Pyrimidine-4-carbaldehyde oxime
≥95%
- Product Code: 118873
CAS:
1073-65-0
| Molecular Weight: | 123.11 g./mol | Molecular Formula: | C₅H₅N₃O |
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| Melting Point: | Boiling Point: | 174°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
Pyrimidine-4-carbaldehyde oxime is primarily used in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various pharmaceutical compounds, particularly those targeting neurological disorders and infectious diseases. Its oxime functional group makes it valuable for creating molecules with potential therapeutic effects, such as inhibitors for specific enzymes or receptors. Additionally, it is utilized in the design of novel antiviral and antibacterial agents, leveraging its structural properties to enhance drug efficacy and selectivity. Researchers also explore its role in developing treatments for cancer, as it can be modified to interact with cellular pathways involved in tumor growth. Its versatility in chemical reactions further supports its application in creating diverse biologically active molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $38.12 |
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| 0.250 | 10-20 days | $63.54 |
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| 1.000 | 10-20 days | $190.99 |
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Pyrimidine-4-carbaldehyde oxime
Pyrimidine-4-carbaldehyde oxime is primarily used in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various pharmaceutical compounds, particularly those targeting neurological disorders and infectious diseases. Its oxime functional group makes it valuable for creating molecules with potential therapeutic effects, such as inhibitors for specific enzymes or receptors. Additionally, it is utilized in the design of novel antiviral and antibacterial agents, leveraging its structural properties to enhance drug efficacy and selectivity. Researchers also explore its role in developing treatments for cancer, as it can be modified to interact with cellular pathways involved in tumor growth. Its versatility in chemical reactions further supports its application in creating diverse biologically active molecules.
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