Methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-2-carboxylate
98%
- Product Code: 211677
CAS:
1198605-53-6
| Molecular Weight: | 251.09 g./mol | Molecular Formula: | C₁₂H₁₈BNO₄ |
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| EC Number: | MDL Number: | MFCD16995409 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing complex molecules in pharmaceutical and agrochemical research. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable for creating biaryl and heteroaryl systems. Its pyrrole core is common in bioactive compounds, so this reagent is often employed in the development of drug candidates, especially those targeting central nervous system disorders and inflammation. Additionally, it is used in materials science for synthesizing conjugated polymers and organic electronic materials due to the electron-rich nature of the pyrrole ring. The ester functionality allows for further derivatization, enhancing its utility in multi-step syntheses.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿2,630.00 |
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| 1g | 10-20 days | ฿11,500.00 |
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| 5g | 10-20 days | ฿40,250.00 |
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| 250mg | 10-20 days | ฿4,270.00 |
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Methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-2-carboxylate
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing complex molecules in pharmaceutical and agrochemical research. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable for creating biaryl and heteroaryl systems. Its pyrrole core is common in bioactive compounds, so this reagent is often employed in the development of drug candidates, especially those targeting central nervous system disorders and inflammation. Additionally, it is used in materials science for synthesizing conjugated polymers and organic electronic materials due to the electron-rich nature of the pyrrole ring. The ester functionality allows for further derivatization, enhancing its utility in multi-step syntheses.
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