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Ethyl (3-aminosulfanyl-methylidene)hydrazono)-butanoate

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Identification
Molecular formula
C7H13N3O2S
CAS number
.7607
IUPAC name
ethyl 3-[[amino(sulfanyl)methylene]hydrazono]butanoate
State
State

At room temperature, ethyl (3-aminosulfanyl-methylidene)hydrazono)-butanoate exists as a solid and it is typically stable under standard laboratory conditions.

Melting point (Celsius)
112.00
Melting point (Kelvin)
285.15
Boiling point (Celsius)
327.50
Boiling point (Kelvin)
600.65
General information
Molecular weight
189.26g/mol
Molar mass
189.2500g/mol
Density
1.1863g/cm3
Appearence

The compound ethyl (3-aminosulfanyl-methylidene)hydrazono)-butanoate appears as a yellow-orange crystalline solid. Its physical appearance may vary slightly with purity and packaging.

Comment on solubility

Solubility of Ethyl 3-[[amino(sulfanyl)methylene]hydrazono]butanoate

The solubility of ethyl 3-[[amino(sulfanyl)methylene]hydrazono]butanoate can provide significant insights into its potential applications and behavior in various environments. Understanding its solubility is essential because:

  • It dictates how the compound can interact with other substances.
  • It influences the compound's bioavailability—essential for pharmaceuticals.
  • It affects the transport and distribution in chemical processes.

In general, the solubility of this compound can be influenced by several factors:

  • Polarity: Compounds with polar functional groups typically exhibit higher solubility in polar solvents, such as water.
  • Temperature: Increased temperature often enhances solubility, allowing more of the compound to dissolve.
  • pH Levels: The solubility may vary with changes in pH due to protonation or deprotonation of functional groups.
  • Presence of Other Solutes: The solubility can be affected by the presence of salts or other solutes due to common ion effects.

Researchers have noted that certain structural features of the compound may help predict its solubility behavior. For example, the presence of amino or hydrazono groups can enhance hydrogen bonding with water molecules, potentially increasing solubility.

In sum, while detailing the solubility of ethyl 3-[[amino(sulfanyl)methylene]hydrazono]butanoate, one should consider its structural characteristics and the specific conditions under which it is being analyzed. These parameters together can provide crucial data for practical applications.

Interesting facts

Interesting Facts about Ethyl 3-[[amino(sulfanyl)methylene]hydrazono]butanoate

Ethyl 3-[[amino(sulfanyl)methylene]hydrazono]butanoate is a fascinating compound that showcases the ingenuity of chemical synthesis and the diverse applications of organic chemistry. Here are some intriguing aspects of this compound:

  • Composition and Structure: This compound features a unique combination of functional groups, including an amino group, a sulfanyl group, and a hydrazone linkage. This diversity allows for a variety of chemical reactivity and interactions.
  • Biological Interest: Due to its structural properties, compounds like this one may exhibit biological activities. Studies in medicinal chemistry often explore such compounds for potential anti-inflammatory and antimicrobial properties.
  • Synthetic Routes: The synthesis of ethyl 3-[[amino(sulfanyl)methylene]hydrazono]butanoate involves clever synthetic strategies that utilize hydrazones and thiol derivatives, highlighting the creativity required in organic synthesis.
  • Applications in Research: Scientists utilize this compound in various fields of research, particularly in the development of new pharmaceuticals or agrochemicals, as the reactivity of its functional groups can lead to novel compounds with valuable properties.
  • Interdisciplinary Connections: The study of such compounds bridges several fields, including organic chemistry, biochemistry, and pharmacology, showcasing the interdisciplinary nature of modern scientific research.

In summary, ethyl 3-[[amino(sulfanyl)methylene]hydrazono]butanoate is not just a chemical compound; it is a testament to the complexity and beauty of chemical interactions, with potential implications in both academic research and practical applications. As one researcher noted, "The exploration of new compounds often leads to unexpected discoveries that drive innovation."