3'-5'-Di-O-acetyl-2'-deoxyinosine is a modified nucleoside that features an inosine base attached to a deoxyribose sugar, with acetyl groups at the 3' and 5' positions. This compound is characterized by its structural modifications, which enhance its stability and solubility compared to unmodified nucleosides. The presence of acetyl groups can influence its reactivity and interactions with enzymes, making it useful in biochemical applications, particularly in the synthesis of oligonucleotides and as a potential building block in nucleic acid research. Its molecular structure allows for participation in various biochemical pathways, and it may exhibit unique biological activities due to its modifications. Additionally, the compound's CAS number, 106568-79-0, serves as a unique identifier for regulatory and research purposes. Overall, 3'-5'-Di-O-acetyl-2'-deoxyinosine is significant in the field of nucleic acid chemistry, contributing to advancements in molecular biology and therapeutic development.

3'-5'-DI-O-ACETYL-2'-DEOXYINOSINE

106568-79-0: 3'-5'-Di-O-acetyl-2'-deoxyinosine is a modified nucleoside that features an inosine base attached to a deoxyribose sugar, with acetyl groups at the 3' and 5' positions. This compound is characterized by its structural modifications, which enhance its stability and solubility compared to unmodified nucleosides. The presence of acetyl groups can influence its reactivity and interactions with enzymes, making it useful in biochemical applications, particularly in the synthesis of oligonucleotides and as a potential building block in nucleic acid research. Its molecular structure allows for participation in various biochemical pathways, and it may exhibit unique biological activities due to its modifications. Additionally, the compound's CAS number, 106568-79-0, serves as a unique identifier for regulatory and research purposes. Overall, 3'-5'-Di-O-acetyl-2'-deoxyinosine is significant in the field of nucleic acid chemistry, contributing to advancements in molecular biology and therapeutic development.

<p>3',5'-Di-O-acetyl-2'-deoxyinosine is a dimer of 2'-deoxyinosine, which is an analog of inosine. It catalyzes the chlorination of aromatic substrates such as benzene or toluene with chlorine gas in the presence of FeCl3. The resulting product is a chlorinated aromatic compound. This reaction proceeds by electrophilic substitution at the C-2 position. 3',5'-Di-O-acetyl-2'-deoxyinosine has been shown to be more active than 2'-deoxyinosine in this reaction because it reacts faster and its reactive intermediate is more stable.</p>

CAS 106568-79-0

3'-5'-DI-O-ACETYL-2'-DEOXYINOSINE

3',5'-Di-O-acetyl-2'-deoxyinosine

Ref: 3D-GEA56879