(3-Phenoxyphenyl)boronic acid
98%
Reagent
Code: #86056
CAS Number
221006-66-2
blur_circular Chemical Specifications
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Molecular Information
Weight
214.02 g/mol
Formula
C₁₂H₁₁BO₃
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Registry Numbers
MDL Number
MFCD07780272
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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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(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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