(CAS DataBase Reference)
NIST Chemistry Reference
1-Piperazinecarboxylic acid, ethyl ester(120-43-4)
EPA Substance Registry System
1-Piperazinecarboxylic acid, ethyl ester (120-43-4)
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Safety Information

Hazard Codes 
Xn,T
Risk Statements 
22-36/37/38-20/21/22
Safety Statements 
23-24/25-37/39-26-36
RIDADR 
UN 2810 6.1/PG 3
WGK Germany 
3
RTECS 
TL1378000
Hazard Note 
Toxic
TSCA 
Yes
HazardClass 
6.1(b)
PackingGroup 
III
HS Code 
29335995

MSDS

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Ethyl N-piperazinecarboxylate Usage And Synthesis

Chemical Properties

clear light yellow oily liquid

Uses

Intermediate.

Synthesis

110-85-0

541-41-3

120-43-4

Piperazine (2 g, 23.2 mmol) and deionized water (10 mL) were added to a reaction flask and stirred at 25 °C until completely dissolved, then cooled to 0 °C. A methanol solution (20 mL) of ethyl chloroformate (1.26 g, 11.6 mmol) was slowly added dropwise with stirring. After the dropwise addition was completed, the reaction system was warmed to 25 °C and stirring was continued for 4 hours. Upon completion of the reaction, saturated aqueous sodium chloride solution (30 mL) and dichloromethane (200 mL) were added to the reaction solution for extraction and separation. The organic layer was collected and dried with anhydrous sodium sulfate. The organic solvent was removed by distillation under reduced pressure, and the resulting crude product was purified by column chromatography (eluent: dichloromethane/methanol, 40:1, v/v/v/v) to give ethyl N-piperazinecarboxylate (0.62 g, 33.7% yield) as a white solid.

References

[1] Patent: CN103664899, 2017, B. Location in patent: Paragraph 0465-0469
[2] Patent: CN103664925, 2018, B. Location in patent: Paragraph 0458; 0461; 0462
[3] Journal of the Chemical Society, 1929, p. 50
[4] Journal of Organic Chemistry, 1948, vol. 13, p. 134,138
[5] Chemische Berichte, 1933, vol. 66, p. 113,116

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