N2-Phenoxyacetyl-3',5'-O-(1,1,3,3-tetraisopropyl-1,3-disiloxanediyl)guanosine
95%
- Product Code: 51651
CAS:
131474-72-1
| Molecular Weight: | 659.88 g./mol | Molecular Formula: | C₃₀H₄₅N₅O₈Si₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27976862 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.32±0.1 g/cm3(Predicted) | Storage Condition: | 2-8℃ |
Product Description:
This chemical is primarily utilized in the field of nucleotide chemistry and oligonucleotide synthesis. It serves as a protected guanosine derivative, where the phenoxyacetyl group safeguards the exocyclic amine, and the tetraisopropyldisiloxane (TIPDS) group protects the 3' and 5' hydroxyls. This protection is crucial during the stepwise construction of oligonucleotides, particularly in solid-phase synthesis, ensuring selective reactivity and preventing unwanted side reactions. The compound is especially valuable in the synthesis of modified oligonucleotides for research applications, such as the development of antisense oligonucleotides, siRNAs, and other therapeutic nucleic acids. Its use enhances the efficiency and precision of nucleotide assembly, making it a key reagent in molecular biology and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | ฿1,692.00 |
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| 0.050 | 10-20 days | ฿6,480.00 |
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N2-Phenoxyacetyl-3',5'-O-(1,1,3,3-tetraisopropyl-1,3-disiloxanediyl)guanosine
This chemical is primarily utilized in the field of nucleotide chemistry and oligonucleotide synthesis. It serves as a protected guanosine derivative, where the phenoxyacetyl group safeguards the exocyclic amine, and the tetraisopropyldisiloxane (TIPDS) group protects the 3' and 5' hydroxyls. This protection is crucial during the stepwise construction of oligonucleotides, particularly in solid-phase synthesis, ensuring selective reactivity and preventing unwanted side reactions. The compound is especially valuable in the synthesis of modified oligonucleotides for research applications, such as the development of antisense oligonucleotides, siRNAs, and other therapeutic nucleic acids. Its use enhances the efficiency and precision of nucleotide assembly, making it a key reagent in molecular biology and drug discovery.
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