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Ralitoline

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Identification
Molecular formula
C14H16N2O2S
CAS number
123456-78-9
IUPAC name
5-allyl-5-(cyclohexen-1-yl)-2-sulfanyl-1H-pyrimidine-4,6-dione
State
State

At room temperature, Ralitoline is typically in a solid state. It is stable under normal storage conditions but should be handled with care to avoid degradation.

Melting point (Celsius)
245.00
Melting point (Kelvin)
518.15
Boiling point (Celsius)
682.15
Boiling point (Kelvin)
955.30
General information
Molecular weight
324.42g/mol
Molar mass
324.4190g/mol
Density
1.4123g/cm3
Appearence

Ralitoline typically appears as an off-white to pale yellow crystalline solid. It is known for its fine and uniform crystals, offering a distinct appearance typical of many pyrimidine derivatives.

Comment on solubility

Solubility of 5-allyl-5-(cyclohexen-1-yl)-2-sulfanyl-1H-pyrimidine-4,6-dione

The solubility of 5-allyl-5-(cyclohexen-1-yl)-2-sulfanyl-1H-pyrimidine-4,6-dione can be understood through several important factors:

  • Polarity: The presence of both the sulfanyl (-SH) group and the pyrimidine ring contributes to the compound's polarity, which often influences how well it dissolves in different solvents.
  • Solvent Interaction: Polar solvents like water may interact more readily with the polar functional groups, whereas non-polar solvents, such as hexane, may not effectively solvate the compound.
  • Hydrogen Bonding: The potential for hydrogen bonding due to the sulfanyl group can enhance solubility in polar solvents, although steric hindrance from the bulky cyclohexenyl group could reduce overall solubility.
  • Temperature Effects: As with many compounds, solubility can be temperature-dependent. Typically, an increase in temperature can lead to greater solubility of organic compounds.

It is noteworthy that the specific solubility behavior of this compound requires empirical data for precise characterization, as theoretical knowledge alone cannot fully predict actual solubility in various mediums. Thus, experimental methods such as solubility tests in multiple solvents would yield the most reliable information.

Interesting facts

Interesting Facts about 5-allyl-5-(cyclohexen-1-yl)-2-sulfanyl-1H-pyrimidine-4,6-dione

The compound 5-allyl-5-(cyclohexen-1-yl)-2-sulfanyl-1H-pyrimidine-4,6-dione is a fascinating example of a heterocyclic compound that showcases the rich chemistry of pyrimidines. Pyrimidines are known for their role in various biological systems, particularly in the structure of nucleic acids like DNA and RNA. Here are some intriguing insights into this compound:

  • Structural Complexity: The presence of multiple functional groups in this compound, including an allyl group and a cyclohexenyl ring, adds a layer of structural diversity that can influence its reactivity and potential applications.
  • Biological Relevance: Many compounds related to pyrimidines exhibit significant biological activities, including antimicrobial and anticancer properties. This suggests that 5-allyl-5-(cyclohexen-1-yl)-2-sulfanyl-1H-pyrimidine-4,6-dione could be a candidate for further pharmacological studies.
  • Synthetic Interest: The ability to synthesize compounds like this one can provide chemists with valuable insights into reaction mechanisms and the design of novel organic materials.
  • Versatile Reactions: Given its unique functional groups, this compound may participate in various chemical reactions, potentially leading to the creation of new materials or therapeutic agents.

As we explore the world of organic chemistry, compounds like 5-allyl-5-(cyclohexen-1-yl)-2-sulfanyl-1H-pyrimidine-4,6-dione serve as reminders of the intricate connections between structure, function, and potential applications in medicine and materials science. The journey of understanding compounds like these is both challenging and rewarding, reflecting the beauty of scientific discovery.