3-Iodo-1H-indazol-4-amine
97%
- Product Code: 45568
CAS:
885521-28-8
| Molecular Weight: | 259.0500 g./mol | Molecular Formula: | C₇H₆IN₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07781576 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
3-Iodo-1H-indazol-4-amine is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active compounds. Its structure is particularly valuable in the design of inhibitors targeting specific enzymes or receptors, making it a crucial component in drug discovery efforts. The compound is often employed in the preparation of potential therapeutic agents for treating diseases such as cancer, inflammation, and infectious diseases. Additionally, it serves as a building block in organic synthesis, enabling the creation of complex molecules with potential applications in medicinal chemistry. Its iodine moiety also makes it a useful substrate for further functionalization through cross-coupling reactions, expanding its utility in the development of novel compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,673.00 |
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3-Iodo-1H-indazol-4-amine
3-Iodo-1H-indazol-4-amine is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active compounds. Its structure is particularly valuable in the design of inhibitors targeting specific enzymes or receptors, making it a crucial component in drug discovery efforts. The compound is often employed in the preparation of potential therapeutic agents for treating diseases such as cancer, inflammation, and infectious diseases. Additionally, it serves as a building block in organic synthesis, enabling the creation of complex molecules with potential applications in medicinal chemistry. Its iodine moiety also makes it a useful substrate for further functionalization through cross-coupling reactions, expanding its utility in the development of novel compounds.
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