Benzyl (1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropyl)carbamate
95%
- Product Code: 152303
CAS:
1256359-24-6
| Molecular Weight: | 393.28 g./mol | Molecular Formula: | C₂₃H₂₈BNO₄ |
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| EC Number: | MDL Number: | MFCD16618967 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry |
Product Description:
Used as an intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in building functionalized cyclopropane derivatives. These structures are often found in bioactive compounds, including drug candidates with improved metabolic stability and target selectivity. Its protected amine group allows for further derivatization, supporting multi-step synthetic routes in medicinal chemistry.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £60.49 |
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| 0.250 | 10-20 days | £98.21 |
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| 1.000 | 10-20 days | £264.51 |
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| 5.000 | 10-20 days | £966.04 |
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Benzyl (1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropyl)carbamate
Used as an intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in building functionalized cyclopropane derivatives. These structures are often found in bioactive compounds, including drug candidates with improved metabolic stability and target selectivity. Its protected amine group allows for further derivatization, supporting multi-step synthetic routes in medicinal chemistry.
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