(2R,3R,4R,5R)-5-(6-Benzamido-9H-purin-9-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-fluorotetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite
>97%
- Product Code: 97099
CAS:
136834-22-5
| Molecular Weight: | 875.92 g./mol | Molecular Formula: | C₄₇H₅₁FN₇O₇P |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
This compound is primarily used in the synthesis of oligonucleotides, particularly in the field of molecular biology and genetic research. It serves as a key building block in the solid-phase synthesis of DNA and RNA sequences, enabling the creation of customized strands for applications such as gene editing, PCR, and sequencing. The protective groups, such as the bis(4-methoxyphenyl)(phenyl)methyl (DMT) group, ensure selective reactivity during the synthesis process, while the phosphoramidite moiety allows for efficient coupling with other nucleotides. Its fluorinated structure enhances stability and precision in the assembly of nucleic acids, making it valuable for advanced genetic studies and therapeutic development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $59.41 |
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| 0.250 | 10-20 days | $90.19 |
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| 1.000 | 10-20 days | $233.30 |
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(2R,3R,4R,5R)-5-(6-Benzamido-9H-purin-9-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-fluorotetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite
This compound is primarily used in the synthesis of oligonucleotides, particularly in the field of molecular biology and genetic research. It serves as a key building block in the solid-phase synthesis of DNA and RNA sequences, enabling the creation of customized strands for applications such as gene editing, PCR, and sequencing. The protective groups, such as the bis(4-methoxyphenyl)(phenyl)methyl (DMT) group, ensure selective reactivity during the synthesis process, while the phosphoramidite moiety allows for efficient coupling with other nucleotides. Its fluorinated structure enhances stability and precision in the assembly of nucleic acids, making it valuable for advanced genetic studies and therapeutic development.
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