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2-Ethylsulfanylethyl pyridine-3-carboxylate

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Identification
Molecular formula
C10H13NO2S
CAS number
1234567-89-0
IUPAC name
2-ethylsulfanylethyl pyridine-3-carboxylate
State
State

At room temperature, 2-ethylsulfanylethyl pyridine-3-carboxylate exists as a liquid. It's important for handling and working with this compound to avoid inhalation of vapors and skin contact due to its potential irritant properties.

Melting point (Celsius)
14.00
Melting point (Kelvin)
287.15
Boiling point (Celsius)
287.00
Boiling point (Kelvin)
560.15
General information
Molecular weight
207.29g/mol
Molar mass
207.2860g/mol
Density
1.2083g/cm3
Appearence

2-Ethylsulfanylethyl pyridine-3-carboxylate, often utilized in chemical laboratories, typically appears as a colorless to pale yellow liquid. This compound holds a clean appearance and lacks significant particulate matter, which is an indication of its purity when synthesized or stored correctly. It may darken slightly over time upon prolonged exposure to air and light, which might indicate the onset of decomposition or impurity formation.

Comment on solubility

Solubility of 2-ethylsulfanylethyl pyridine-3-carboxylate

The solubility of 2-ethylsulfanylethyl pyridine-3-carboxylate is influenced by several factors, making it a compound of interest in both chemical synthesis and applications. Understanding its solubility characteristics involves evaluating various aspects, such as:

  • Polarity: Due to the presence of the pyridine ring and ethylsulfanyl group, this compound exhibits a degree of polarity. Polar solvents such as water may facilitate dissolution, although the overall solubility may vary.
  • Solvent Interaction: The solubility can be significantly affected depending on the solvent used. In polar protic solvents, the interactions with the functional groups can enhance solubility.
  • Temperature: As is typical with many compounds, solubility may increase with temperature. This thermodynamic principle is crucial when considering dissolution rates and behaviors in practical applications.
  • pH Levels: The ionization of the carboxylate group can also affect solubility, as increasing pH can promote ion formation, potentially increasing solubility in aqueous environments.

Overall, while 2-ethylsulfanylethyl pyridine-3-carboxylate may not exhibit extensive solubility across all media, its behavior in various solvents and conditions can provide insights into its applicability in different chemical reactions and processes.

Interesting facts

Interesting Facts about 2-Ethylsulfanylethyl Pyridine-3-Carboxylate

2-Ethylsulfanylethyl pyridine-3-carboxylate is a fascinating compound with intriguing properties and applications. Here are some noteworthy points:

  • Structural Features: This compound features a pyridine ring, known for its role in many biological systems, which contributes to its potential in medicinal chemistry.
  • Diverse Applications: Compounds like 2-ethylsulfanylethyl pyridine-3-carboxylate have shown promise in organic synthesis, as well as in the development of pharmaceuticals, particularly due to their ability to act as intermediates.
  • Biological Activity: The pyridine moiety often exhibits interesting biological activities, including anti-inflammatory and antimicrobial properties, making such compounds of interest in drug development.
  • Functionality: The presence of the ethylsulfanyl group can enhance the solubility and accessibility of the compound in various chemical reactions, paving the way for innovative synthesis methods.
  • Research Significance: Its unique structural attributes make 2-ethylsulfanylethyl pyridine-3-carboxylate a point of interest in ongoing research, particularly in creating new molecules with enhanced activity or selectivity.

As with many compounds in the field of organic chemistry, understanding 2-ethylsulfanylethyl pyridine-3-carboxylate opens doors to the development of new technologies and innovations, underlining the significance of such compounds in both academic and practical contexts.

Synonyms
2-(Ethylthio)ethyl nicotinate
27868-70-8
BRN 0389736
NICOTINIC ACID, 2-(ETHYLTHIO)ETHYL ESTER
DTXSID40182172
5-22-05-00108 (Beilstein Handbook Reference)
RefChem:365634
DTXCID50104663
3-Pyridinecarboxylicacid, 2-(ethylthio)-, ethyl ester