4-Bromo-5-ethyl-1H-indazole
97%
- Product Code: 47472
CAS:
2109805-55-0
| Molecular Weight: | 225.09 g./mol | Molecular Formula: | C₉H₉BrN₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30729846 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
4-Bromo-5-ethyl-1H-indazole is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its structure is particularly valuable in the development of pharmaceutical agents, including potential inhibitors for enzymes and receptors involved in disease pathways. Researchers explore its use in creating molecules that target specific proteins, making it a crucial component in drug discovery efforts. Additionally, it serves as a building block in organic synthesis, enabling the construction of more complex heterocyclic compounds with potential therapeutic applications. Its bromo and ethyl substituents provide reactive sites for further chemical modifications, enhancing its versatility in designing novel drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿37,521.00 |
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4-Bromo-5-ethyl-1H-indazole
4-Bromo-5-ethyl-1H-indazole is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its structure is particularly valuable in the development of pharmaceutical agents, including potential inhibitors for enzymes and receptors involved in disease pathways. Researchers explore its use in creating molecules that target specific proteins, making it a crucial component in drug discovery efforts. Additionally, it serves as a building block in organic synthesis, enabling the construction of more complex heterocyclic compounds with potential therapeutic applications. Its bromo and ethyl substituents provide reactive sites for further chemical modifications, enhancing its versatility in designing novel drug candidates.
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