2-[[4-[2-(tert-Butoxycarbonyl)ethyl]phenylethyl]amino]2′,3′-O-isopropylideneadenosine-5′-N-ethylcarboxamide (CAS 120225-76-5)

2-[[4-[2-(tert-Butoxycarbonyl)ethyl]phenylethyl]amino]2′,3′-O-isopropylideneadenosine-5′-N-ethylcarboxamide, a complex compound, has garnered considerable attention in biochemical research due to its multifaceted applications in nucleic acid chemistry and nucleotide modification studies. Its complex structure comprises an adenine nucleobase coupled with an isopropylidene moiety and an N-ethylcarboxamide group, along with a phenylethylamine-derived side chain. This chemical serves as a versatile tool for investigating nucleotide modifications and developing novel methodologies for nucleic acid manipulation. In research, it has been utilized in the synthesis of modified nucleotides and nucleic acid analogs, particularly for introducing bulky or hydrophobic functionalities into RNA or DNA molecules. Moreover, 2-[[4-[2-(tert-Butoxycarbonyl)ethyl]phenylethyl]amino]2′,3′-O-isopropylideneadenosine-5′-N-ethylcarboxamide has facilitated the study of RNA structure-function relationships, RNA-protein interactions, and ribozyme catalysis. Its applications extend to the development of modified oligonucleotides for gene regulation, RNA interference, and antisense technologies. Additionally, this compound has been instrumental in elucidating the role of modified nucleotides in biological processes such as translation, RNA splicing, and RNA editing. Overall, its versatility and utility make it a valuable asset in advancing our understanding of nucleic acid biochemistry and RNA-based technologies.