(2R)-1-(6-Amino-9H-purin-9-yl)-2-propanol(CAS: 14047-28-0)

This compound, with the CAS number 14047-28-0, is a nucleoside analog characterized by its chemical structure featuring a purine ring substituted with an amino group at position 6, connected to a 2-propanol moiety. It is a white solid with high water solubility and is commonly used in pharmaceutical research for its potential biological activity. Its molecular formula is C8H12N5O, and it exhibits specific stereochemistry due to the (2R) configuration.

The compound is primarily utilized in pharmaceutical applications, such as the development of antiviral and antitumor drugs, due to its structural similarity to nucleosides. It serves as a key intermediate in research related to nucleic acid metabolism and is also employed in the synthesis of other bioactive compounds. Its versatility makes it valuable in medicinal chemistry and biochemical studies.

Safety data for this compound indicates it is generally low in toxicity when handled properly. However, standard laboratory precautions, such as wearing gloves, goggles, and a lab coat, are recommended to avoid skin or eye contact. It is advisable to consult its safety data sheet (SDS) for detailed toxicity information and regulatory guidelines, especially in industrial or research settings.

This compound should be stored in a cool, dry place, away from light, in a sealed container to maintain stability. It is recommended to keep it at temperatures below 25°C and ensure humidity levels are controlled to prevent degradation. Storage under an inert atmosphere may also be necessary, and adherence to specific container requirements is essential for long-term preservation.