(R)-3-tert-Butoxycarbonylamino-3-(3-fluorophenyl)propionic acid
98%
- Product Code: 104644
CAS:
500789-04-8
Molecular Weight: | 283.30 g./mol | Molecular Formula: | C₁₄H₁₈FNO₄ |
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EC Number: | MDL Number: | MFCD03427956 | |
Melting Point: | Boiling Point: | 422.1°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a fluorophenyl group and a tert-butoxycarbonyl (Boc) protected amine, makes it valuable in the development of peptide-based drugs and small molecule inhibitors. The fluorine atom enhances the metabolic stability and binding affinity of the final compounds, while the Boc group provides protection during synthetic processes, ensuring selective reactions. It is particularly relevant in the production of drugs targeting neurological disorders, cancer, and inflammation, where precise molecular interactions are critical. The compound’s chiral center also allows for the creation of enantiomerically pure substances, which is essential for optimizing therapeutic efficacy and reducing side effects.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿2,259.00 |
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1.000 | 10-20 days | ฿4,707.00 |
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5.000 | 10-20 days | ฿23,490.00 |
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(R)-3-tert-Butoxycarbonylamino-3-(3-fluorophenyl)propionic acid
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a fluorophenyl group and a tert-butoxycarbonyl (Boc) protected amine, makes it valuable in the development of peptide-based drugs and small molecule inhibitors. The fluorine atom enhances the metabolic stability and binding affinity of the final compounds, while the Boc group provides protection during synthetic processes, ensuring selective reactions. It is particularly relevant in the production of drugs targeting neurological disorders, cancer, and inflammation, where precise molecular interactions are critical. The compound’s chiral center also allows for the creation of enantiomerically pure substances, which is essential for optimizing therapeutic efficacy and reducing side effects.
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