N4-Benzoyl-3',5'-O-(1,1,3,3-tetraisopropyl-1,3-disiloxanediyl)cytidine
≥97%
- Product Code: 97318
CAS:
69304-43-4
| Molecular Weight: | 589.84 g./mol | Molecular Formula: | C₂₈H₄₃N₃O₇Si₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 101°C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
Primarily used in the synthesis of modified nucleosides, this compound plays a crucial role in oligonucleotide chemistry. It is particularly valuable in the protection of hydroxyl groups during the preparation of nucleoside phosphoramidites, which are essential intermediates in the automated synthesis of DNA and RNA sequences. The tetraisopropyldisiloxane (TIPDS) group provides robust protection for the 3' and 5' hydroxyl positions, ensuring selective reactivity at other sites. This chemical is also employed in the development of therapeutic oligonucleotides, including antisense oligonucleotides and siRNA, where precise chemical modifications are necessary to enhance stability, binding affinity, and cellular uptake. Its application extends to research in genetic engineering, molecular biology, and drug discovery, where controlled nucleoside modifications are critical for studying gene function and developing targeted treatments.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿3,726.00 |
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| 1.000 | 10-20 days | ฿13,896.00 |
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N4-Benzoyl-3',5'-O-(1,1,3,3-tetraisopropyl-1,3-disiloxanediyl)cytidine
Primarily used in the synthesis of modified nucleosides, this compound plays a crucial role in oligonucleotide chemistry. It is particularly valuable in the protection of hydroxyl groups during the preparation of nucleoside phosphoramidites, which are essential intermediates in the automated synthesis of DNA and RNA sequences. The tetraisopropyldisiloxane (TIPDS) group provides robust protection for the 3' and 5' hydroxyl positions, ensuring selective reactivity at other sites. This chemical is also employed in the development of therapeutic oligonucleotides, including antisense oligonucleotides and siRNA, where precise chemical modifications are necessary to enhance stability, binding affinity, and cellular uptake. Its application extends to research in genetic engineering, molecular biology, and drug discovery, where controlled nucleoside modifications are critical for studying gene function and developing targeted treatments.
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