2-Deoxy-2,2-difluoro-D-erythro-pentonic acid γ-Lactone 3,5-dibenzoate
98%
- Product Code: 64197
CAS:
122111-01-7
| Molecular Weight: | 376.31 g./mol | Molecular Formula: | C₁₉H₁₄F₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08458308 | |
| Melting Point: | 117-119 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | -20°C |
Product Description:
This compound is primarily utilized in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. Its structure allows it to act as a key intermediate in the production of gemcitabine, a widely used chemotherapy agent. The difluoro substitution enhances the metabolic stability and biological activity of the resulting nucleoside analogs, making it valuable in medicinal chemistry. Additionally, its dibenzoate groups provide protection during synthetic processes, ensuring precise modifications to the molecule. This chemical plays a significant role in advancing pharmaceutical research, particularly in the design of targeted therapies for treating various diseases.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 121 125? |
| PURITY HPLC | 98 100% |
| SPECIFIC ROTATION 20DC1CH3CN | 69-73 |
| NFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿290.00 |
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| 5.000 | 10-20 days | ฿380.00 |
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| 25.000 | 10-20 days | ฿1,100.00 |
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| 100.000 | 10-20 days | ฿4,110.00 |
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2-Deoxy-2,2-difluoro-D-erythro-pentonic acid γ-Lactone 3,5-dibenzoate
This compound is primarily utilized in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. Its structure allows it to act as a key intermediate in the production of gemcitabine, a widely used chemotherapy agent. The difluoro substitution enhances the metabolic stability and biological activity of the resulting nucleoside analogs, making it valuable in medicinal chemistry. Additionally, its dibenzoate groups provide protection during synthetic processes, ensuring precise modifications to the molecule. This chemical plays a significant role in advancing pharmaceutical research, particularly in the design of targeted therapies for treating various diseases.
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