tert-Butyl 3-bromo-1H-pyrazole-1-carboxylate
98%
- Product Code: 45124
CAS:
1448855-35-3
| Molecular Weight: | 247.0891 g./mol | Molecular Formula: | C₈H₁₁BrN₂O₂ |
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| EC Number: | MDL Number: | MFCD25976492 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex compounds. It is particularly valuable in the pharmaceutical industry for constructing pyrazole derivatives, which are key structures in many biologically active molecules. The tert-butyl group provides steric protection, while the bromine atom offers a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings. Additionally, it is employed in the development of agrochemicals and materials science, where pyrazole-based compounds are utilized for their unique properties. Its stability and reactivity make it a useful building block in medicinal chemistry for drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $147.09 |
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tert-Butyl 3-bromo-1H-pyrazole-1-carboxylate
This chemical is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex compounds. It is particularly valuable in the pharmaceutical industry for constructing pyrazole derivatives, which are key structures in many biologically active molecules. The tert-butyl group provides steric protection, while the bromine atom offers a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings. Additionally, it is employed in the development of agrochemicals and materials science, where pyrazole-based compounds are utilized for their unique properties. Its stability and reactivity make it a useful building block in medicinal chemistry for drug discovery and development.
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