4-(5-Bromo-1H-indol-3-yl)pyrimidin-2-amine
97%
- Product Code: 46361
CAS:
213473-00-8
| Molecular Weight: | 289.13 g./mol | Molecular Formula: | C₁₂H₉BrN₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22552582 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting kinase enzymes. Its structure, featuring both indole and pyrimidine moieties, makes it a valuable scaffold for developing inhibitors that can modulate cellular signaling pathways. Researchers often explore its potential in designing drugs for cancer therapy, as kinase inhibitors are crucial in targeting tumor growth and proliferation. Additionally, it may be employed in the development of compounds for treating inflammatory and autoimmune diseases, where kinase activity plays a significant role. Its versatility and functional groups allow for further chemical modifications to optimize potency, selectivity, and pharmacokinetic properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,479.00 |
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4-(5-Bromo-1H-indol-3-yl)pyrimidin-2-amine
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting kinase enzymes. Its structure, featuring both indole and pyrimidine moieties, makes it a valuable scaffold for developing inhibitors that can modulate cellular signaling pathways. Researchers often explore its potential in designing drugs for cancer therapy, as kinase inhibitors are crucial in targeting tumor growth and proliferation. Additionally, it may be employed in the development of compounds for treating inflammatory and autoimmune diseases, where kinase activity plays a significant role. Its versatility and functional groups allow for further chemical modifications to optimize potency, selectivity, and pharmacokinetic properties.
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