3-Benzoylpyrimidine-2,4(1H,3H)-dione
95%
- Product Code: 60972
CAS:
2775-87-3
| Molecular Weight: | 216.19 g./mol | Molecular Formula: | C₁₁H₈N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00525660 | |
| Melting Point: | 214-217 °C | Boiling Point: | |
| Density: | 1.378±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceutical agents. Its structure is particularly valuable in the development of compounds with potential biological activity, such as inhibitors for specific enzymes or receptors. Additionally, it is employed in research settings to study its reactivity and potential applications in medicinal chemistry. The compound's unique pyrimidine core makes it a versatile building block for constructing more complex molecules, often targeting therapeutic areas like anti-inflammatory, anti-cancer, or anti-viral treatments. Its role in synthesizing novel drug candidates highlights its importance in advancing drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,455.00 |
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| 0.250 | 10-20 days | ฿8,100.00 |
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| 1.000 | 10-20 days | ฿16,200.00 |
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3-Benzoylpyrimidine-2,4(1H,3H)-dione
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceutical agents. Its structure is particularly valuable in the development of compounds with potential biological activity, such as inhibitors for specific enzymes or receptors. Additionally, it is employed in research settings to study its reactivity and potential applications in medicinal chemistry. The compound's unique pyrimidine core makes it a versatile building block for constructing more complex molecules, often targeting therapeutic areas like anti-inflammatory, anti-cancer, or anti-viral treatments. Its role in synthesizing novel drug candidates highlights its importance in advancing drug discovery and development.
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