(3-(tert-Butoxymethyl)-4-fluorophenyl)boronic acid

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Reagent Code: #65511
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CAS Number 1704067-02-6

science Other reagents with same CAS 1704067-02-6

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Weight 226.06 g/mol
Formula C₁₁H₁₆BFO₃
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MDL Number MFCD28384220
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The boronic acid group enables the formation of carbon-carbon bonds, making it valuable in constructing biaryl structures. Its tert-butoxymethyl and fluorine substituents enhance its stability and reactivity, allowing for selective transformations in multi-step synthetic processes. Additionally, it is employed in the development of bioactive compounds, where the fluorine atom can improve metabolic stability and binding affinity in drug candidates.

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inventory 1g
10-20 days ฿33,190.00

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(3-(tert-Butoxymethyl)-4-fluorophenyl)boronic acid
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This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The boronic acid group enables the formation of carbon-carbon bonds, making it valuable in constructing biaryl structures. Its tert-butoxymethyl and fluorine substituents enhance its stability and reactivity, allowing for selective transformations in multi-step synthetic p

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The boronic acid group enables the formation of carbon-carbon bonds, making it valuable in constructing biaryl structures. Its tert-butoxymethyl and fluorine substituents enhance its stability and reactivity, allowing for selective transformations in multi-step synthetic processes. Additionally, it is employed in the development of bioactive compounds, where the fluorine atom can improve metabolic stability and binding affinity in drug candidates.

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