4-(2-(4-(tert-Butoxycarbonyl)piperazin-1-yl)ethoxy)-3-fluorophenylboronic acid
98%
Reagent
Code: #90332
CAS Number
1704064-14-1
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Molecular Information
Weight
368.22 g/mol
Formula
C₁₇H₂₆BFN₂O₅
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Registry Numbers
MDL Number
MFCD28400177
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Storage & Handling
Storage
2-8°C
description Product Description
This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of biologically active molecules, particularly in the synthesis of protease inhibitors and other therapeutic agents. The boronic acid group enables its use in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds in drug discovery. The tert-butoxycarbonyl (Boc) protecting group on the piperazine moiety allows for selective deprotection and further functionalization, making it valuable in constructing complex molecular architectures. Its applications are particularly relevant in medicinal chemistry for designing and optimizing drug candidates targeting various diseases.
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4-(2-(4-(tert-Butoxycarbonyl)piperazin-1-yl)ethoxy)-3-fluorophenylboronic acid
This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of biologically active molecules, particularly in the synthesis of protease inhibitors and other therapeutic agents. The boronic acid group enables its use in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds in drug discovery. The tert-butoxycarbonyl (Boc) protecting group on the piperazine moiety allows for selective deprotection and further functionalization, making it valuable in constructing complex molecular architectures. Its applications are particularly relevant in medicinal chemistry for designing and optimizing drug candidates targeting various diseases.
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