Methyl 5-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate
97%
- Product Code: 48742
CAS:
1227664-24-5
| Molecular Weight: | 302.5820 g./mol | Molecular Formula: | C₁₂H₁₆BClO₄S |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate. Its boronate ester functionality makes it valuable in Suzuki-Miyaura coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. It is often employed in the development of pharmaceuticals and agrochemicals, where precise molecular construction is critical. Additionally, its thiophene moiety is useful in materials science, particularly in the design of organic semiconductors and conductive polymers. The compound’s stability and reactivity make it a versatile tool in advanced chemical research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,223.00 |
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Methyl 5-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate. Its boronate ester functionality makes it valuable in Suzuki-Miyaura coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. It is often employed in the development of pharmaceuticals and agrochemicals, where precise molecular construction is critical. Additionally, its thiophene moiety is useful in materials science, particularly in the design of organic semiconductors and conductive polymers. The compound’s stability and reactivity make it a versatile tool in advanced chemical research and industrial applications.
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