4-Fluoro-3-methylphenylboronic acid
99%
Reagent
Code: #90604
Alias
4-fluoro-3-methylphenylboronic acid
CAS Number
139911-27-6
blur_circular Chemical Specifications
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Molecular Information
Weight
153.95 g/mol
Formula
C₇H₈BFO₂
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Registry Numbers
MDL Number
MFCD01863527
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Physical Properties
Melting Point
212-217 °C(lit.)
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Storage & Handling
Storage
room temperature, dry
description Product Description
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug development. Additionally, it is employed in the preparation of advanced materials and organic electronic components due to its ability to modify molecular structures effectively. Its fluorine substituent enhances its reactivity and stability, making it a valuable building block in various chemical processes.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Melting point | 216-218 |
Purity (HPLC) | 99-100% |
Purity (Neutralization Titration) | 98.5-101.5% |
Appearance | White to off-white powder |
Infrared Spectrum | Conforms to Structure |
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4-Fluoro-3-methylphenylboronic acid
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug development. Additionally, it is employed in the preparation of advanced materials and organic electronic components due to its ability to modify molecular structures effectively. Its fluorine substituent enhances its reactivity and stability, making it a valuable building block in various chemical processes.
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