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- Molecular formula
- C10H13N5O4
- CAS Number
- 5536-17-4
- IUPAC Name
- 2-(6-aminopurin-9-yl)-5-methyl-tetrahydrofuran-3,4-diol
- Molecular Weight
- 267.27g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 2.0200g/cm3
- Synonyms
- 72-90-2
Identification
Interesting facts
Discovering 2-(6-aminopurin-9-yl)-5-methyl-tetrahydrofuran-3,4-diol
This intriguing compound, known as 2-(6-aminopurin-9-yl)-5-methyl-tetrahydrofuran-3,4-diol, represents a unique intersection of organic chemistry and biochemistry. With its structure featuring both the purine base and a tetrahydrofuran ring, it stands out for several reasons:
- Biological Relevance: The compound's purine base, derived from nucleobases like adenine and guanine, places it firmly within the scope of molecular biology. Purines are critical components of DNA and RNA, and their derivatives often play essential roles in physiological processes.
- Potential Therapeutic Applications: Research has suggested that similar compounds may exhibit antiviral and anticancer activities. Chemists are actively exploring the medicinal potential of modified purines.
- Versatile Synthetic Pathways: The preparation of this compound involves intriguing synthesis methods that showcase the creativity and skill of chemists. The ability to manipulate the tetrahydrofuran unit enhances possibilities for developing new derivatives with tailored properties.
- Intramolecular Interactions: The unique structure also opens avenues for studying the interactions within the compound itself or with other biomolecules, providing insight into its stability and reactivity.
In the words of a renowned chemist, "The beauty of chemistry lies not just in the compounds themselves but in the intricate dance of atoms and molecules that dictate their function." Exploring compounds like 2-(6-aminopurin-9-yl)-5-methyl-tetrahydrofuran-3,4-diol exemplifies this principle, inviting future researchers to unlock its secrets and applications.