(3-(pent-4-ynamido)phenyl)boronic acid
≥97%
- Product Code: 36634
CAS:
1392407-74-7
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| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in organic synthesis and medicinal chemistry due to its unique structure combining a boronic acid group and an alkyne functionality. The boronic acid group is widely employed in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds, which is crucial in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The alkyne group, on the other hand, allows for click chemistry reactions, such as the copper-catalyzed azide-alkyne cycloaddition (CuAAC), which is highly efficient and selective for bioconjugation and material science applications. Together, these features make it a versatile building block for the development of targeted drug delivery systems, bioactive molecules, and advanced materials. Additionally, its bifunctional nature can be exploited in the design of probes for bioimaging and sensing applications, where selective binding and labeling are required.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿6,345.00 |
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| 1.000 | 10-20 days | ฿15,669.00 |
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(3-(pent-4-ynamido)phenyl)boronic acid
This compound is primarily utilized in organic synthesis and medicinal chemistry due to its unique structure combining a boronic acid group and an alkyne functionality. The boronic acid group is widely employed in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds, which is crucial in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The alkyne group, on the other hand, allows for click chemistry reactions, such as the copper-catalyzed azide-alkyne cycloaddition (CuAAC), which is highly efficient and selective for bioconjugation and material science applications. Together, these features make it a versatile building block for the development of targeted drug delivery systems, bioactive molecules, and advanced materials. Additionally, its bifunctional nature can be exploited in the design of probes for bioimaging and sensing applications, where selective binding and labeling are required.
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