(4-((dimethylamino)methyl)-3-fluorophenyl)boronic acid
98%
Reagent
Code: #90315
CAS Number
1334173-89-5
blur_circular Chemical Specifications
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Molecular Information
Weight
197.02 g/mol
Formula
C₉H₁₃BFNO₂
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Registry Numbers
MDL Number
MFCD14687171
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Storage & Handling
Storage
2-8°C
description Product Description
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, enabling the creation of complex organic molecules. Its boronic acid group acts as a key reactant, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. This makes it valuable in the pharmaceutical industry for synthesizing drug intermediates and active pharmaceutical ingredients (APIs). Additionally, it is used in materials science for developing advanced polymers and organic electronic materials, where precise molecular architecture is required. Its fluorinated aromatic structure also enhances its stability and reactivity in various chemical processes.
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(4-((dimethylamino)methyl)-3-fluorophenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, enabling the creation of complex organic molecules. Its boronic acid group acts as a key reactant, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. This makes it valuable in the pharmaceutical industry for synthesizing drug intermediates and active pharmaceutical ingredients (APIs). Additionally, it is used in materials science for developing advanced polymers and organic electronic materials, where precise molecular architecture is required. Its fluorinated aromatic structure also enhances its stability and reactivity in various chemical processes.
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