3-Iodo-4-(piperidin-1-ylmethyl)benzoic acid
95%
- Product Code: 45579
CAS:
1131614-61-3
| Molecular Weight: | 345.1761 g./mol | Molecular Formula: | C₁₃H₁₆INO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11110810 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both an iodo group and a piperidinylmethyl moiety, makes it a valuable building block for developing potential drug candidates, particularly in the design of small-molecule inhibitors targeting specific enzymes or receptors. It is often employed in the preparation of compounds with potential therapeutic applications, such as anti-inflammatory, anticancer, or antimicrobial agents. Additionally, its iodine atom allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery and optimization.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £69.21 |
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3-Iodo-4-(piperidin-1-ylmethyl)benzoic acid
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both an iodo group and a piperidinylmethyl moiety, makes it a valuable building block for developing potential drug candidates, particularly in the design of small-molecule inhibitors targeting specific enzymes or receptors. It is often employed in the preparation of compounds with potential therapeutic applications, such as anti-inflammatory, anticancer, or antimicrobial agents. Additionally, its iodine atom allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery and optimization.
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