4-(Trifluoromethyl)phenylboronic acid
98%
Reagent
Code: #90520
Alias
4-(Trifluoromethyl)phenylboronic acid ;4-Trifluoromethylphenylboronic acid, p-trifluoromethylphenylboronic acid
CAS Number
128796-39-4
blur_circular Chemical Specifications
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Molecular Information
Weight
189.93 g/mol
Formula
C₇H₆BF₃O₂
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Registry Numbers
MDL Number
MFCD00151855
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Physical Properties
Melting Point
245-250 °C(lit.)
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Storage & Handling
Storage
2~8°C
description Product Description
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create biaryl structures, which are essential in pharmaceuticals, agrochemicals, and materials science. Its trifluoromethyl group enhances the reactivity and stability of the resulting products, making it valuable in drug discovery for developing compounds with improved metabolic stability and bioavailability. Additionally, it serves as a building block in the synthesis of advanced materials, such as liquid crystals and polymers, due to its ability to introduce fluorine atoms into the molecular structure, which can alter physical and chemical properties.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity (HPLC) | 98-100% |
Appearance | White to off-white powder or solid |
Infrared Spectrum | Conforms to Structure |
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4-(Trifluoromethyl)phenylboronic acid
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create biaryl structures, which are essential in pharmaceuticals, agrochemicals, and materials science. Its trifluoromethyl group enhances the reactivity and stability of the resulting products, making it valuable in drug discovery for developing compounds with improved metabolic stability and bioavailability. Additionally, it serves as a building block in the synthesis of advanced materials, such as liquid crystals and polymers, due to its ability to introduce fluorine atoms into the molecular structure, which can alter physical and chemical properties.
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