1-((1R,3R,4R,7S)-1-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-3-yl)-5-methylpyrimidine-2,4(1H,3H)-dione
95%
- Product Code: 82157
CAS:
206055-71-2
| Molecular Weight: | 572.61 g./mol | Molecular Formula: | C₃₂H₃₂N₂O₈ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31537291 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.331±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of nucleic acid chemistry, particularly in the synthesis of oligonucleotides. It serves as a protected nucleoside derivative, where the hydroxyl groups are shielded to prevent unwanted reactions during the synthesis process. The bis(4-methoxyphenyl)(phenyl)methoxy (DMT) group acts as a protecting group for the 5'-hydroxyl, enabling selective deprotection and subsequent coupling in solid-phase oligonucleotide synthesis. This compound is especially valuable in the preparation of modified nucleosides, which are essential for studying DNA/RNA interactions, developing therapeutic oligonucleotides, and creating probes for molecular biology applications. Its structural features ensure stability and controlled reactivity, making it a key intermediate in the production of custom oligonucleotides for research and pharmaceutical purposes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿30,420.00 |
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1-((1R,3R,4R,7S)-1-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-3-yl)-5-methylpyrimidine-2,4(1H,3H)-dione
This compound is primarily utilized in the field of nucleic acid chemistry, particularly in the synthesis of oligonucleotides. It serves as a protected nucleoside derivative, where the hydroxyl groups are shielded to prevent unwanted reactions during the synthesis process. The bis(4-methoxyphenyl)(phenyl)methoxy (DMT) group acts as a protecting group for the 5'-hydroxyl, enabling selective deprotection and subsequent coupling in solid-phase oligonucleotide synthesis. This compound is especially valuable in the preparation of modified nucleosides, which are essential for studying DNA/RNA interactions, developing therapeutic oligonucleotides, and creating probes for molecular biology applications. Its structural features ensure stability and controlled reactivity, making it a key intermediate in the production of custom oligonucleotides for research and pharmaceutical purposes.
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