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Ethyl 4-nitrosopiperazine-1-carboxylate

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Identification
Molecular formula
C8H13N3O3
CAS number
7664-41-7
IUPAC name
ethyl 4-nitrosopiperazine-1-carboxylate
State
State

At room temperature, Ethyl 4-nitrosopiperazine-1-carboxylate is typically found in a solid state. It might exist as a crystalline solid or as a powder depending on the specific conditions used during its preparation.

Melting point (Celsius)
71.00
Melting point (Kelvin)
344.15
Boiling point (Celsius)
274.00
Boiling point (Kelvin)
547.15
General information
Molecular weight
215.21g/mol
Molar mass
215.2250g/mol
Density
1.2725g/cm3
Appearence

Ethyl 4-nitrosopiperazine-1-carboxylate appears as a pale yellow to yellow crystalline solid. It may also appear as a powder. Being a nitroso compound, it can be light-sensitive and should be stored appropriately to prevent degradation.

Comment on solubility

Solubility of Ethyl 4-Nitrosopiperazine-1-carboxylate

The solubility of Ethyl 4-nitrosopiperazine-1-carboxylate (C8H13N3O3) can be influenced by several factors, making it a subject of interest for chemists. Understanding its solubility characteristics is key for various applications. Here are some crucial points regarding its solubility:

  • Solvent Polarity: Ethyl 4-nitrosopiperazine-1-carboxylate is expected to be more soluble in polar solvents due to the presence of functional groups like the nitroso and carboxylate moieties.
  • Temperature Influence: An increase in temperature typically enhances solubility for many organic compounds, and this may apply to this compound as well.
  • pH Dependence: The ionization of the carboxylate group can vary with pH, thus modifying the solubility profile. In acidic conditions, the compound may have altered solubility characteristics.

A notable quotation regarding solubility can be summarized as follows: “Like dissolves like.” This statement emphasizes that polar molecules tend to dissolve in polar solvents, whereas nonpolar molecules prefer nonpolar solvents.

In conclusion, the solubility of Ethyl 4-nitrosopiperazine-1-carboxylate is dictated by a balance of molecular structure, environmental factors, and solvent characteristics, making it crucial to consider these elements when predicting its behavior in different conditions.

Interesting facts

Interesting Facts About Ethyl 4-Nitrosopiperazine-1-Carboxylate

Ethyl 4-nitrosopiperazine-1-carboxylate is a fascinating compound with unique structural properties and various applications in biochemical research. Here are some intriguing points about this compound:

  • Chemical Structure: This compound features a piperazine ring, which is a six-membered nitrogen-containing heterocycle. The presence of a nitroso group (-NO) introduces interesting reactivity, making it a potential candidate for various chemical transformations.
  • Biological Implications: Compounds containing nitroso groups have been studied for their potential effects on biological systems. They may play roles in nitric oxide signaling and can act as prodrugs in certain medicinal contexts.
  • Analytical Applications: Ethyl 4-nitrosopiperazine-1-carboxylate can be used as a reagent in the synthesis of other complex molecules. Its unique functional groups can serve as intermediates in organic synthesis processes.
  • Research Potential: Due to its structural characteristics, this compound might be investigated for antiparasitic or antimicrobial properties, offering further avenues for pharmaceutical development.
  • Safety Considerations: Nitrosamines, which are closely related to compounds like ethyl 4-nitrosopiperazine-1-carboxylate, are known for their potential carcinogenic properties. Researchers must handle such compounds with care to ensure safety in laboratory settings.

In summary, the study of ethyl 4-nitrosopiperazine-1-carboxylate reveals its multifaceted nature as a chemical entity with implications for both academic research and potential real-world applications. Its interesting blend of structural features and reactivity places it among compounds worthy of further exploration in the fields of organic and medicinal chemistry.

Synonyms
13256-15-0
Ethyl 4-nitroso-1-piperazinecarboxylate
N-Nitroso-N'-carbethoxypiperazine
1-PIPERAZINECARBOXYLIC ACID, 4-NITROSO-, ETHYL ESTER
BRN 0166941
N-Nitroso-N'-carbaethoxypiperazin
UNII-D8K56V729T
N-Nitroso-N'-carbaethoxypiperazin [German]
D8K56V729T
DTXSID50157619
DTXCID5080110
1-Piperazinecarboxylic acid, 4-nitroso-ethyl ester
5-23-03-00219 (beilstein handbook reference)
oyhrviljshwjae-uhfffaoysa-n
ethyl 4-nitrosopiperazine-1-carboxylate
4-NITROSOPIPERAZINE-1-CARBOXYLIC*ACID ETHYL ESTER
4-Nitrosopiperazine-1-carboxylic acid ethyl ester
CHEMBL350935
EN300-24209285
1-Piperazinecarboxylic acid, 4-nitroso- ethyl ester
Q27276250
Z1255419369