2-Bromo-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazole
95%
- Product Code: 89809
CAS:
1402166-32-8
Molecular Weight: | 289.99 g./mol | Molecular Formula: | C₉H₁₃BBrNO₂S |
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EC Number: | MDL Number: | MFCD13181957 | |
Melting Point: | Boiling Point: | 341.0±15.0 °C(Predicted) | |
Density: | 1.44±0.1 g/cm3(Predicted) | Storage Condition: | -20°C, sealed, dry |
Product Description:
This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical research and drug development. It is often employed in the synthesis of thiazole-containing compounds, which are significant in medicinal chemistry due to their biological activity. Additionally, it serves as a building block in material science for creating advanced organic materials with specific electronic or optical properties. Its stability and reactivity make it a preferred choice for introducing thiazole moieties into target molecules.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.025 | 10-20 days | £23.82 |
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0.100 | 10-20 days | £47.83 |
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0.250 | 10-20 days | £107.48 |
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2-Bromo-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazole
This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical research and drug development. It is often employed in the synthesis of thiazole-containing compounds, which are significant in medicinal chemistry due to their biological activity. Additionally, it serves as a building block in material science for creating advanced organic materials with specific electronic or optical properties. Its stability and reactivity make it a preferred choice for introducing thiazole moieties into target molecules.
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