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Thymine Arabinoside

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Identification
Molecular formula
C9H12N2O6
CAS number
65-71-4
IUPAC name
1-(4-hydroxy-5-methyl-tetrahydrofuran-2-yl)pyrimidine-2,4-dione
State
State

At room temperature, Thymine Arabinoside is typically in a solid state.

Melting point (Celsius)
260.00
Melting point (Kelvin)
533.15
Boiling point (Celsius)
760.00
Boiling point (Kelvin)
1 033.15
General information
Molecular weight
244.21g/mol
Molar mass
244.2110g/mol
Density
1.3400g/cm3
Appearence

Thymine Arabinoside is typically a white to off-white crystalline powder.

Comment on solubility

Solubility of 1-(4-hydroxy-5-methyl-tetrahydrofuran-2-yl)pyrimidine-2,4-dione

The solubility of the compound 1-(4-hydroxy-5-methyl-tetrahydrofuran-2-yl)pyrimidine-2,4-dione (C9H12N2O6) can be characterized by several notable factors:

  • Polarity: This compound contains various functional groups, such as hydroxyl and carbonyl groups, which contribute to its polar nature. As a result, it is likely to have good solubility in polar solvents like water.
  • Hydrogen Bonding: The presence of the hydroxyl group enables the formation of hydrogen bonds with solvents, further enhancing its solubility in aqueous environments.
  • Solvent Compatibility: It may also exhibit limited solubility in non-polar solvents due to its polarity. Hence, it is typically more soluble in solvents that can engage in dipole-dipole interactions.

In conclusion, the solubility of this compound can be summarized as follows:

  • High solubility in polar solvents
  • Limited solubility in non-polar solvents

Understanding the solubility of this compound is crucial for various applications, including pharmaceutical formulation and chemical synthesis, where solvent choice can significantly impact reaction efficiency and product yield.

Interesting facts

Interesting Facts About 1-(4-hydroxy-5-methyl-tetrahydrofuran-2-yl)pyrimidine-2,4-dione

This intriguing compound, 1-(4-hydroxy-5-methyl-tetrahydrofuran-2-yl)pyrimidine-2,4-dione, is a member of the pyrimidine family, renowned for its diverse applications in medicinal chemistry. Below are some compelling insights:

  • Biological Significance: Pyrimidine derivatives are crucial in biological systems, as they serve as fundamental components of nucleotides, which are the building blocks of DNA and RNA. This compound's structure may contribute to its potential biological activity.
  • Pharmaceutical Potential: There is increasing interest in the role of such compounds in drug design and development. Their unique structures can interact with biological targets, making them candidates for therapeutic agents.
  • Structure-Activity Relationship: The variation in substituents on the pyrimidine core, such as the hydroxy and tetrahydrofuran groups, influences their biological properties. Understanding these relationships is essential for creating more effective compounds.
  • Research Applications: Compounds like this one are often investigated for their potential anti-cancer, anti-viral, and anti-inflammatory properties. Scientific studies may focus on how structural modifications enhance efficacy and reduce side effects.
  • Analytical Techniques: The characterization of such compounds typically involves advanced techniques such as NMR, mass spectrometry, and X-ray crystallography. These methods provide insights into their structure and reactivity.

In conclusion, the study of 1-(4-hydroxy-5-methyl-tetrahydrofuran-2-yl)pyrimidine-2,4-dione exemplifies the intersection between structure and function in chemistry. As research continues to unfold, the potential applications of this compound may lead to groundbreaking discoveries in the field of pharmaceuticals.

Synonyms
PD041624