2-Bromo-6-hydroxypyridine
98%
- Product Code: 144330
CAS:
27992-32-1
| Molecular Weight: | 174.00 g./mol | Molecular Formula: | C₅H₄BrNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00234043 | |
| Melting Point: | 121-125 °C | Boiling Point: | 336.6±42.0 °C(Predicted) |
| Density: | 1.776±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, seal, dry, light-proof |
Product Description:
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. It serves as a building block in the preparation of pyridine-based compounds with biological activity. Commonly employed in the manufacture of agrochemicals, including herbicides and fungicides, due to its ability to enhance molecular selectivity. Also utilized in research for the development of novel organic materials and catalysts. Its bromo and hydroxy functional groups allow for selective modifications, making it valuable in cross-coupling reactions and heterocyclic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White to Light Yellow to Purple Powder or Crystals |
| Purity | 97.5-100% |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 G | 10-20 days | ฿180.00 |
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| 5.000 G | 10-20 days | ฿750.00 |
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| 25.000 G | 10-20 days | ฿2,990.00 |
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| 100.000 G | 10-20 days | ฿7,210.00 |
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2-Bromo-6-hydroxypyridine
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. It serves as a building block in the preparation of pyridine-based compounds with biological activity. Commonly employed in the manufacture of agrochemicals, including herbicides and fungicides, due to its ability to enhance molecular selectivity. Also utilized in research for the development of novel organic materials and catalysts. Its bromo and hydroxy functional groups allow for selective modifications, making it valuable in cross-coupling reactions and heterocyclic chemistry.
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