5-Fluoro-2'-deoxycytidine
98%
- Product Code: 110619
Alias:
5-fluorodeoxycytidine
CAS:
10356-76-0
| Molecular Weight: | 245.21 g./mol | Molecular Formula: | C₉H₁₂FN₃O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00077348 | |
| Melting Point: | 196 °C | Boiling Point: | 465℃ |
| Density: | 1.82 | Storage Condition: | room temperature |
Product Description:
Used primarily in biochemical research, this compound serves as a nucleoside analog. It plays a crucial role in studying DNA synthesis and repair mechanisms. Researchers utilize it to investigate the incorporation of modified nucleotides into DNA, which helps in understanding cellular processes and the effects of genetic mutations. Additionally, it is employed in the development of antiviral and anticancer therapies, where it acts to inhibit the replication of certain viruses and cancer cells by disrupting their DNA synthesis. Its application extends to molecular biology techniques, including polymerase chain reaction (PCR), where it aids in the study of DNA replication fidelity and enzyme kinetics.
Product Specification:
| Test | Specification |
|---|---|
| Purity (HPLC) | 98-100 |
| Specific Rotation [A]20/D(C=1,H2O) | 65 Degree Celsius - 75 Degree Celsius |
| Appearance | White To Off-White Powder |
| Infrared Spectrometry | Conforms To Structure |
| Solubility | >20 MG/ML In DMSO |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,860.00 |
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| 1.000 | 10-20 days | ฿7,150.00 |
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5-Fluoro-2'-deoxycytidine
Used primarily in biochemical research, this compound serves as a nucleoside analog. It plays a crucial role in studying DNA synthesis and repair mechanisms. Researchers utilize it to investigate the incorporation of modified nucleotides into DNA, which helps in understanding cellular processes and the effects of genetic mutations. Additionally, it is employed in the development of antiviral and anticancer therapies, where it acts to inhibit the replication of certain viruses and cancer cells by disrupting their DNA synthesis. Its application extends to molecular biology techniques, including polymerase chain reaction (PCR), where it aids in the study of DNA replication fidelity and enzyme kinetics.
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