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CAS 10302-79-1

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3',5'-di-o-toluoyl-2-deoxy-5-azacytosine

Description:
3',5'-di-o-toluoyl-2-deoxy-5-azacytosine is a modified nucleoside derivative that features a 2-deoxy sugar moiety and an azacytosine base, where the nitrogen atom replaces the carbon atom at the 5-position of the pyrimidine ring. This compound is characterized by the presence of two o-toluoyl groups, which are aromatic acyl substituents that enhance the lipophilicity and stability of the molecule. The modifications impart unique biochemical properties, making it of interest in nucleic acid chemistry and potential applications in molecular biology and medicinal chemistry. The azacytosine moiety can participate in hydrogen bonding and base pairing, similar to natural nucleobases, while the toluoyl groups can influence the compound's solubility and interaction with biological targets. Overall, this compound exemplifies the structural diversity found in nucleoside analogs, which can be tailored for specific functions in research and therapeutic contexts.
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