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Secobarbital

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Identification
Molecular formula
C12H18N2O3
CAS number
76-73-3
IUPAC name
5-ethyl-5-(1-methylbut-1-enyl)hexahydropyrimidine-2,4,6-trione
State
State

Secobarbital is typically in a solid state at room temperature.

Melting point (Celsius)
137.00
Melting point (Kelvin)
410.15
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.15
General information
Molecular weight
238.29g/mol
Molar mass
238.2880g/mol
Density
1.1610g/cm3
Appearence

Secobarbital appears as a white, odorless, crystalline powder. It is soluble in water and reacts with strong acids and bases, which can alter its structure.

Comment on solubility

Solubility of 5-ethyl-5-(1-methylbut-1-enyl)hexahydropyrimidine-2,4,6-trione

When discussing the solubility of 5-ethyl-5-(1-methylbut-1-enyl)hexahydropyrimidine-2,4,6-trione, several factors come into play:

  • Polarity: The presence of multiple functional groups in the structure indicates that polarity could affect solubility in various solvents.
  • Hydrogen bonding: The ability of this compound to form hydrogen bonds with solvents can enhance solubility in polar solvents.
  • Chemical structure: The bulky ethyl and methyl groups might influence how well the compound integrates into different solvent environments.

Generally, compounds containing similar structures tend to vary in solubility:

  • In polar solvents like water, solubility may be moderate due to potential hydrogen bonding.
  • In non-polar solvents, solubility may be more favorable, linked to the hydrophobic characteristics of the hydrocarbon tail.

In summary, while definitive data on the solubility of 5-ethyl-5-(1-methylbut-1-enyl)hexahydropyrimidine-2,4,6-trione may not be extensively documented, one could anticipate variability based on the solvent environment, leading to unique behaviors in different chemical contexts.

Interesting facts

Interesting Facts about 5-ethyl-5-(1-methylbut-1-enyl)hexahydropyrimidine-2,4,6-trione

5-ethyl-5-(1-methylbut-1-enyl)hexahydropyrimidine-2,4,6-trione is a fascinating compound that showcases the intricate beauty of organic chemistry. This compound belongs to the family of pyrimidines, which are heterocyclic compounds containing a six-membered ring with two nitrogen atoms. Here are some intriguing aspects of this compound:

  • Structural Complexity: The presence of both ethyl and 1-methylbut-1-enyl groups in its structure contributes to its unique physical properties and reactivity, making it an intriguing subject of study.
  • Biological Relevance: The pyrimidine core is pivotal in biological systems, serving as a building block for nucleotides, which comprise DNA and RNA. This compound might have implications in the study of genetic material.
  • Chemical Reactivity: As a dicarbonyl compound, it is likely to participate in various reactions such as condensation and nucleophilic additions, which can lead to the synthesis of other complex organic molecules.
  • Potential Applications: With ongoing research into pyrimidine derivatives, there is potential for discovering novel pharmaceuticals or agrochemicals based on its structure. This compound could serve as a lead structure for developing antitumor or antiviral agents.
  • Historical Context: Pyrimidines were first identified in the late 19th century and have since played a crucial role in expanding our understanding of molecular biology and medicinal chemistry.

As we delve deeper into the study of compounds like 5-ethyl-5-(1-methylbut-1-enyl)hexahydropyrimidine-2,4,6-trione, it becomes evident that the vast world of organic compounds is filled with potential waiting to be unlocked. Each discovery not only enriches our knowledge but also paves the way for innovative solutions to real-world challenges.

Synonyms
SCHEMBL713592
5-ethyl-5-(1-methylbutenyl)barbituric acid