2-Chloro-4-(4-methylpiperidin-1-yl)phenylboronic acid
95%
- Product Code: 91624
CAS:
2225169-54-8
| Molecular Weight: | 253.53288 g./mol | Molecular Formula: | C₁₂H₁₇BClNO₂ |
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| Density: | Storage Condition: | -20℃ |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables it to act as a key reagent in forming carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. It is especially useful in constructing complex aromatic and heteroaromatic structures, which are often found in active pharmaceutical ingredients. Additionally, its piperidine moiety can contribute to enhancing the solubility and bioavailability of the resulting compounds. This chemical is also employed in the synthesis of ligands for catalysis and in the preparation of intermediates for further chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | ฿11,592.00 |
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| 0.025 | 10-20 days | ฿23,292.00 |
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2-Chloro-4-(4-methylpiperidin-1-yl)phenylboronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables it to act as a key reagent in forming carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. It is especially useful in constructing complex aromatic and heteroaromatic structures, which are often found in active pharmaceutical ingredients. Additionally, its piperidine moiety can contribute to enhancing the solubility and bioavailability of the resulting compounds. This chemical is also employed in the synthesis of ligands for catalysis and in the preparation of intermediates for further chemical transformations.
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