(3-(Adamantan-1-yl)-4-methoxyphenyl)boronic acid
96%
- Product Code: 117376
CAS:
459423-32-6
| Molecular Weight: | 286.17 g./mol | Molecular Formula: | C₁₇H₂₃BO₃ |
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| EC Number: | MDL Number: | MFCD08056355 | |
| Melting Point: | Boiling Point: | 475°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
(3-(Adamantan-1-yl)-4-methoxyphenyl)boronic acid is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry for the construction of biaryl compounds, which are essential in the development of various drugs and bioactive molecules. The adamantyl group in the compound enhances its stability and solubility, making it a valuable reagent in complex synthetic pathways. Additionally, it is used in the preparation of advanced materials, such as organic semiconductors and polymers, due to its ability to facilitate the formation of carbon-carbon bonds. Its unique structure also makes it a potential candidate for research in medicinal chemistry, particularly in the design of enzyme inhibitors and receptor ligands.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,431.00 |
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| 0.250 | 10-20 days | ฿2,151.00 |
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| 1.000 | 10-20 days | ฿5,364.00 |
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| 5.000 | 10-20 days | ฿17,145.00 |
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(3-(Adamantan-1-yl)-4-methoxyphenyl)boronic acid
(3-(Adamantan-1-yl)-4-methoxyphenyl)boronic acid is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry for the construction of biaryl compounds, which are essential in the development of various drugs and bioactive molecules. The adamantyl group in the compound enhances its stability and solubility, making it a valuable reagent in complex synthetic pathways. Additionally, it is used in the preparation of advanced materials, such as organic semiconductors and polymers, due to its ability to facilitate the formation of carbon-carbon bonds. Its unique structure also makes it a potential candidate for research in medicinal chemistry, particularly in the design of enzyme inhibitors and receptor ligands.
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