2-((5-Bromo-4-methylpyridin-2-yl)amino)ethanol
95%
- Product Code: 41156
CAS:
1219982-86-1
| Molecular Weight: | 231.1000 g./mol | Molecular Formula: | C₈H₁₁BrN₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13562416 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of pharmaceutical research and development, where it serves as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring a bromo and methyl-substituted pyridine ring, makes it a valuable building block for creating molecules with potential therapeutic properties. It is often employed in the design of drugs targeting specific enzymes or receptors, particularly in the development of kinase inhibitors, which are crucial in treating diseases like cancer and inflammatory disorders. Additionally, its ethanolamine moiety allows for further functionalization, enabling the creation of derivatives with enhanced pharmacological profiles. Researchers also explore its use in the development of diagnostic agents and probes for studying biological pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,719.00 |
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2-((5-Bromo-4-methylpyridin-2-yl)amino)ethanol
This chemical is primarily utilized in the field of pharmaceutical research and development, where it serves as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring a bromo and methyl-substituted pyridine ring, makes it a valuable building block for creating molecules with potential therapeutic properties. It is often employed in the design of drugs targeting specific enzymes or receptors, particularly in the development of kinase inhibitors, which are crucial in treating diseases like cancer and inflammatory disorders. Additionally, its ethanolamine moiety allows for further functionalization, enabling the creation of derivatives with enhanced pharmacological profiles. Researchers also explore its use in the development of diagnostic agents and probes for studying biological pathways.
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