2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)acetic acid
≥95%
- Product Code: 194327
CAS:
1083326-41-3
| Molecular Weight: | 252.07 g./mol | Molecular Formula: | C₁₁H₁₇BN₂O₄ |
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| EC Number: | MDL Number: | MFCD16660234 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8℃ |
Product Description:
Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its pyrazole core linked to a boronate ester enables the formation of biaryl or heteroaryl structures, which are common motifs in pharmaceuticals and agrochemicals. The acetic acid group allows for further functionalization or conjugation, making it valuable in the development of complex molecules, including drug candidates and bioactive compounds. It is particularly useful in medicinal chemistry for constructing nitrogen-containing heterocyclic systems with high selectivity and efficiency.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 1g | 10-20 days | $80.63 |
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| 5g | 10-20 days | $389.89 |
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| 10g | 10-20 days | $776.06 |
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| 25g | 10-20 days | $1,933.53 |
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2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)acetic acid
Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its pyrazole core linked to a boronate ester enables the formation of biaryl or heteroaryl structures, which are common motifs in pharmaceuticals and agrochemicals. The acetic acid group allows for further functionalization or conjugation, making it valuable in the development of complex molecules, including drug candidates and bioactive compounds. It is particularly useful in medicinal chemistry for constructing nitrogen-containing heterocyclic systems with high selectivity and efficiency.
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