3'-Deoxy-5'-O-(dimethoxytrityl)-5-methyluridine is a modified nucleoside that plays a significant role in nucleic acid chemistry and molecular biology. This compound features a uridine base, which is a pyrimidine nucleoside, with specific modifications that enhance its stability and solubility. The presence of the dimethoxytrityl (DMT) group at the 5' position provides protection against nucleophilic attack, making it useful in oligonucleotide synthesis. The 3'-deoxy modification indicates the absence of a hydroxyl group at the 3' position, which further contributes to its stability and prevents unwanted reactions during synthesis. The methyl group at the 5 position of the uridine base can influence the compound's binding affinity and biological activity. Overall, this compound is valuable in the development of therapeutic oligonucleotides and in various applications in genetic research, including RNA synthesis and modification. Its unique structural features make it a key component in the design of nucleic acid-based technologies.

3'-DEOXY-5'-O-(DIMETHOXYTRITYL)-5-METHYLURIDINE

114551-15-4: 3'-Deoxy-5'-O-(dimethoxytrityl)-5-methyluridine is a modified nucleoside that plays a significant role in nucleic acid chemistry and molecular biology. This compound features a uridine base, which is a pyrimidine nucleoside, with specific modifications that enhance its stability and solubility. The presence of the dimethoxytrityl (DMT) group at the 5' position provides protection against nucleophilic attack, making it useful in oligonucleotide synthesis. The 3'-deoxy modification indicates the absence of a hydroxyl group at the 3' position, which further contributes to its stability and prevents unwanted reactions during synthesis. The methyl group at the 5 position of the uridine base can influence the compound's binding affinity and biological activity. Overall, this compound is valuable in the development of therapeutic oligonucleotides and in various applications in genetic research, including RNA synthesis and modification. Its unique structural features make it a key component in the design of nucleic acid-based technologies.

CAS 114551-15-4

3'-DEOXY-5'-O-(DIMETHOXYTRITYL)-5-METHYLURIDINE

2,4(1H,3H)-Pyrimidinedione, 1-[5-O-[bis(4-methoxyphenyl)phenylmethyl]-3-deoxy-β-D-threo-pentofuranosyl]-5-methyl-

Ref: IN-DA000EOF