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Adenosine

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Identification
Molecular formula
C10H13N5O4
CAS number
58-61-7
IUPAC name
2-(2-aminoethylsulfanylmethyl)-5-(6-aminopurin-9-yl)tetrahydrofuran-3,4-diol
State
State

At room temperature, adenosine is in a solid state, typically appearing as a crystalline powder as previously mentioned.

Melting point (Celsius)
234.00
Melting point (Kelvin)
507.15
Boiling point (Celsius)
354.00
Boiling point (Kelvin)
627.15
General information
Molecular weight
267.24g/mol
Molar mass
267.2420g/mol
Density
1.9300g/cm3
Appearence

Adenosine typically appears as a white, crystalline powder. This compound is odorless and has a slightly bitter taste.

Comment on solubility

Solubility of 2-(2-aminoethylsulfanylmethyl)-5-(6-aminopurin-9-yl)tetrahydrofuran-3,4-diol (C10H13N5O4)

The solubility of a compound can greatly influence its applications and effectiveness, especially in pharmaceutical contexts. For the compound 2-(2-aminoethylsulfanylmethyl)-5-(6-aminopurin-9-yl)tetrahydrofuran-3,4-diol, the solubility profile is particularly intriguing due to its complex structure. Here are some notable aspects:

  • Polarity: The presence of multiple functional groups, including amines and hydroxyls, contributes to its polarity. This often results in a greater solubility in polar solvents, such as water.
  • Hydrogen Bonding: The hydroxyl groups can act as both hydrogen bond donors and acceptors, enhancing solubility in aqueous environments.
  • Amine Functionalities: The amino groups can facilitate interactions with water molecules, likely improving solubility.
  • Overall Solubility: While definitive quantitative solubility data may not be readily available, it is plausible to deduce that this compound exhibits moderate to high solubility in polar solvents.

As with many compounds featuring intricate structures, empirical testing is essential to ascertain precise solubility values. Overall, the combination of hydrophilic groups suggests that this compound is likely to be soluble to a significant extent in water and other polar solvents.

Interesting facts

Interesting Facts about 2-(2-aminoethylsulfanylmethyl)-5-(6-aminopurin-9-yl)tetrahydrofuran-3,4-diol

This compound, a unique molecule in the world of organic chemistry, exhibits fascinating structural and functional characteristics that contribute to its significance in various fields, such as pharmacology and biochemistry. Below are some intriguing points to consider:

  • Structural Complexity: The compound features a tetrahydrofuran ring, which is a five-membered cyclic ether. This structural element is crucial for its biological activity, showcasing the importance of ring systems in chemical reactivity.
  • Amino Group Importance: The presence of amino groups (–NH2) at various locations plays a vital role in the compound's reactivity and its ability to form hydrogen bonds, which can enhance biological interactions. These groups can also influence the compound's solubility and stability.
  • Biological Relevance: Compounds like these often have connections to nucleotides and nucleic acids, highlighting their potential applications in drug design and development. They may serve as *building blocks* or *modulators* for biological systems.
  • Redox Properties: The functionality of this compound could enable it to participate in redox reactions, making it an interesting subject for studies related to antioxidants and cellular protection mechanisms.
  • Research Potential: Ongoing studies may reveal how such compounds can impact cellular processes, particularly those involving *nucleotide metabolism* and *DNA repair mechanisms*, which are critical areas in cancer research.

In conclusion, 2-(2-aminoethylsulfanylmethyl)-5-(6-aminopurin-9-yl)tetrahydrofuran-3,4-diol exemplifies the intricate interplay between structure and function in organic compounds. As research progresses, this compound could unveil new pathways for medicinal applications and deepen our understanding of biochemical interactions.

Synonyms
SCHEMBL14174635