6-Amino-1-benzyl-3-methylpyrimidine-2,4(1H,3H)-dione
≥95%
- Product Code: 120492
CAS:
53681-51-9
| Molecular Weight: | 231.25 g./mol | Molecular Formula: | C₁₂H₁₃N₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03480188 | |
| Melting Point: | Boiling Point: | 375.3°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. It plays a significant role in the development of drugs targeting neurological disorders, particularly those involving the modulation of neurotransmitter systems. Additionally, it is employed in the creation of compounds with potential anti-inflammatory and analgesic properties, making it valuable for pain management research. Its structural framework is also explored in the design of molecules with antimicrobial activity, contributing to the development of new antibiotics. Researchers leverage its pyrimidine core to investigate its interactions with biological targets, aiding in the discovery of novel therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,260.00 |
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| 0.250 | 10-20 days | ฿2,097.00 |
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| 1.000 | 10-20 days | ฿5,661.00 |
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6-Amino-1-benzyl-3-methylpyrimidine-2,4(1H,3H)-dione
This chemical is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. It plays a significant role in the development of drugs targeting neurological disorders, particularly those involving the modulation of neurotransmitter systems. Additionally, it is employed in the creation of compounds with potential anti-inflammatory and analgesic properties, making it valuable for pain management research. Its structural framework is also explored in the design of molecules with antimicrobial activity, contributing to the development of new antibiotics. Researchers leverage its pyrimidine core to investigate its interactions with biological targets, aiding in the discovery of novel therapeutic agents.
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