1-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-thiazol-2-yl]ethanone
95%
- Product Code: 89492
CAS:
1452577-24-0
| Molecular Weight: | 253.13 g./mol | Molecular Formula: | C₁₁H₁₆BNO₃S |
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| EC Number: | MDL Number: | MFCD22056534 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it serves as a key intermediate for constructing complex molecules. Its boronate ester group makes it highly effective for forming carbon-carbon bonds, enabling the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is utilized in the development of heterocyclic compounds, especially thiazole derivatives, which are important in medicinal chemistry for their biological activities. Its stability and reactivity also make it a valuable reagent in research and industrial applications for creating diverse chemical structures.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.005 | 10-20 days | $421.83 |
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| 0.025 | 10-20 days | $929.89 |
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1-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-thiazol-2-yl]ethanone
This chemical is widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it serves as a key intermediate for constructing complex molecules. Its boronate ester group makes it highly effective for forming carbon-carbon bonds, enabling the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is utilized in the development of heterocyclic compounds, especially thiazole derivatives, which are important in medicinal chemistry for their biological activities. Its stability and reactivity also make it a valuable reagent in research and industrial applications for creating diverse chemical structures.
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