(5-Methoxy-[1,1'-biphenyl]-3-yl)boronic acid

95%

Reagent Code: #113349
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CAS Number 1111181-69-1

science Other reagents with same CAS 1111181-69-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.05 g/mol
Formula C₁₃H₁₃BO₃
badge Registry Numbers
MDL Number MFCD28167233
thermostat Physical Properties
Boiling Point 442.2±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.20±0.1 g/cm3(Predicted)
Storage Room temperature, dark, inert gas

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a crucial building block 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, facilitating the creation of carbon-carbon bonds. Additionally, it is employed in the development of bioactive molecules and intermediates for drug discovery, where its biphenyl moiety contributes to the desired pharmacological properties. Its stability and reactivity make it a valuable reagent in medicinal chemistry and material science research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,470.00
inventory 1g
10-20 days ฿34,272.00
inventory 250mg
10-20 days ฿12,699.00

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(5-Methoxy-[1,1'-biphenyl]-3-yl)boronic acid
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a crucial building block 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, facilitating the creation of carbon-carbon bonds. Additionally, it is employed in the development of bioactive molecules and intermediates

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a crucial building block 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, facilitating the creation of carbon-carbon bonds. Additionally, it is employed in the development of bioactive molecules and intermediates for drug discovery, where its biphenyl moiety contributes to the desired pharmacological properties. Its stability and reactivity make it a valuable reagent in medicinal chemistry and material science research.

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