4-(2-(tert-Butoxycarbonyl(cyclopropyl)amino)ethoxy)-3-fluorophenylboronic acid
98%
Reagent
Code: #90336
CAS Number
1704064-17-4
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Molecular Information
Weight
339.17 g/mol
Formula
C₁₆H₂₃BFNO₅
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Registry Numbers
MDL Number
MFCD28400180
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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 in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butoxycarbonyl (Boc) protecting group ensures stability during reactions, while the cyclopropyl and fluorine substituents can influence the electronic and steric properties of the resulting products. This chemical is often employed in the development of biologically active compounds, where its structural features contribute to enhanced selectivity and efficacy.
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4-(2-(tert-Butoxycarbonyl(cyclopropyl)amino)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 in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butoxycarbonyl (Boc) protecting group ensures stability during reactions, while the cyclopropyl and fluorine substituents can influence the electronic and steric properties of the resulting products. This chemical is often employed in the development of biologically active compounds, where its structural features contribute to enhanced selectivity and efficacy.
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