(4-(2-((tert-Butoxycarbonyl)(cyclopropyl)amino)ethoxy)phenyl)boronic acid
98%
- Product Code: 89226
CAS:
1704080-18-1
Molecular Weight: | 321.18 g./mol | Molecular Formula: | C₁₆H₂₄BNO₅ |
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EC Number: | MDL Number: | MFCD28400396 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic acid derivative, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its structure, featuring a tert-butoxycarbonyl-protected amine and a cyclopropyl group, makes it valuable in medicinal chemistry for the development of pharmaceutical intermediates. Additionally, it is employed in the preparation of biologically active compounds, including potential drug candidates targeting various diseases. The compound’s stability and reactivity make it a useful reagent in the design and synthesis of novel chemical entities for research and industrial applications.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.500 | 10-20 days | £651.60 |
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(4-(2-((tert-Butoxycarbonyl)(cyclopropyl)amino)ethoxy)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic acid derivative, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its structure, featuring a tert-butoxycarbonyl-protected amine and a cyclopropyl group, makes it valuable in medicinal chemistry for the development of pharmaceutical intermediates. Additionally, it is employed in the preparation of biologically active compounds, including potential drug candidates targeting various diseases. The compound’s stability and reactivity make it a useful reagent in the design and synthesis of novel chemical entities for research and industrial applications.
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