9-Pentofuranosyl-2-(trifluoromethyl)-9H-purin-6-amine, with the CAS number 4627-40-1, is a purine derivative characterized by its unique structural features. This compound contains a purine base, which is a fundamental component of nucleic acids, and is modified with a pentofuranosyl sugar moiety, enhancing its biological relevance. The presence of a trifluoromethyl group at the 2-position of the purine ring significantly influences its chemical properties, potentially enhancing lipophilicity and altering its interaction with biological targets. The amine group at the 6-position contributes to its reactivity and solubility in various solvents. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry and drug development. Its stability, solubility, and reactivity can vary based on environmental conditions, such as pH and temperature, which are crucial for its application in biological systems. Overall, this compound represents a fascinating intersection of organic chemistry and biochemistry, with potential implications in therapeutic research.

9-pentofuranosyl-2-(trifluoromethyl)-9H-purin-6-amine

4627-40-1: 9-Pentofuranosyl-2-(trifluoromethyl)-9H-purin-6-amine, with the CAS number 4627-40-1, is a purine derivative characterized by its unique structural features. This compound contains a purine base, which is a fundamental component of nucleic acids, and is modified with a pentofuranosyl sugar moiety, enhancing its biological relevance. The presence of a trifluoromethyl group at the 2-position of the purine ring significantly influences its chemical properties, potentially enhancing lipophilicity and altering its interaction with biological targets. The amine group at the 6-position contributes to its reactivity and solubility in various solvents. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry and drug development. Its stability, solubility, and reactivity can vary based on environmental conditions, such as pH and temperature, which are crucial for its application in biological systems. Overall, this compound represents a fascinating intersection of organic chemistry and biochemistry, with potential implications in therapeutic research.

<p>Nucleoside Derivatives –8-substituted purine nucleosides ;ara-nucleosides.</p>

CAS 4627-40-1

9-pentofuranosyl-2-(trifluoromethyl)-9H-purin-6-amine

2-Trifluoromethyl adenosine

Ref: TM-TNU0327