tert-Butyl 3-(4-bromo-1H-pyrazol-1-yl)azetidine-1-carboxylate
98%
- Product Code: 149825
CAS:
877399-34-3
| Molecular Weight: | 302.17 g./mol | Molecular Formula: | C₁₁H₁₆BrN₃O₂ |
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| EC Number: | MDL Number: | MFCD17480368 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. The presence of the bromo-substituted pyrazole ring allows for further functionalization via cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, enabling the construction of complex molecular architectures. The tert-butoxycarbonyl (Boc) protecting group on the azetidine nitrogen ensures stability and selective deprotection under mild acidic conditions, making it valuable in multi-step synthetic routes. Commonly employed in medicinal chemistry for optimizing drug candidates targeting inflammatory, oncological, and central nervous system disorders.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $34.05 |
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| 0.250 | 10-20 days | $74.05 |
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| 1.000 | 10-20 days | $237.98 |
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| 5.000 | 10-20 days | $755.51 |
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tert-Butyl 3-(4-bromo-1H-pyrazol-1-yl)azetidine-1-carboxylate
Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. The presence of the bromo-substituted pyrazole ring allows for further functionalization via cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, enabling the construction of complex molecular architectures. The tert-butoxycarbonyl (Boc) protecting group on the azetidine nitrogen ensures stability and selective deprotection under mild acidic conditions, making it valuable in multi-step synthetic routes. Commonly employed in medicinal chemistry for optimizing drug candidates targeting inflammatory, oncological, and central nervous system disorders.
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