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Phenylbarbituric acid

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Identification
Molecular formula
C9H7N3O2
CAS number
495-71-6
IUPAC name
6-phenyl-1H-1,3,5-triazine-2,4-dione
State
State

At room temperature, phenylbarbituric acid is a solid.

Melting point (Celsius)
222.00
Melting point (Kelvin)
495.15
Boiling point (Celsius)
420.00
Boiling point (Kelvin)
693.15
General information
Molecular weight
203.18g/mol
Molar mass
203.1820g/mol
Density
1.2808g/cm3
Appearence

Phenylbarbituric acid appears as a white crystalline powder.

Comment on solubility

Solubility of 6-phenyl-1H-1,3,5-triazine-2,4-dione

The solubility of 6-phenyl-1H-1,3,5-triazine-2,4-dione in various solvents is a crucial characteristic that influences its applications in chemical synthesis and product formulation. This compound exhibits unique solubility behavior that can be summarized as follows:

  • Polar Solvents: 6-phenyl-1H-1,3,5-triazine-2,4-dione tends to show moderate solubility in polar solvents due to its functional groups that can interact through hydrogen bonding.
  • Non-Polar Solvents: In non-polar solvents, this compound generally exhibits lower solubility owing to its polar character, which leads to limited interactions.
  • Water Solubility: The water solubility of this compound is expected to be low. The presence of hydrophobic phenyl groups hinders its ability to dissolve in aqueous solutions.

As a result, it is essential to consider the choice of solvent when working with 6-phenyl-1H-1,3,5-triazine-2,4-dione in laboratory settings. Optimizing solubility can enhance reaction rates and yield in chemical processes. To quote a common sentiment in chemistry: "Like dissolves like." This highlights the importance of matching the polarity of the solvent to the chemical properties of the solute to achieve effective solubility.

Interesting facts

Interesting Facts about 6-phenyl-1H-1,3,5-triazine-2,4-dione

6-phenyl-1H-1,3,5-triazine-2,4-dione, commonly known as phenyltriazine, is a fascinating compound that showcases the intricacies of chemical bonding and reactivity. Here are some intriguing insights into this compound:

  • Versatile Applications: This compound is often investigated for its potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science. Its unique structure allows it to interact with other molecules in interesting ways.
  • Structural Elegance: The triazine ring offers intriguing geometrical properties and functionalities due to its nitrogen atoms, making it a subject of study in heterocyclic chemistry.
  • Stability and Reactivity: The presence of multiple carbonyl groups contributes to the compound’s stability under standard conditions, while also making it susceptible to nucleophilic attack, leading to diverse chemical reactivity.
  • Research Potential: Scientists are drawn to exploring its synthesis pathways and reactivity for discovering new derivatives, which may possess improved or altered properties suitable for specific applications.
  • Photophysical Properties: This compound has been studied for its light-absorbing capabilities, making it a candidate for further research in the fields of photovoltaics and photoresponsive materials.

In conclusion, the study of 6-phenyl-1H-1,3,5-triazine-2,4-dione is not only important for its chemical properties but also for its potential applications that could impact various industries. With ongoing research, we may unlock even more insights into this fascinating compound!

Synonyms
7459-63-4
6-Phenyl-1,3,5-triazine-2,4(1H,3H)-dione
6-phenyl-1H-1,3,5-triazine-2,4-dione
Triazine-2,4-dihydroxy, 6-phenyl-
EINECS 231-236-4
6-phenyl-5-azauracil
2,4-Dihydroxy-6-phenyl-1,3,5-triazine
SCHEMBL1534218
SCHEMBL10412916
DTXSID30225562
KGKPZSCTAFFXBV-UHFFFAOYSA-N
2-phenyl-4,6-dihydroxy-s-triazine
AKOS006343510
AKOS015964010
6-phenyl-1,3,5-triazine-2,4-dione
AC-22502
NS00037634
6-phenyl-1,3,5-triazin-2,4[1H,3H]-dione