4-Chloro-6-iodo-5-methylthieno[2,3-d]pyrimidine
97%
- Product Code: 47218
CAS:
1823372-30-0
| Molecular Weight: | 310.54 g./mol | Molecular Formula: | C₇H₄ClIN₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26517433 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an 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 both chloro and iodo substituents, makes it a versatile building block for developing potential pharmaceutical agents, particularly in the design of kinase inhibitors. These inhibitors are often explored for their therapeutic potential in treating diseases such as cancer, where they can target specific signaling pathways involved in cell proliferation and survival. Additionally, the thieno[2,3-d]pyrimidine core is known for its ability to interact with biological targets, making this compound valuable in drug discovery and optimization processes. Researchers also leverage its reactivity in cross-coupling reactions to introduce diverse functional groups, enabling the creation of complex molecules for further biological evaluation.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿24,678.00 |
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| 5.000 | 10-20 days | ฿49,356.00 |
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4-Chloro-6-iodo-5-methylthieno[2,3-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 both chloro and iodo substituents, makes it a versatile building block for developing potential pharmaceutical agents, particularly in the design of kinase inhibitors. These inhibitors are often explored for their therapeutic potential in treating diseases such as cancer, where they can target specific signaling pathways involved in cell proliferation and survival. Additionally, the thieno[2,3-d]pyrimidine core is known for its ability to interact with biological targets, making this compound valuable in drug discovery and optimization processes. Researchers also leverage its reactivity in cross-coupling reactions to introduce diverse functional groups, enabling the creation of complex molecules for further biological evaluation.
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