2-(1-Piperidinyl)phenylboronic acid
98%
- Product Code: 89610
CAS:
1050505-85-5
| Molecular Weight: | 205.06 g./mol | Molecular Formula: | C₁₁H₁₆BNO₂ |
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| EC Number: | MDL Number: | MFCD03095111 | |
| Melting Point: | Boiling Point: | 391.6 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boron-containing reagent to form carbon-carbon bonds. Its phenylboronic acid group is essential for coupling with aryl halides, enabling the creation of complex organic molecules. Additionally, it finds application in the development of pharmaceuticals and agrochemicals, where it serves as a building block for bioactive compounds. Its piperidine moiety can also contribute to the modulation of drug-like properties, such as solubility and bioavailability. Furthermore, it is utilized in materials science for the synthesis of advanced polymers and functional materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft25,211.41 |
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| 0.250 | 10-20 days | Ft37,235.32 |
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2-(1-Piperidinyl)phenylboronic acid
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boron-containing reagent to form carbon-carbon bonds. Its phenylboronic acid group is essential for coupling with aryl halides, enabling the creation of complex organic molecules. Additionally, it finds application in the development of pharmaceuticals and agrochemicals, where it serves as a building block for bioactive compounds. Its piperidine moiety can also contribute to the modulation of drug-like properties, such as solubility and bioavailability. Furthermore, it is utilized in materials science for the synthesis of advanced polymers and functional materials.
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