4-(2,2,2-Trifluoroethoxy)phenylboronic Acid
97%
Reagent
Code: #90330
CAS Number
886536-37-4
blur_circular Chemical Specifications
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Molecular Information
Weight
219.95 g/mol
Formula
C₈H₈BF₃O₃
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Registry Numbers
MDL Number
MFCD09027239
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Physical Properties
Melting Point
191-194°C
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Storage & Handling
Storage
room temperature
description Product Description
This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and materials science research. Additionally, it is employed in the development of bioactive compounds and advanced materials due to its stability and reactivity. Its trifluoroethoxy group can also impart unique electronic properties to the resulting products, enhancing their functionality in specific applications.
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4-(2,2,2-Trifluoroethoxy)phenylboronic Acid
This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and materials science research. Additionally, it is employed in the development of bioactive compounds and advanced materials due to its stability and reactivity. Its trifluoroethoxy group can also impart unique electronic properties to the resulting products, enhancing their functionality in specific applications.
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