(R)-b-(Boc-amino)-2,5-difluorobenzenebutanoic acid
95%
- Product Code: 78469
CAS:
486459-98-7
| Molecular Weight: | 315.31 g./mol | Molecular Formula: | C₁₅H₁₉F₂NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09029663 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of peptide-based drugs. Its structure, featuring a Boc-protected amino group and difluorobenzene moiety, makes it a valuable intermediate in creating molecules with specific biological activities. It is often employed in medicinal chemistry research to design and produce inhibitors or modulators targeting enzymes or receptors. The difluorobenzene group enhances the compound's stability and binding affinity, while the Boc group allows for controlled deprotection during synthesis. This chemical is particularly relevant in the production of therapeutics for conditions such as cancer, inflammation, and metabolic disorders, where precise molecular interactions are critical. Its application extends to the development of advanced drug candidates with improved efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,293.00 |
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| 0.250 | 10-20 days | ฿7,920.00 |
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| 1.000 | 10-20 days | ฿19,809.00 |
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(R)-b-(Boc-amino)-2,5-difluorobenzenebutanoic acid
This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of peptide-based drugs. Its structure, featuring a Boc-protected amino group and difluorobenzene moiety, makes it a valuable intermediate in creating molecules with specific biological activities. It is often employed in medicinal chemistry research to design and produce inhibitors or modulators targeting enzymes or receptors. The difluorobenzene group enhances the compound's stability and binding affinity, while the Boc group allows for controlled deprotection during synthesis. This chemical is particularly relevant in the production of therapeutics for conditions such as cancer, inflammation, and metabolic disorders, where precise molecular interactions are critical. Its application extends to the development of advanced drug candidates with improved efficacy and selectivity.
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