(2R,3R,4S,5R)-2-(6-Amino-2-fluoro-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
98%
- Product Code: 79188
CAS:
146-78-1
| Molecular Weight: | 285.23 g./mol | Molecular Formula: | C₁₀H₁₂FN₅O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 240°C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of biochemistry and molecular biology as a modified nucleoside. It serves as a crucial component in the synthesis of oligonucleotides, particularly in the development of probes and primers for nucleic acid detection and amplification techniques like PCR. Its fluorinated structure enhances the stability and binding affinity of the synthesized oligonucleotides, making it valuable for diagnostic applications and research studies targeting specific genetic sequences. Additionally, it is employed in the study of enzyme mechanisms and nucleic acid interactions, providing insights into the biochemical pathways and functions of nucleic acids.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿910.00 |
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| 1.000 | 10-20 days | ฿2,600.00 |
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(2R,3R,4S,5R)-2-(6-Amino-2-fluoro-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
This compound is primarily utilized in the field of biochemistry and molecular biology as a modified nucleoside. It serves as a crucial component in the synthesis of oligonucleotides, particularly in the development of probes and primers for nucleic acid detection and amplification techniques like PCR. Its fluorinated structure enhances the stability and binding affinity of the synthesized oligonucleotides, making it valuable for diagnostic applications and research studies targeting specific genetic sequences. Additionally, it is employed in the study of enzyme mechanisms and nucleic acid interactions, providing insights into the biochemical pathways and functions of nucleic acids.
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