(4-Chloro-3-(4-ethylpiperazine-1-carbonyl)phenyl)boronic acid

98%

Reagent Code: #89302
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CAS Number 1704074-11-2

science Other reagents with same CAS 1704074-11-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.56 g/mol
Formula C₁₃H₁₈BClN₂O₃
badge Registry Numbers
MDL Number MFCD28384313
inventory_2 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 various biologically active molecules, particularly in the synthesis of protease inhibitors and other therapeutic agents. 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 structure, featuring both a piperazine moiety and a boronic acid group, enhances its potential in targeting enzymes and receptors involved in disease pathways, making it a promising candidate for medicinal chemistry applications.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿13,980.00
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(4-Chloro-3-(4-ethylpiperazine-1-carbonyl)phenyl)boronic acid
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This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly in the synthesis of protease inhibitors and other therapeutic agents. 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 structure, featuring both a piperazine moiety and a

This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly in the synthesis of protease inhibitors and other therapeutic agents. 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 structure, featuring both a piperazine moiety and a boronic acid group, enhances its potential in targeting enzymes and receptors involved in disease pathways, making it a promising candidate for medicinal chemistry applications.

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