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4-amino-3-methylthio-6-phenyl-4H-pyridazin-5-one

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Identification
Molecular formula
C11H11N3OS
CAS number
>104735-89-5
IUPAC name
4-amino-3-methylsulfanyl-6-phenyl-4H-pyridazin-5-one
State
State

At room temperature, this compound is in a solid state.

Melting point (Celsius)
218.00
Melting point (Kelvin)
491.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
247.30g/mol
Molar mass
247.3030g/mol
Density
1.3225g/cm3
Appearence

This compound typically appears as a crystalline solid with a pale yellow to off-white coloration. The crystals can sometimes be seen as needles or prisms.

Comment on solubility

Solubility of 4-amino-3-methylsulfanyl-6-phenyl-4H-pyridazin-5-one

The solubility of 4-amino-3-methylsulfanyl-6-phenyl-4H-pyridazin-5-one is an important characteristic to consider when evaluating its potential applications. This compound exhibits moderate solubility in various solvents, and its solubility can be influenced by several factors:

  • Polarity: The presence of amino and methylsulfanyl groups suggests that the compound may be more soluble in polar solvents, such as water and alcohols, compared to nonpolar solvents.
  • Temperature: Solubility is generally temperature-dependent. Increased temperature often enhances the solubility of organic compounds.
  • pH Levels: The ionization state of the amino group may vary with pH, affecting solubility in aqueous solutions. In more acidic or basic environments, the solubility can change dramatically.

It is essential to conduct empirical solubility tests to determine specific values, as "solubility is a multifaceted property that can vary with conditions." Overall, this compound demonstrates a balance between hydrophilic and hydrophobic characteristics, making it versatile for various chemical applications.

Interesting facts

Interesting Facts about 4-amino-3-methylsulfanyl-6-phenyl-4H-pyridazin-5-one

The compound 4-amino-3-methylsulfanyl-6-phenyl-4H-pyridazin-5-one is an intriguing member of the pyridazine family, which is known for its unique chemical properties and potential applications. Here are some captivating aspects of this compound:

  • Structural Characteristics: This compound features a pyridazine ring, which is a six-membered aromatic heterocycle containing two nitrogen atoms. Its complex structure showcases various functional groups that contribute to its biological activity.
  • Biological Significance: Compounds similar to 4-amino-3-methylsulfanyl-6-phenyl-4H-pyridazin-5-one have been studied for their pharmacological properties, including anti-inflammatory and analgesic effects. The presence of amino and sulfanyl groups enhances its reactivity and can affect its biological interactions.
  • Potential Applications: This compound holds promise in medicinal chemistry, particularly in drug development targeting various diseases. Researchers are exploring its potential use in the synthesis of novel therapeutic agents.
  • Chemical Reactivity: The amino group (-NH2) in its structure allows for nucleophilic attacks in chemical reactions, which can lead to the formation of derivatives. This reactivity paves the way for further modifications and functionalization in synthetic chemistry.
  • Cytotoxicity Studies: Initial studies have indicated that similar compounds exhibit cytotoxic effects on certain cancer cell lines, prompting further investigations into their mechanisms of action and potential as anticancer agents.

In summary, 4-amino-3-methylsulfanyl-6-phenyl-4H-pyridazin-5-one is not just a compound of chemical interest; it embodies a rich landscape for exploration in both academic research and potential therapeutic applications. As scientists delve deeper, its multifaceted properties could lead to groundbreaking discoveries in medicinal chemistry.