(2-(Benzyloxy)naphthalen-1-yl)boronic acid
98%
- Product Code: 85777
CAS:
219834-96-5
| Molecular Weight: | 278.11 g./mol | Molecular Formula: | C₁₇H₁₅BO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16295233 | |
| Melting Point: | Boiling Point: | 517.6±52.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in creating complex organic molecules. Additionally, it finds applications in the development of fluorescent probes and sensors due to its naphthalene structure, which exhibits strong photophysical properties. Its versatility in coupling reactions also makes it useful in polymer chemistry for designing specialized polymers with tailored properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,112.00 |
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| 1.000 | 10-20 days | ฿10,224.00 |
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(2-(Benzyloxy)naphthalen-1-yl)boronic acid
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in creating complex organic molecules. Additionally, it finds applications in the development of fluorescent probes and sensors due to its naphthalene structure, which exhibits strong photophysical properties. Its versatility in coupling reactions also makes it useful in polymer chemistry for designing specialized polymers with tailored properties.
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