4-Chlorophenylboronic acid
97%
- Product Code: 90647
Alias:
4-Chlorophenylboronic acid; p-chlorophenylboronic acid
CAS:
1679-18-1
Molecular Weight: | 156.37 g./mol | Molecular Formula: | C₆H₆BClO₂ |
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EC Number: | 216-845-5 | MDL Number: | MFCD00039137 |
Melting Point: | 284-289 °C(lit.) | Boiling Point: | |
Density: | Storage Condition: | 2~8°C |
Product Description:
4-Chlorophenylboronic 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 biaryl compounds, which are common in drug development. Additionally, it serves as a building block in the synthesis of sensors and catalysts, contributing to advancements in chemical detection and industrial processes. Its stability and reactivity make it a preferred choice in various research and industrial applications.
Product Specification:
Test | Specification |
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Purity | 97-100 |
APPEARANCE | WHITE TO TAN CRYSTAL OR POWDER |
INFRARED SPECTRUM | Conforms to Structure |
HNMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿310.00 |
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5.000 | 10-20 days | ฿420.00 |
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25.000 | 10-20 days | ฿980.00 |
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100.000 | 10-20 days | ฿2,900.00 |
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500.000 | 10-20 days | ฿13,860.00 |
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4-Chlorophenylboronic acid
4-Chlorophenylboronic 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 biaryl compounds, which are common in drug development. Additionally, it serves as a building block in the synthesis of sensors and catalysts, contributing to advancements in chemical detection and industrial processes. Its stability and reactivity make it a preferred choice in various research and industrial applications.
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