4-(4-(tert-Butoxycarbonyl)piperazin-1-ylsulfonyl)phenylboronic acid
98%
Reagent
Code: #90418
CAS Number
486422-54-2
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Molecular Information
Weight
370.24 g/mol
Formula
C₁₅H₂₃BN₂O₆S
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Registry Numbers
MDL Number
MFCD28384269
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Storage & Handling
Storage
2-8°C
description Product Description
This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly those targeting protease enzymes. The tert-butoxycarbonyl (Boc) protecting group ensures stability during synthetic processes, while the boronic acid moiety enables participation in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. Its sulfonyl group enhances reactivity and selectivity, making it valuable in constructing complex molecular architectures. Applications include the synthesis of drug candidates for diseases such as cancer, inflammation, and infectious diseases. Additionally, it is employed in the preparation of advanced materials and ligands for catalysis.
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4-(4-(tert-Butoxycarbonyl)piperazin-1-ylsulfonyl)phenylboronic acid
This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly those targeting protease enzymes. The tert-butoxycarbonyl (Boc) protecting group ensures stability during synthetic processes, while the boronic acid moiety enables participation in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. Its sulfonyl group enhances reactivity and selectivity, making it valuable in constructing complex molecular architectures. Applications include the synthesis of drug candidates for diseases such as cancer, inflammation, and infectious diseases. Additionally, it is employed in the preparation of advanced materials and ligands for catalysis.
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