3-Fluoro-4-formylphenylboronic acid
98%
Reagent
Code: #90163
Alias
3-Fluoro-4-formylphenylboronic acid
CAS Number
248270-25-9
blur_circular Chemical Specifications
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Molecular Information
Weight
167.93 g/mol
Formula
C₇H₆BFO₃
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Registry Numbers
MDL Number
MFCD02093051
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Physical Properties
Melting Point
249-250°C
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Storage & Handling
Storage
room temperature, dry
description Product Description
Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to create complex molecules. Its boronic acid group facilitates the coupling with aryl halides, making it valuable in drug discovery and development. Additionally, it is employed in the synthesis of fluorescent probes and sensors due to its ability to interact with specific biological targets. Its formyl group allows for further functionalization, enhancing its versatility in designing advanced materials and bioactive compounds.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity (Neutralization Titration) | 97.5-102.5% |
Appearance | White to tan powder, crystals, and/or chunks |
Infrared Spectrum | Conforms to Structure |
Proton NMR Spectrum | Conforms to Structure |
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3-Fluoro-4-formylphenylboronic acid
Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to create complex molecules. Its boronic acid group facilitates the coupling with aryl halides, making it valuable in drug discovery and development. Additionally, it is employed in the synthesis of fluorescent probes and sensors due to its ability to interact with specific biological targets. Its formyl group allows for further functionalization, enhancing its versatility in designing advanced materials and bioactive compounds.
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