(4'-Acetyl-[1,1'-biphenyl]-4-yl)boronic acid

98%

Reagent Code: #123631
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CAS Number 1029438-14-9

science Other reagents with same CAS 1029438-14-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.07 g/mol
Formula C₁₄H₁₃BO₃
badge Registry Numbers
MDL Number MFCD16295057
thermostat Physical Properties
Boiling Point 441.5±47.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.22±0.1 g/cm3(Predicted)
Storage Room temperature, dark, inert gas

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a key intermediate for constructing complex biphenyl structures, which are often found in pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds. Additionally, it is employed in the development of organic electronic materials and liquid crystals due to its ability to form stable and functionalized biphenyl derivatives. Its applications also extend to medicinal chemistry, where it is used in the synthesis of bioactive molecules and drug candidates.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,339.00
inventory 1g
10-20 days ฿9,000.00
inventory 100mg
10-20 days ฿1,971.00

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(4'-Acetyl-[1,1'-biphenyl]-4-yl)boronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a key intermediate for constructing complex biphenyl structures, which are often found in pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds. Additionally, it is employed in the development of organic electronic materials and liquid crystals due to its abil

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a key intermediate for constructing complex biphenyl structures, which are often found in pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds. Additionally, it is employed in the development of organic electronic materials and liquid crystals due to its ability to form stable and functionalized biphenyl derivatives. Its applications also extend to medicinal chemistry, where it is used in the synthesis of bioactive molecules and drug candidates.

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