(3-Phenoxyphenyl)boronic acid

98%

Reagent Code: #86056
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CAS Number 221006-66-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.02 g/mol
Formula C₁₂H₁₁BO₃
badge Registry Numbers
MDL Number MFCD07780272
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

(3-Phenoxyphenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of diverse aromatic structures. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with diols and other biomolecules. Its applications extend to materials science, where it contributes to the design of organic electronic devices and functional coatings.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days £23.45
inventory 1g
10-20 days £58.21
inventory 5g
10-20 days £203.02
(3-Phenoxyphenyl)boronic acid
(3-Phenoxyphenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of diverse aromatic structures. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with diols and other biomolecules. Its applications extend to materials science, where it contributes to the design of organic electronic devices and functional coatings.
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