1-(Pyridin-4-yl)-1H-imidazole-5-carboxylic acid
97%
- Product Code: 39595
CAS:
1439900-49-8
| Molecular Weight: | 189.1708 g./mol | Molecular Formula: | C₉H₇N₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26096963 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development due to its structural framework, which is often associated with biological activity. It serves as a key intermediate or building block in the synthesis of various pharmaceutical agents, particularly those targeting enzymes or receptors. Its pyridine and imidazole moieties make it a versatile scaffold for designing molecules with potential therapeutic applications, such as anti-inflammatory, antimicrobial, or anticancer agents. Additionally, it is explored in the development of small-molecule inhibitors for specific biological pathways, contributing to advancements in targeted therapy research. Its carboxylic acid group also allows for further functionalization, enabling the creation of derivatives with optimized pharmacokinetic properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,101.00 |
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1-(Pyridin-4-yl)-1H-imidazole-5-carboxylic acid
This compound is primarily utilized in the field of medicinal chemistry and drug development due to its structural framework, which is often associated with biological activity. It serves as a key intermediate or building block in the synthesis of various pharmaceutical agents, particularly those targeting enzymes or receptors. Its pyridine and imidazole moieties make it a versatile scaffold for designing molecules with potential therapeutic applications, such as anti-inflammatory, antimicrobial, or anticancer agents. Additionally, it is explored in the development of small-molecule inhibitors for specific biological pathways, contributing to advancements in targeted therapy research. Its carboxylic acid group also allows for further functionalization, enabling the creation of derivatives with optimized pharmacokinetic properties.
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