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Phenthion

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Identification
Molecular formula
C15H18N2O2
CAS number
299-84-3
IUPAC name
1-cyclohexyl-2-phenyl-1,2,4-triazolidine-3,5-dione
State
State

Phenthion is typically found in a solid state at room temperature.

Melting point (Celsius)
92.00
Melting point (Kelvin)
365.15
Boiling point (Celsius)
372.50
Boiling point (Kelvin)
645.70
General information
Molecular weight
246.29g/mol
Molar mass
246.2920g/mol
Density
1.2132g/cm3
Appearence

Phenthion is an off-white crystalline solid.

Comment on solubility

Solubility of 1-cyclohexyl-2-phenyl-1,2,4-triazolidine-3,5-dione

The solubility of 1-cyclohexyl-2-phenyl-1,2,4-triazolidine-3,5-dione in various solvents can significantly influence its applications and behavior in chemical reactions. This compound exhibits unique properties due to its structural characteristics, and understanding its solubility is essential for practical uses.

Factors Influencing Solubility:

  • Polar vs. Non-Polar Solvents: Given the presence of both cyclohexyl and phenyl groups, this compound tends to be more soluble in non-polar solvents.
  • Temperature: Higher temperatures often increase solubility, particularly for organic compounds.
  • pH of Solution: The ionization of functional groups can alter solubility; however, since this compound lacks strongly acidic or basic groups, pH effects are likely minimal.

As with many organic compounds, the solubility may be described in terms of "like dissolves like," where similar polarities lead to better solubility. In conclusion, while 1-cyclohexyl-2-phenyl-1,2,4-triazolidine-3,5-dione generally shows better solubility in non-polar solvents, further analytical studies would be beneficial to provide precise solubility data in various environments.

Interesting facts

Interesting Facts about 1-Cyclohexyl-2-phenyl-1,2,4-triazolidine-3,5-dione

The compound 1-cyclohexyl-2-phenyl-1,2,4-triazolidine-3,5-dione is a fascinating member of the triazolidine family of compounds. Here are some intriguing aspects:

  • Structural Diversity: This compound exhibits a unique structure that combines cyclic and aromatic components, making it an interesting case for study in organic chemistry.
  • Biological Activity: Compounds in the triazolidine family have shown promise in various biological applications. Research indicates that derivatives of this compound might exhibit antioxidant properties, thus highlighting their potential in medicinal chemistry.
  • Synthetic Pathways: The synthesis of 1-cyclohexyl-2-phenyl-1,2,4-triazolidine-3,5-dione involves innovative organic reactions that can be a great teaching tool for students learning about multi-step synthesis processes.
  • Pharmaceutical Relevance: Structurally related compounds have been investigated for their roles in drug development; thus, understanding compounds like this one could lead to new therapeutic agents.
  • Interdisciplinary Connections: The study of this compound intersects various fields, including medicinal chemistry, material science, and even biochemistry, due to its potential applications.

Overall, 1-cyclohexyl-2-phenyl-1,2,4-triazolidine-3,5-dione serves not only as a subject of academic interest but also as a platform for exploring new research avenues in diverse scientific fields.

Synonyms
BICARBAMIMIDE, N-CYCLOHEXYL-2-PHENYL-
3657-61-2
NIOSH/DT4393350
2-Cyclohexyl-3-phenylbicarbamimide
UR 65
Bicarbamimide, 2-cyclohexyl-3-phenyl-
DT43933500
1,2,4-Triazolidine-3,5-dione, 1-cyclohexyl-2-phenyl-
UR 111
N-Cyclohexyl-2-phenylbicarbamimide
BRN 0891256
1,2,4-Triazolidine-3,5-dione, 4-cyclohexyl-2-phenyl-
5-26-05-00240 (Beilstein Handbook Reference)
DTXSID70190068