5-Bromo-6-chloro-2-(methylthio)pyrimidin-4-amine
95%
- Product Code: 49033
CAS:
63931-22-6
| Molecular Weight: | 254.5353 g./mol | Molecular Formula: | C₅H₅BrClN₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16988271 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure is particularly valuable in the development of kinase inhibitors, which are crucial for targeting specific pathways in diseases such as cancer. The presence of both bromo and chloro substituents allows for further functionalization, making it a versatile building block in organic synthesis. Additionally, its pyrimidine core is a common motif in drugs that interact with nucleic acids, suggesting potential applications in antiviral or antibacterial therapies. Researchers often employ this compound to explore and optimize the biological activity of new drug candidates, leveraging its reactivity to create diverse derivatives for screening and testing.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,009.00 |
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5-Bromo-6-chloro-2-(methylthio)pyrimidin-4-amine
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure is particularly valuable in the development of kinase inhibitors, which are crucial for targeting specific pathways in diseases such as cancer. The presence of both bromo and chloro substituents allows for further functionalization, making it a versatile building block in organic synthesis. Additionally, its pyrimidine core is a common motif in drugs that interact with nucleic acids, suggesting potential applications in antiviral or antibacterial therapies. Researchers often employ this compound to explore and optimize the biological activity of new drug candidates, leveraging its reactivity to create diverse derivatives for screening and testing.
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