The compound $name$ ((2R,3S,4R,5R)-5-(6-Amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl 4-methylbenzenesulfonate is commonly utilized in chemical synthesis as a protecting group for nucleosides or nucleotides. This compound serves as a versatile tool in organic chemistry for selectively blocking specific functional groups within these biomolecules, allowing for controlled reactions to take place without unwanted side reactions. Through strategic placement and subsequent removal of this protecting group, chemists can precisely manipulate the reactivity of the nucleoside or nucleotide, leading to the synthesis of complex structures with high precision. Due to its efficiency and reliability in safeguarding key functional groups, the application of $name$ has become fundamental in the synthesis of various pharmaceuticals, nucleic acid analogs, and other bioactive compounds.
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