6(S)-5-BOC-1,1-DIFLUORO-5-AZASPIRO[2.4]HEPTANE-6-CARBOXYLIC ACID
95%
- Product Code: 66082
CAS:
1357482-03-1
| Molecular Weight: | 277 g./mol | Molecular Formula: | C₁₂H₁₇F₂NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD21362512 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed and dry |
Product Description:
This compound is primarily utilized in the pharmaceutical and medicinal chemistry fields as a key intermediate in the synthesis of biologically active molecules. Its unique spirocyclic structure and functional groups make it valuable for developing novel drug candidates, particularly in the design of enzyme inhibitors and receptor modulators. The BOC-protected amine and carboxylic acid groups allow for further chemical modifications, enabling the creation of complex molecules with potential therapeutic applications. It is often employed in the research and development of drugs targeting neurological disorders, cancer, and infectious diseases, where its structural features contribute to enhanced stability and bioavailability. Additionally, its difluorinated moiety can improve metabolic stability and binding affinity in drug molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €1,164.24 |
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| 0.500 | 10-20 days | €3,677.39 |
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6(S)-5-BOC-1,1-DIFLUORO-5-AZASPIRO[2.4]HEPTANE-6-CARBOXYLIC ACID
This compound is primarily utilized in the pharmaceutical and medicinal chemistry fields as a key intermediate in the synthesis of biologically active molecules. Its unique spirocyclic structure and functional groups make it valuable for developing novel drug candidates, particularly in the design of enzyme inhibitors and receptor modulators. The BOC-protected amine and carboxylic acid groups allow for further chemical modifications, enabling the creation of complex molecules with potential therapeutic applications. It is often employed in the research and development of drugs targeting neurological disorders, cancer, and infectious diseases, where its structural features contribute to enhanced stability and bioavailability. Additionally, its difluorinated moiety can improve metabolic stability and binding affinity in drug molecules.
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