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Ethyl piperazine-1-carboxylate

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Identification
Molecular formula
C7H14N2O2
CAS number
120-23-0
IUPAC name
ethyl piperazine-1-carboxylate
State
State

At room temperature, ethyl piperazine-1-carboxylate is typically in a liquid state.

Melting point (Celsius)
-5.00
Melting point (Kelvin)
268.15
Boiling point (Celsius)
223.00
Boiling point (Kelvin)
496.15
General information
Molecular weight
158.20g/mol
Molar mass
158.1990g/mol
Density
1.1200g/cm3
Appearence

Ethyl piperazine-1-carboxylate is typically a colorless liquid that might sometimes appear to have a slight yellow tint. It is often encountered in a clear form with no visible impurities and is primarily used in laboratory settings.

Comment on solubility

Solubility of Ethyl Piperazine-1-carboxylate

Ethyl piperazine-1-carboxylate is known for its interesting solubility characteristics, which can be attributed to its functional groups and molecular structure. Here are some points to consider:

  • Polar Nature: Due to the presence of the carboxylate group, this compound exhibits a significant degree of polarity.
  • Solvents: Ethyl piperazine-1-carboxylate is generally soluble in:
    • Water
    • Alcohols
    • Some organic solvents
  • Temperature Influence: Solubility tends to increase with temperature, making it more soluble in hot solvents.
  • pH Sensitivity: The solubility can be affected by the pH of the solution due to the ionization of the carboxylate group.

In summary, the solubility of ethyl piperazine-1-carboxylate is favorable in polar solvents, which makes it suitable for a variety of applications in pharmaceutical and chemical industries.

Interesting facts

Interesting Facts about Ethyl Piperazine-1-Carboxylate

Ethyl piperazine-1-carboxylate is a fascinating compound that has sparked the interest of many scientists due to its unique structure and versatility. Here are some notable aspects of this compound:

  • Pharmaceutical Relevance: Ethyl piperazine-1-carboxylate is often studied for its potential as a precursor in the synthesis of various pharmacologically active agents. Its structure makes it a good candidate for modifications that can lead to new drug discoveries.
  • Diverse Applications: Beyond pharmaceuticals, this compound has found applications in fields such as agriculture and materials science. Its properties may lend themselves to innovations in agrochemicals or polymer chemistry.
  • Research Interest: According to various studies, piperazine derivatives are known for their multifunctional capabilities, which pique the interest of chemists looking to develop new therapeutic compounds.
  • Chemical Versatility: The presence of both ethyl and piperazine groups in its structure allows for a wide range of chemical reactions and transformations, making it a valuable compound in synthetic organic chemistry.
  • Emphasis on Safety: As with many chemical compounds, understanding the safety profiles of ethyl piperazine-1-carboxylate is essential. Proper handling and disposal are crucial, as they contribute to effective laboratory practices.

In summary, ethyl piperazine-1-carboxylate stands out as a compound worthy of attention in both academic and industrial settings due to its versatile applications and potential for innovative research. Its role in synthesizing new compounds could make a significant impact in the future of drug development and other chemical productions.

Synonyms
120-43-4
Ethyl piperazine-1-carboxylate
Ethyl N-piperazinecarboxylate
Ethyl 1-piperazinecarboxylate
N-Carbethoxypiperazine
1-PIPERAZINECARBOXYLIC ACID, ETHYL ESTER
1-Carbethoxypiperazine
N-(Ethoxycarbonyl)piperazine
1-Carboethoxypiperazine
1-(Ethoxycarbonyl)piperazine
Ethyl 1-piperazinocarboxylate
Piperazine ethylcarboxylate
Ethylcarbonyl piperazine
1-Ethoxycarbonylpiperazine
Piperazine-1-carboxylic acid ethyl ester
N-ethoxycarbonylpiperazine
EINECS 204-395-2
Ethyl N-piperazinocarboxylate
MFCD00005964
NSC 21060
BRN 0125780
n-carboethoxypiperazine
ethoxycarbonylpiperazine
Piperazine-N-carboxylic acid ethyl ester
DTXSID7059511
5-23-01-00055 (Beilstein Handbook Reference)
NSC-21060
1-Piperazinecarboxylic Acid Ethyl Ester
Ethyl N-piperazinecartoxylate
n-carbethoxy piperazine
ethyl piperazinecarboxylate
carbethoxypiperazine
1-carbethoxy-piperazine
1-Carbethoxy piperazine
ethoxycarbonyl piperazine
ethyloxycarbonylpiperazine
ethyl piperazincarboxylate
4-ethoxycarbonylpiperazine
1-ethoxycarbonyl piperazine
1-ethoxycarbonyl-piperazine
4-ethoxycarbonyl-piperazine
ethyl piperazine carboxylate
ethyl 1-piperazincarboxylate
ethyl-n-piperazinocarboxylate
N-ethoxy carbonyl piperazine
4-ethoxy carbonyl piperazine
ethyl I-piperazinecarboxylate
Ethyl-1-piperizinecarboxylate
Ethylpiperazine-1-carboxylate
ethyl 1-piperazinylcarboxylate
ethyl-N-piperazine carboxylate
piperazine, 1-ethoxycarbonyl-
SCHEMBL113765
ethyl 1-piperazine carboxylate
ethyl 1-piperazine-carboxylate
ethyl 1-piperazinec-arboxylate
ethyl piperazine-4-carboxylate
ethyl-1-piperazine carboxylate
ethyl-1-piperizine carboxylate
CHEMBL213851
DTXCID1033535
29325GHS9J
ALBB-032912
NSC21060
NSC22134
Ethyl 1-piperazinecarboxylate, 99%
NSC-22134
STL384206
piperazinecarboxylic acid, ethyl ester
AKOS000119682
CS-W013283
FE43681
SB40708
N-piperazine carboxylic acid ethyl ester
DS-13407
DB-002720
NS00023917
P1349
EN300-20101
AE-018/31864003
Q24008333
F2190-0345
Z104476848