2-Chloro-4-(3-nitrophenoxy)thieno[3,2-d]pyrimidine
97%
- Product Code: 73966
CAS:
1353553-07-7
| Molecular Weight: | 307.71 g./mol | Molecular Formula: | C₁₂H₆ClN₃O₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30185158 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a thieno[3,2-d]pyrimidine core, makes it a valuable scaffold for developing potential therapeutic agents, particularly in the design of kinase inhibitors. Kinase inhibitors are crucial in targeting specific signaling pathways involved in diseases such as cancer, inflammation, and autoimmune disorders. Additionally, the presence of the nitro and chloro substituents allows for further chemical modifications, enabling the creation of diverse derivatives with enhanced pharmacological properties. Researchers often explore its potential in drug discovery programs aimed at identifying novel compounds with improved efficacy and selectivity for specific biological targets.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to light-yellow solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿680.00 |
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| 0.250 | 10-20 days | ฿1,020.00 |
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2-Chloro-4-(3-nitrophenoxy)thieno[3,2-d]pyrimidine
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a thieno[3,2-d]pyrimidine core, makes it a valuable scaffold for developing potential therapeutic agents, particularly in the design of kinase inhibitors. Kinase inhibitors are crucial in targeting specific signaling pathways involved in diseases such as cancer, inflammation, and autoimmune disorders. Additionally, the presence of the nitro and chloro substituents allows for further chemical modifications, enabling the creation of diverse derivatives with enhanced pharmacological properties. Researchers often explore its potential in drug discovery programs aimed at identifying novel compounds with improved efficacy and selectivity for specific biological targets.
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