(4-(1-((tert-Butoxycarbonyl)amino)cyclopropyl)phenyl)boronic acid
98%
- Product Code: 89214
CAS:
1217500-58-7
| Molecular Weight: | 277.12 g./mol | Molecular Formula: | C₁₄H₂₀BNO₄ |
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| EC Number: | MDL Number: | MFCD12546458 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl groups. This makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The tert-butoxycarbonyl (Boc) protecting group enhances its stability during reactions, allowing for selective deprotection in multi-step synthesis processes. Its cyclopropyl group also contributes to unique steric and electronic properties, which can be exploited in the design of bioactive compounds or materials with specific functionalities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £44.58 |
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| 0.250 | 10-20 days | £75.52 |
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(4-(1-((tert-Butoxycarbonyl)amino)cyclopropyl)phenyl)boronic acid
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl groups. This makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The tert-butoxycarbonyl (Boc) protecting group enhances its stability during reactions, allowing for selective deprotection in multi-step synthesis processes. Its cyclopropyl group also contributes to unique steric and electronic properties, which can be exploited in the design of bioactive compounds or materials with specific functionalities.
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