Skip to main content

Amobarbital

ADVERTISEMENT
Identification
Molecular formula
C11H18BrN2O3
CAS number
57-43-2
IUPAC name
5-(2-bromoallyl)-5-(1-methylbutyl)hexahydropyrimidine-2,4,6-trione
State
State
Solid
Melting point (Celsius)
156.00
Melting point (Kelvin)
429.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
226.24g/mol
Molar mass
226.2390g/mol
Density
1.1900g/cm3
Appearence
Amobarbital is typically a white, odorless crystalline powder. It can be pressed into tablet form or used in a solution for medical applications.
Comment on solubility

Solubility of 5-(2-bromoallyl)-5-(1-methylbutyl)hexahydropyrimidine-2,4,6-trione

The solubility of 5-(2-bromoallyl)-5-(1-methylbutyl)hexahydropyrimidine-2,4,6-trione in various solvents can significantly influence its applications in chemical processes. Understanding the solubility behavior of this compound is crucial for its effective utilization.

Key Points on Solubility:

  • Polarity: The presence of multiple functional groups suggests a degree of polarity that could affect solubility in polar solvents such as water.
  • Hydrophilicity vs. Hydrophobicity: The bromo allyl and methylbutyl groups may impart hydrophobic characteristics, potentially limiting solubility in aqueous environments.
  • Organic Solvents: It is likely to show greater solubility in organic solvents like ethanol, methanol, or dimethyl sulfoxide (DMSO), which can better accommodate non-polar regions.
  • Temperature Influence: Increasing temperature can often enhance solubility, making solvent choice and temperature control vital during experiments.

As stated, “Like dissolves like.” Thus, the solubility of this compound is highly dependent on the solvent's polarity. Experimentation and characterization through various solubility tests will provide valuable insights into its behavior in different environments.

Interesting facts

Interesting Facts about 5-(2-bromoallyl)-5-(1-methylbutyl)hexahydropyrimidine-2,4,6-trione

The compound 5-(2-bromoallyl)-5-(1-methylbutyl)hexahydropyrimidine-2,4,6-trione is a fascinating example of a synthetic organic molecule that showcases the complexity and creativity of modern chemistry. Here are some intriguing facts:

  • Chemical Structure: This compound belongs to the class of hexahydropyrimidines, which are notable for their six-membered rings containing nitrogen atoms. The diverse substitutions on the pyrimidine ring contribute to its unique reactivity and potential applications.
  • Bridging Compounds: The incorporation of the bromoallyl group enhances the molecule's ability to participate in various chemical reactions, such as nucleophilic substitutions, making it a valuable intermediate in organic synthesis.
  • Potential Applications: Compounds like this one can serve as precursors for pharmaceuticals. Their structural features may lend themselves to bioactivity, potentially influencing *enzyme inhibition* or *antimicrobial activity*.
  • Research Implications: Understanding the reactivity and synthesis of compounds such as this can contribute to the development of new methodologies in synthetic organic chemistry, paving the way for innovative *drug design* and *material science*.
  • Chemical Stability: The stable nature of the hexahydropyrimidine ring makes it a subject of research for dynamic equilibrium and reaction pathways, providing insights into thermodynamics and kinetics in chemical reactions.

The study of compounds like 5-(2-bromoallyl)-5-(1-methylbutyl)hexahydropyrimidine-2,4,6-trione not only deepens our understanding of complex organic chemistry but also opens doors to future discoveries and applications in various scientific fields.

Synonyms
Sigmodal
1216-40-6
5-(2-Bromoallyl)-5-(1-methylbutyl)-1H,3H,5H-pyrimidine-2,4,6-trione
5-(2-bromoprop-2-enyl)-5-pentan-2-yl-1,3-diazinane-2,4,6-trione
8N609W64JZ
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-(2-bromo-2-propenyl)-5-(1-methylbutyl)-
5-(.beta.-Bromoallyl)-5-(1-methylbutyl)barbituric acid
Recton
UNII-8N609W64JZ
EINECS 214-932-2
Barbituric acid, 5-(2-bromoallyl)-5-(1-methylbutyl)-
DTXSID90874338
5-(2-BROMOALLYL)-5-(1-METHYLBUTYL) BARBITURIC ACID
NS00010480
Q7512448
5-(2-Bromoallyl)-5-sec-pentyl-1H,3>H,5H-pyrimidine-2,4,6-trione
2,4,6(1H,3H,5H)-PYRIMIDINETRIONE, 5-(2-BROMO-2-PROPEN-1-YL)-5-(1-METHYLBUTYL)-
5-(2-Bromo-2-propenyl)-5-(1-methylbutyl)-2,4,6(1H,3H,5H)-pyrimidinetrione #