2-Biphenylboronic acid
97%
- Product Code: 89877
Alias:
2-Biphenylboronic acid
CAS:
4688-76-0
Molecular Weight: | 198.03 g./mol | Molecular Formula: | C₆H₅C₆H₄BOH₂ |
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EC Number: | MDL Number: | MFCD00136929 | |
Melting Point: | 167-172 °C(lit.) | Boiling Point: | 404ºC at 760 mmHg |
Density: | 1.18 g/cm3 | Storage Condition: | room temperature |
Product Description:
2-Biphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the creation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its role as a boronic acid derivative makes it a valuable reagent for constructing biphenyl structures, which are common in many active pharmaceutical ingredients. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with various organic and inorganic compounds. Its stability and reactivity under mild conditions further enhance its utility in research and industrial applications.
Product Specification:
Test | Specification |
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Purity | 97-100 |
SUITABILITY TEST | PASSES |
APPEARANCE | WHITE TO OFF-WHITE POWDER OR CRYSTALS |
INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿300.00 |
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5.000 | 10-20 days | ฿1,300.00 |
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25.000 | 10-20 days | ฿4,080.00 |
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100.000 | 10-20 days | ฿14,880.00 |
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2-Biphenylboronic acid
2-Biphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the creation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its role as a boronic acid derivative makes it a valuable reagent for constructing biphenyl structures, which are common in many active pharmaceutical ingredients. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with various organic and inorganic compounds. Its stability and reactivity under mild conditions further enhance its utility in research and industrial applications.
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