(3-((4-Hydroxypiperidin-1-yl)sulfonyl)phenyl)boronic acid

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Reagent Code: #65443
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CAS Number 1704063-58-0

science Other reagents with same CAS 1704063-58-0

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scatter_plot Molecular Information
Weight 285.13 g/mol
Formula C₁₁H₁₆BNO₅S
badge Registry Numbers
MDL Number MFCD28384263
inventory_2 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 biologically active compounds, particularly in the creation of inhibitors targeting specific enzymes or receptors. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in drug discovery and material science. Additionally, its sulfonyl and hydroxypiperidinyl groups contribute to its potential in designing molecules with improved solubility and binding affinity, making it useful in the optimization of drug candidates for therapeutic applications.

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inventory 1g
10-20 days ฿44,770.00

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(3-((4-Hydroxypiperidin-1-yl)sulfonyl)phenyl)boronic acid
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This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of biologically active compounds, particularly in the creation of inhibitors targeting specific enzymes or receptors. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in drug discovery and material science. Additionally, its sulfonyl and hydroxypiperidinyl groups contribute to its p

This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of biologically active compounds, particularly in the creation of inhibitors targeting specific enzymes or receptors. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in drug discovery and material science. Additionally, its sulfonyl and hydroxypiperidinyl groups contribute to its potential in designing molecules with improved solubility and binding affinity, making it useful in the optimization of drug candidates for therapeutic applications.

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