tert-Butyl 3-bromo-1H-indazole-1-carboxylate
97%
- Product Code: 45129
CAS:
1257296-40-4
| Molecular Weight: | 297.1600 g./mol | Molecular Formula: | C₁₂H₁₃BrN₂O₂ |
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| EC Number: | MDL Number: | MFCD22380231 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of various biologically active molecules, particularly in pharmaceutical research. It serves as a key building block in the development of indazole-based compounds, which are known for their potential therapeutic properties, including anti-inflammatory, anticancer, and antimicrobial activities. The tert-butyl group provides steric protection, enhancing the stability of the molecule during chemical transformations, while the bromo substituent allows for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings. Its application is particularly significant in the design and synthesis of drug candidates targeting specific enzymes or receptors in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £77.35 |
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tert-Butyl 3-bromo-1H-indazole-1-carboxylate
This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of various biologically active molecules, particularly in pharmaceutical research. It serves as a key building block in the development of indazole-based compounds, which are known for their potential therapeutic properties, including anti-inflammatory, anticancer, and antimicrobial activities. The tert-butyl group provides steric protection, enhancing the stability of the molecule during chemical transformations, while the bromo substituent allows for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings. Its application is particularly significant in the design and synthesis of drug candidates targeting specific enzymes or receptors in medicinal chemistry.
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