3-(Cyclopentylaminocarbonyl)phenylboronic acid
98%
- Product Code: 90042
CAS:
850567-24-7
| Molecular Weight: | 233.07 g./mol | Molecular Formula: | C₁₂H₁₆BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04115695 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent to facilitate the formation of carbon-carbon bonds. Its structure, featuring a cyclopentylaminocarbonyl group, enhances its stability and reactivity, making it suitable for constructing complex organic molecules, such as pharmaceuticals and agrochemicals. Additionally, it can be employed in the development of sensors or probes for detecting specific analytes, leveraging its boronic acid moiety’s ability to bind with diols or other target molecules. Its applications also extend to materials science, where it may be used in the modification of polymers or surfaces to impart specific functional properties.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to yellowish brown solid |
| PURITY | 97.5 100% |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | $92.02 |
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| 1.000 | 10-20 days | $276.07 |
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| 5.000 | 10-20 days | $1,164.05 |
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3-(Cyclopentylaminocarbonyl)phenylboronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent to facilitate the formation of carbon-carbon bonds. Its structure, featuring a cyclopentylaminocarbonyl group, enhances its stability and reactivity, making it suitable for constructing complex organic molecules, such as pharmaceuticals and agrochemicals. Additionally, it can be employed in the development of sensors or probes for detecting specific analytes, leveraging its boronic acid moiety’s ability to bind with diols or other target molecules. Its applications also extend to materials science, where it may be used in the modification of polymers or surfaces to impart specific functional properties.
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