1-(2-Cyanophenyl)piperidine-4-carboxylic Acid
≥97%
- Product Code: 57186
CAS:
937601-79-1
| Molecular Weight: | 230.26 g./mol | Molecular Formula: | C₁₃H₁₄N₂O₂ |
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| EC Number: | MDL Number: | MFCD08689748 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring both a cyano group and a carboxylic acid moiety, makes it a versatile building block for designing and developing new drugs. It is often employed in the creation of compounds targeting neurological disorders, particularly those involving modulation of neurotransmitter systems. Additionally, it serves as a precursor in the development of potential analgesics and anti-inflammatory agents, owing to its ability to interact with specific biological targets. Its applications also extend to research in organic synthesis, where it is used to explore novel chemical reactions and pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿5,560.00 |
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| 5.000 | 10-20 days | ฿17,430.00 |
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1-(2-Cyanophenyl)piperidine-4-carboxylic Acid
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring both a cyano group and a carboxylic acid moiety, makes it a versatile building block for designing and developing new drugs. It is often employed in the creation of compounds targeting neurological disorders, particularly those involving modulation of neurotransmitter systems. Additionally, it serves as a precursor in the development of potential analgesics and anti-inflammatory agents, owing to its ability to interact with specific biological targets. Its applications also extend to research in organic synthesis, where it is used to explore novel chemical reactions and pathways.
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