4-Chloro-2-(1H-pyrazol-1-yl)phenylboronic acid

95%

Reagent Code: #60876
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CAS Number 2225155-80-4

science Other reagents with same CAS 2225155-80-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.43602 g/mol
Formula C₉H₈BClN₂O₂
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex organic molecules, especially in pharmaceuticals and agrochemicals. Its boronic acid group enables efficient formation of carbon-carbon bonds, making it valuable in drug discovery and material science. Additionally, it is utilized in the development of biologically active compounds, including potential therapeutic agents targeting specific enzymes or receptors. Its pyrazole moiety further enhances its utility in designing molecules with diverse biological activities.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿16,182.00
inventory 25mg
10-20 days ฿46,782.00

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4-Chloro-2-(1H-pyrazol-1-yl)phenylboronic acid
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This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex organic molecules, especially in pharmaceuticals and agrochemicals. Its boronic acid group enables efficient formation of carbon-carbon bonds, making it valuable in drug discovery and material science. Additionally, it is utilized in the development of biologically active compounds, including potential therapeutic agents targ

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex organic molecules, especially in pharmaceuticals and agrochemicals. Its boronic acid group enables efficient formation of carbon-carbon bonds, making it valuable in drug discovery and material science. Additionally, it is utilized in the development of biologically active compounds, including potential therapeutic agents targeting specific enzymes or receptors. Its pyrazole moiety further enhances its utility in designing molecules with diverse biological activities.

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