4-Chloro-1-(4-methoxybenzyl)-1H-imidazo[4,5-c]pyridine-2(3H)-thione
95%
- Product Code: 47044
CAS:
1012059-49-2
| Molecular Weight: | 305.78 g./mol | Molecular Formula: | C₁₄H₁₂ClN₃OS |
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| 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 is particularly valuable in the development of potential therapeutic agents, especially those targeting enzymes or receptors involved in inflammatory and immune responses. Researchers have explored its derivatives for their potential as inhibitors of specific kinases, which play a critical role in cell signaling pathways associated with diseases like cancer and autoimmune disorders. Additionally, its unique imidazo[4,5-c]pyridine core makes it a promising scaffold for designing compounds with antiviral or antimicrobial properties. The presence of the chloro and methoxybenzyl groups allows for further chemical modifications, enabling the creation of diverse analogs with optimized pharmacological profiles.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,991.00 |
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4-Chloro-1-(4-methoxybenzyl)-1H-imidazo[4,5-c]pyridine-2(3H)-thione
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 is particularly valuable in the development of potential therapeutic agents, especially those targeting enzymes or receptors involved in inflammatory and immune responses. Researchers have explored its derivatives for their potential as inhibitors of specific kinases, which play a critical role in cell signaling pathways associated with diseases like cancer and autoimmune disorders. Additionally, its unique imidazo[4,5-c]pyridine core makes it a promising scaffold for designing compounds with antiviral or antimicrobial properties. The presence of the chloro and methoxybenzyl groups allows for further chemical modifications, enabling the creation of diverse analogs with optimized pharmacological profiles.
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