(S)-3-(3-Bromo-4-fluorophenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid
95%
- Product Code: 123715
CAS:
1329606-04-3
| Molecular Weight: | 362.19 g./mol | Molecular Formula: | C₁₄H₁₇BrFNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31704891 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. It serves as a key intermediate in the production of drugs targeting specific enzymes or receptors, often in the context of neurological or metabolic disorders. The presence of both bromo and fluoro substituents on the phenyl ring enhances its reactivity and selectivity in coupling reactions, making it valuable for constructing complex organic molecules. The tert-butoxycarbonyl (Boc) protecting group ensures stability during synthetic processes, allowing for precise modifications to the amino acid backbone. Its application is critical in medicinal chemistry for designing and optimizing drug candidates with improved efficacy and reduced side effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿24,669.00 |
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| 0.250 | 10-20 days | ฿36,963.00 |
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(S)-3-(3-Bromo-4-fluorophenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. It serves as a key intermediate in the production of drugs targeting specific enzymes or receptors, often in the context of neurological or metabolic disorders. The presence of both bromo and fluoro substituents on the phenyl ring enhances its reactivity and selectivity in coupling reactions, making it valuable for constructing complex organic molecules. The tert-butoxycarbonyl (Boc) protecting group ensures stability during synthetic processes, allowing for precise modifications to the amino acid backbone. Its application is critical in medicinal chemistry for designing and optimizing drug candidates with improved efficacy and reduced side effects.
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