Methyl 5-bromo-2-chloropyridine-3-carboxylate
98%
- Product Code: 48925
CAS:
78686-79-0
| Molecular Weight: | 250.48 g./mol | Molecular Formula: | C₇H₅BrClNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 50-52°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring both bromo and chloro substituents, makes it a versatile building block for creating complex heterocyclic compounds. It is often employed in the preparation of potential drug candidates, particularly in the development of kinase inhibitors, which are crucial in treating cancers and inflammatory diseases. Additionally, it serves as a precursor in organic synthesis for constructing pyridine-based scaffolds, which are widely explored in medicinal chemistry for their therapeutic potential. Its role in facilitating the introduction of functional groups further enhances its importance in designing novel chemical entities.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White - Pale reddish yellow Crystal - Powder |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
| NOTE: | This product is low melting point solid,may change state in different environments (solid, liquid or semi-solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿520.00 |
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| 10.000 | 10-20 days | ฿1,020.00 |
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| 25.000 | 10-20 days | ฿2,440.00 |
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Methyl 5-bromo-2-chloropyridine-3-carboxylate
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring both bromo and chloro substituents, makes it a versatile building block for creating complex heterocyclic compounds. It is often employed in the preparation of potential drug candidates, particularly in the development of kinase inhibitors, which are crucial in treating cancers and inflammatory diseases. Additionally, it serves as a precursor in organic synthesis for constructing pyridine-based scaffolds, which are widely explored in medicinal chemistry for their therapeutic potential. Its role in facilitating the introduction of functional groups further enhances its importance in designing novel chemical entities.
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