N6-Benzoyl-2'-O-tert-butyldimethylsilyl-5'-O-DMT-adenosine, 10 g

This nucleotide's highly pure composition ensures reliable results in various laboratory settings. Its chemical structure enables precise control over reactions and interactions.

How the Formula Works

This compound's synthesis involves the attachment of tert-butyldimethylsilyl group to the 2'-hydroxyl position of adenosine, resulting in a stable and water-soluble derivative. The presence of the N6-benzoyl group enhances its solubility and reactivity in organic solvents.

Product Use Cases

• Enhances reaction rates and yields in organic and biochemical transformations.
• Facilitates the study of adenosine derivatives' pharmacological properties.
• Suitable for small-scale production runs due to its 10 G packaging.
• May be used in the development of new therapeutic agents or diagnostic tools.
• Can be employed in the creation of complex molecular structures through controlled modifications.