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BZP (Benzylpiperazine)

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Identification
Molecular formula
C12H16N2O3
CAS number
3403-76-3
IUPAC name
5-benzyl-1,3-dimethyl-hexahydropyrimidine-2,4,6-trione
State
State

At room temperature, it is a solid compound, typically in a crystalline powder form.

Melting point (Celsius)
228.00
Melting point (Kelvin)
501.15
Boiling point (Celsius)
528.20
Boiling point (Kelvin)
801.35
General information
Molecular weight
246.27g/mol
Molar mass
246.3000g/mol
Density
1.3000g/cm3
Appearence

5-Benzyl-1,3-dimethyl-hexahydropyrimidine-2,4,6-trione typically appears as a white or off-white powder. It is crystalline in nature.

Comment on solubility

Solubility of 5-benzyl-1,3-dimethyl-hexahydropyrimidine-2,4,6-trione

The solubility of 5-benzyl-1,3-dimethyl-hexahydropyrimidine-2,4,6-trione, a complex heterocyclic compound, is influenced by several factors, including its molecular structure and the presence of functional groups. Generally, the solubility can be summarized as follows:

  • Polarity: The polar nature of the trione functional groups enhances its solubility in polar solvents such as water and alcohols.
  • Hydrogen Bonding: The potential for hydrogen bonding with solvents can significantly affect solubility, allowing for greater interaction and dissolution.
  • Organic Solvents: It may also exhibit solubility in common organic solvents like dichloromethane and ethyl acetate due to its aromatic benzyl group.

Quantitatively, the exact solubility is often determined empirically, but it can be stated that:

  • The compound shows moderate aqueous solubility, making it accessible for various chemical reactions.
  • Solubility may be enhanced under acidic or basic conditions, depending on the pH.

In practice, it is always advisable to assess the solubility in the specific solvent of interest to predict behavior in reactions and formulations. As noted in literature, “The solubility of any compound is a gateway to its reactivity and application in diverse fields.”

Interesting facts

Interesting Facts about 5-Benzyl-1,3-dimethyl-hexahydropyrimidine-2,4,6-trione

5-Benzyl-1,3-dimethyl-hexahydropyrimidine-2,4,6-trione is a fascinating compound that belongs to the class of pyrimidines, a family known for their important roles in biology and medicine. Here are several aspects that highlight its significance:

  • Diverse Applications: Pyrimidine derivatives, including this compound, are widely studied for their potential in pharmaceuticals. They often exhibit biological activity making them ideal candidates for drug development.
  • Catalytic Properties: This compound can act as a catalyst in various chemical reactions, facilitating processes such as condensation and cyclization which are pivotal in organic synthesis.
  • Structural Complexity: The hexahydropyrimidine ring contributes to the compound’s unique properties. Its complex structure is a point of interest for chemists exploring new materials and reactions.
  • Biological Relevance: Research indicates that pyrimidine derivatives can influence various biological pathways. Understanding the effects of this specific compound could provide insights into metabolic processes.
  • Potential for Custom Synthesis: The presence of specific functional groups such as the benzyl and dimethyl moieties offers ample opportunity for synthetic chemists to create variations of this compound, possibly leading to new derivatives with enhanced properties.

In the world of chemistry, the exploration of compounds like 5-benzyl-1,3-dimethyl-hexahydropyrimidine-2,4,6-trione exemplifies the bridge between fundamental research and practical application, showcasing the endless possibilities within organic chemistry!

Synonyms
BARBITURIC ACID, 5-BENZYL-1,3-DIMETHYL-
15018-52-7
5-Benzyl-1,3-dimethylbarbituric acid
2,4,6(1H,3H,5H)-Pyrimidinetrione, 1,3-dimethyl-5-(phenylmethyl)-
RU5F9H5XHE
5-benzyl-1,3-dimethyl-1,3-diazinane-2,4,6-trione
MLS002707089
NSC-120879
NSC 120879
BRN 0225511
NSC120879
UNII-RU5F9H5XHE
5-24-09-00282 (Beilstein Handbook Reference)
SCHEMBL4435666
CHEMBL1904800
DTXSID50164484
SMR001574484
5-benzyl-1,3-dimethyl-pyrimidine-2,4,6-trione
2,6(1H,3H,5H)-Pyrimidinetrione, 1,3-dimethyl-5-(phenylmethyl)-