(4-((naphthalen-1-ylamino)methyl)phenyl)boronic acid
95%
- Product Code: 218341
CAS:
1029439-61-9
| Molecular Weight: | 277.12544 g./mol | Molecular Formula: | C₁₇H₁₆BNO₂ |
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| EC Number: | MDL Number: | MFCD31916483 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature |
Product Description:
Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical research. Its boronic acid group facilitates coupling with aryl halides, making it valuable in the development of complex aromatic compounds. The presence of a naphthylamino group enhances conjugation and stability in resulting products, useful in materials science for designing organic semiconductors or fluorescent probes. Also explored in medicinal chemistry for targeted synthesis of bioactive molecules due to its structural rigidity and binding potential.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿15,680.00 |
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| 1g | 10-20 days | ฿32,000.00 |
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| 5g | 10-20 days | ฿104,000.00 |
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(4-((naphthalen-1-ylamino)methyl)phenyl)boronic acid
Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical research. Its boronic acid group facilitates coupling with aryl halides, making it valuable in the development of complex aromatic compounds. The presence of a naphthylamino group enhances conjugation and stability in resulting products, useful in materials science for designing organic semiconductors or fluorescent probes. Also explored in medicinal chemistry for targeted synthesis of bioactive molecules due to its structural rigidity and binding potential.
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