(S)-tert-Butyl 6-(5-(7-bromo-9,9-difluoro-9H-fluoren-2-yl)-1H-imidazol-2-yl)-5-azaspiro[2.4]heptane-5-carboxylate
97%
- Product Code: 235673
CAS:
1441670-89-8
| Molecular Weight: | 542.42 g./mol | Molecular Formula: | C₂₇H₂₆BrF₂N₃O₂ |
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| EC Number: | MDL Number: | MFCD28386931 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry seal |
Product Description:
Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure supports the development of selective drug candidates due to the spirocyclic core and imidazole functionality, which enhance binding affinity and metabolic stability. Commonly employed in medicinal chemistry for constructing complex molecules with potential anticancer and anti-inflammatory activity. The bromo and difluoro substituents allow further functionalization via cross-coupling reactions, making it valuable in SAR studies and lead optimization.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $43.00 |
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| 5.000 | 10-20 days | $415.51 |
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| 25.000 | 10-20 days | $2,075.99 |
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| 1.000 | 10-20 days | $106.73 |
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(S)-tert-Butyl 6-(5-(7-bromo-9,9-difluoro-9H-fluoren-2-yl)-1H-imidazol-2-yl)-5-azaspiro[2.4]heptane-5-carboxylate
Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure supports the development of selective drug candidates due to the spirocyclic core and imidazole functionality, which enhance binding affinity and metabolic stability. Commonly employed in medicinal chemistry for constructing complex molecules with potential anticancer and anti-inflammatory activity. The bromo and difluoro substituents allow further functionalization via cross-coupling reactions, making it valuable in SAR studies and lead optimization.
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