(3-Phenylnaphthalen-1-yl)boronic acid
95%
- Product Code: 131931
CAS:
1922905-62-1
| Molecular Weight: | 248.08 g./mol | Molecular Formula: | C₁₆H₁₃BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD29472450 | |
| Melting Point: | Boiling Point: | 486.0±48.0 °C(Predicted) | |
| Density: | 1.23±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature, seal, inert gas |
Product Description:
Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. It serves as a key building block in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables selective carbon-carbon bond formation under mild conditions, making it valuable in medicinal chemistry for constructing complex aromatic frameworks. Also applied in the preparation of fluorescent dyes and organic semiconductors due to the extended π-conjugation from the naphthalene and phenyl groups.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,550.00 |
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| 1.000 | 10-20 days | ฿6,890.00 |
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| 5.000 | 10-20 days | ฿24,070.00 |
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(3-Phenylnaphthalen-1-yl)boronic acid
Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. It serves as a key building block in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables selective carbon-carbon bond formation under mild conditions, making it valuable in medicinal chemistry for constructing complex aromatic frameworks. Also applied in the preparation of fluorescent dyes and organic semiconductors due to the extended π-conjugation from the naphthalene and phenyl groups.
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