4-(4-Fluorophenyl)phenylboronic acid

≥98%

Reagent Code: #90460
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CAS Number 140369-67-1

science Other reagents with same CAS 140369-67-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.02 g/mol
Formula C₁₂H₁₀BFO₂
thermostat Physical Properties
Boiling Point 382.309ºC
inventory_2 Storage & Handling
Density 1.257 g/cm3
Storage room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. This compound is also employed in the production of advanced materials, such as organic semiconductors and liquid crystals, due to its ability to modify electronic properties. Additionally, it serves as a building block in the creation of bioactive compounds for research in medicinal chemistry. Its applications extend to the field of chemical sensors, where it aids in the detection of specific analytes.

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Test Parameter Specification
Appearance Solid
Purity (%) 98-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿495.00
inventory 1g
10-20 days ฿1,143.00

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4-(4-Fluorophenyl)phenylboronic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. This compound is also employed in the production of advanced materials, such as organic semiconductors and liquid crystals, due to its ability to modify electronic properties. Additionally, it serves as a building bl

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. This compound is also employed in the production of advanced materials, such as organic semiconductors and liquid crystals, due to its ability to modify electronic properties. Additionally, it serves as a building block in the creation of bioactive compounds for research in medicinal chemistry. Its applications extend to the field of chemical sensors, where it aids in the detection of specific analytes.

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