(2S,4R)-4-(3-Fluorobenzyl)pyrrolidine-2-carboxylic acid
98%
- Product Code: 123618
CAS:
1262526-44-2
| Molecular Weight: | 223.24 g./mol | Molecular Formula: | C₁₂H₁₄FNO₂ |
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| EC Number: | MDL Number: | MFCD07363501 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry, protected from light |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate or building block in the synthesis of pharmaceutical agents, particularly those targeting neurological and psychiatric disorders. Its structure is often incorporated into molecules designed to interact with specific receptors or enzymes in the central nervous system, potentially aiding in the treatment of conditions such as depression, anxiety, or neurodegenerative diseases. Additionally, its fluorinated benzyl group enhances its binding affinity and metabolic stability, making it a valuable component in the design of bioactive compounds. Researchers also explore its use in creating peptide mimetics or as a chiral scaffold for asymmetric synthesis in organic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $388.71 |
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| 0.250 | 10-20 days | $728.83 |
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| 1.000 | 10-20 days | $1,822.08 |
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(2S,4R)-4-(3-Fluorobenzyl)pyrrolidine-2-carboxylic acid
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate or building block in the synthesis of pharmaceutical agents, particularly those targeting neurological and psychiatric disorders. Its structure is often incorporated into molecules designed to interact with specific receptors or enzymes in the central nervous system, potentially aiding in the treatment of conditions such as depression, anxiety, or neurodegenerative diseases. Additionally, its fluorinated benzyl group enhances its binding affinity and metabolic stability, making it a valuable component in the design of bioactive compounds. Researchers also explore its use in creating peptide mimetics or as a chiral scaffold for asymmetric synthesis in organic chemistry.
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