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Sulfur amino acid

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Identification
Molecular formula
C12H18N6O4S
CAS number
.
IUPAC name
2-amino-4-[[5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl-methyl-lambda4-sulfanyl]butanoic acid
State
State

At room temperature, this compound exists as a solid.

Melting point (Celsius)
146.00
Melting point (Kelvin)
419.15
Boiling point (Celsius)
221.00
Boiling point (Kelvin)
494.15
General information
Molecular weight
263.21g/mol
Molar mass
263.2140g/mol
Density
1.3500g/cm3
Appearence

The compound appears as a white or off-white crystalline solid.

Comment on solubility

Solubility of 2-amino-4-[[5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl-methyl-lambda4-sulfanyl]butanoic acid

The solubility of the compound with the formula C12H18N6O4S can be characterized as follows:

  • Water Solubility: Generally, compounds containing amino and hydroxyl groups tend to exhibit good solubility in water due to hydrogen bonding interactions.
  • pH Dependence: The solubility may vary with pH; being an amino acid derivative, it might increase in acidic environments where the amino group is protonated.
  • Organic Solvents: Solubility in organic solvents can be expected to be lower, as the presence of multiple polar functional groups may restrict solvation in non-polar media.

In general, solubility can be influenced by:

  1. The molecular structure—compounds with a more polar character tend to have higher solubility in polar solvents.
  2. The presence of functional groups like -NH2 and -OH, which can participate in solvation.
  3. Temperature—the solubility often increases with a rise in temperature.

In conclusion, while we anticipate reasonable water solubility for this compound based on its structural features, the specific solubility must be experimentally determined to provide accurate data. Understanding these solubility characteristics is crucial for potential applications in pharmaceutical and chemical industries.

Interesting facts

Exploring the Intricacies of 2-amino-4-[[5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl-methyl-lambda4-sulfanyl]butanoic acid

The compound 2-amino-4-[[5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl-methyl-lambda4-sulfanyl]butanoic acid is a fascinating example of the intricate world of organic chemistry. This compound serves as a valuable target in the study of medicinal and pharmaceutical chemistry due to its structural complexity and potential biological activities.

Key Features

  • Multi-functional structure: The presence of multiple functional groups, including amino, hydroxyl, and sulfanyl, suggests a diverse range of reactivity and interactions.
  • Connections to purines: The incorporation of the 6-aminopurine moiety highlights its potential relevance in nucleic acid chemistry, possibly influencing DNA and RNA interactions.
  • Compatibility in bioactivity: Compounds with similar frameworks have been explored for therapeutic applications, particularly in the fields of antiviral and anticancer agents.

This compound exemplifies the intricate relationship between structure and function in chemical compounds. The design and modification of such complex molecules not only expand our knowledge of organic synthesis but also underline the myriad possibilities for drug discovery and development. Furthermore, the potential for innovative medicinal applications warrants further investigation. As a student or scientist, exploring compounds like this can inspire new ideas and approaches in both research and practical applications.

In conclusion, 2-amino-4-[[5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl-methyl-lambda4-sulfanyl]butanoic acid represents a unique intersection of chemistry and biology, exemplifying how detailed molecular design can lead to significant advancements in health and medicine.