1,3-diallyl-5,5-diethyl-barbituric acid

Identification

Molecular formula

C₁₄H₂₂N₂O₃

CAS number

32793-63-4

IUPAC name

1,3-diallyl-5,5-diethyl-hexahydropyrimidine-2,4,6-trione

State

At room temperature, 1,3-diallyl-5,5-diethyl-barbituric acid is typically found in a crystalline solid state.

Melting point (Celsius)

118.00

Melting point (Kelvin)

391.15

Boiling point (Celsius)

312.00

Boiling point (Kelvin)

585.15

General information

Molecular weight

280.35g/mol

Molar mass

280.3530g/mol

Density

1.1562g/cm³

Appearence

The compound 1,3-diallyl-5,5-diethyl-hexahydropyrimidine-2,4,6-trione appears as a crystalline solid. Its structure indicates a series of aliphatic chains, and the unsaturated carbon-carbon double bonds contribute to its characteristic appearance. Its color can range from colorless to a pale yellow depending on purity and conditions of crystallization.

Comment on solubility

Solubility of 1,3-Diallyl-5,5-diethyl-hexahydropyrimidine-2,4,6-trione

The solubility of 1,3-diallyl-5,5-diethyl-hexahydropyrimidine-2,4,6-trione is influenced by several factors related to its molecular structure and interactions with solvents. Generally, compounds with similar polarities tend to dissolve well in each other — a concept known as "like dissolves like."

Polarity: This compound features various functional groups that can contribute to its polarity, affecting its solubility in polar solvents, such as water, as well as in nonpolar solvents.
Hydrogen Bonding: If the compound can form hydrogen bonds, it may exhibit increased solubility in polar solvents, enhancing its interactions and dissolution.
Hydrophobicity: The diethyl groups can introduce hydrophobic characteristics, potentially reducing solubility in highly polar solvents.

As a result, while the compound may display some solubility in organic solvents, its solubility profile can vary significantly based on environmental conditions and the presence of other molecules. In summary, to fully understand the solubility behavior of 1,3-diallyl-5,5-diethyl-hexahydropyrimidine-2,4,6-trione, empirical testing alongside theoretical analysis is recommended.

Interesting facts

Interesting Facts about 1,3-diallyl-5,5-diethyl-hexahydropyrimidine-2,4,6-trione

This intriguing compound, a member of the hexahydropyrimidine family, displays a fascinating structure that warrants a closer examination. Here are some captivating insights into this compound:

Structural Versatility: The presence of both diallyl and diethyl groups imparts a unique level of structural complexity, making it a subject of interest in the field of organic synthesis.
Chemical Reactivity: It is characterized by a rich array of chemical reactivity, allowing it to participate in various reactions, including cycloadditions and functional group transformations.
Potential Applications: Compounds like this may have potential applications in the development of pharmaceuticals and agrochemicals due to their unique molecular properties and functional groups.
Synthetic Pathways: The synthesis of such compounds often involves innovative strategies that highlight the creativity and adaptability of modern organic chemistry.
Research Interest: Ongoing research continues to explore the biological activity of hexahydropyrimidine derivatives, potentially uncovering new therapeutic avenues.

As one delves deeper into the world of organic chemistry, compounds like 1,3-diallyl-5,5-diethyl-hexahydropyrimidine-2,4,6-trione remind us of the intricate balance between complexity and functionality in molecular design. Such studies pave the way to innovative solutions in various scientific domains.

Synonyms

N,N'-Diallylbarbital

BARBITURIC ACID, 1,3-DIALLYL-5,5-DIETHYL-

14167-74-9

BRN 0244672

1,3-Diallyl-5,5-diethylbarbituric acid

DTXSID70161793

DTXCID4084284

5-24-09-00147 (Beilstein Handbook Reference)

5,5-diethyl-1,3-bis(prop-2-enyl)-1,3-diazinane-2,4,6-trione

1,3-Diallyl-5,5-diethylpyrimidine-2,4,6(1H,3H,5H)-trione