1-tert-Butyl 2-ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-1,2-dicarboxylate
97%
- Product Code: 39848
CAS:
1802005-04-4
| Molecular Weight: | 365.2290 g./mol | Molecular Formula: | C₁₈H₂₈BNO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30527899 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate, particularly in cross-coupling reactions. Its boronate ester functional group makes it valuable in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds. This reaction is essential in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, the tert-butyl and ethyl ester groups provide stability and reactivity, enabling selective transformations in multi-step synthetic pathways. Its application extends to the development of bioactive compounds and functional materials, where precise control over molecular structure is critical.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿3,555.00 |
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1-tert-Butyl 2-ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-1,2-dicarboxylate
This compound is primarily utilized in organic synthesis as a versatile intermediate, particularly in cross-coupling reactions. Its boronate ester functional group makes it valuable in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds. This reaction is essential in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, the tert-butyl and ethyl ester groups provide stability and reactivity, enabling selective transformations in multi-step synthetic pathways. Its application extends to the development of bioactive compounds and functional materials, where precise control over molecular structure is critical.
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