4-(2-(4-Ethylpiperazin-1-yl)ethoxy)-3-fluorophenylboronic acid
98%
Reagent
Code: #90333
CAS Number
1704064-13-0
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Molecular Information
Weight
296.15 g/mol
Formula
C₁₄H₂₂BFN₂O₃
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Registry Numbers
MDL Number
MFCD28400176
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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. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable for constructing complex organic molecules, such as pharmaceuticals and agrochemicals. The ethylpiperazine moiety enhances its solubility and reactivity in various solvents, facilitating its use in diverse reaction conditions. Additionally, the fluorine atom can influence the electronic properties of the molecule, aiding in the development of compounds with specific biological activities. Its application is particularly significant in the synthesis of drug intermediates and active pharmaceutical ingredients (APIs), where precise molecular structures are crucial.
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4-(2-(4-Ethylpiperazin-1-yl)ethoxy)-3-fluorophenylboronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable for constructing complex organic molecules, such as pharmaceuticals and agrochemicals. The ethylpiperazine moiety enhances its solubility and reactivity in various solvents, facilitating its use in diverse reaction conditions. Additionally, the fluorine atom can influence the electronic properties of the molecule, aiding in the development of compounds with specific biological activities. Its application is particularly significant in the synthesis of drug intermediates and active pharmaceutical ingredients (APIs), where precise molecular structures are crucial.
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