Ethyl N-piperazinecarboxylate
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
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)
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
- Language:English Provider:Ethyl N-piperazinecarboxylate
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
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
Ethyl N-piperazinecarboxylate Preparation Products And Raw materials
Raw materials
Preparation Products
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