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

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Reagent Code: #90865
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CAS Number 2225175-34-6

science Other reagents with same CAS 2225175-34-6

blur_circular Chemical Specifications

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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 Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in constructing complex organic molecules, such as active pharmaceutical ingredients (APIs) and biologically active compounds. Additionally, it is employed in the development of organic electronic materials and polymers, contributing to advancements in materials science. Its stability and reactivity make it a versatile tool in medicinal chemistry and industrial applications.

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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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5-Chloro-2-(1H-pyrazol-1-yl)phenylboronic acid
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This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in constructing complex organic molecules, such as active pharmaceutical ingredients (APIs) and biologically active compounds. Additionally, it is

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in constructing complex organic molecules, such as active pharmaceutical ingredients (APIs) and biologically active compounds. Additionally, it is employed in the development of organic electronic materials and polymers, contributing to advancements in materials science. Its stability and reactivity make it a versatile tool in medicinal chemistry and industrial applications.

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