(S)-2-amino-2-(2-bromo-4-fluorophenyl)acetic acid hcl
95%
- Product Code: 81928
CAS:
1391551-89-5
| Molecular Weight: | 284.51 g./mol | Molecular Formula: | C₈H₈BrClFNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12759257 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, inert gas |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of drugs targeting specific biological pathways, often in the development of enzyme inhibitors or receptor modulators. Its structural features, including the bromo and fluoro substituents, make it valuable for creating molecules with enhanced binding affinity and selectivity. Additionally, it is explored in medicinal chemistry for the design of compounds with potential therapeutic applications in treating neurological disorders or inflammatory conditions. Its role in chiral synthesis is also notable, as it contributes to the production of enantiomerically pure drugs, which are critical for optimizing efficacy and reducing side effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $786.09 |
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| 0.250 | 10-20 days | $1,177.55 |
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(S)-2-amino-2-(2-bromo-4-fluorophenyl)acetic acid hcl
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of drugs targeting specific biological pathways, often in the development of enzyme inhibitors or receptor modulators. Its structural features, including the bromo and fluoro substituents, make it valuable for creating molecules with enhanced binding affinity and selectivity. Additionally, it is explored in medicinal chemistry for the design of compounds with potential therapeutic applications in treating neurological disorders or inflammatory conditions. Its role in chiral synthesis is also notable, as it contributes to the production of enantiomerically pure drugs, which are critical for optimizing efficacy and reducing side effects.
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