4-(1-Naphthyl)benzeneboronic acid
97%
- Product Code: 90324
Alias:
4-(1-Naphthyl)phenylboronic acid
CAS:
870774-25-7
Molecular Weight: | 248.09 g./mol | Molecular Formula: | C₁₆H₁₃BO₂ |
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EC Number: | MDL Number: | MFCD08669639 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and agrochemicals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to create complex organic molecules. This compound is also employed in the development of fluorescent probes and sensors due to its ability to interact with specific analytes. Additionally, it finds applications in materials science for the synthesis of advanced polymers and organic electronic materials. Its boronic acid group allows for versatile functionalization, making it useful in diverse research and industrial processes.
Product Specification:
Test | Specification |
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PURITYNEUTRALIZATION TITRATION | 97 112% |
APPEARANCE | WHITE TO OFF-WHITE POWDER OR CRYSTALS |
INFRARED SPECTROMETRY | Conforms to Structure |
PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿280.00 |
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1.000 | 10-20 days | ฿300.00 |
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5.000 | 10-20 days | ฿950.00 |
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25.000 | 10-20 days | ฿4,700.00 |
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100.000 | 10-20 days | ฿18,400.00 |
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4-(1-Naphthyl)benzeneboronic acid
Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and agrochemicals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to create complex organic molecules. This compound is also employed in the development of fluorescent probes and sensors due to its ability to interact with specific analytes. Additionally, it finds applications in materials science for the synthesis of advanced polymers and organic electronic materials. Its boronic acid group allows for versatile functionalization, making it useful in diverse research and industrial processes.
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