5-Chloro-6-(3-methyl-1H-pyrazol-1-yl)pyridine-3-boronic acid

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Reagent Code: #92335
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CAS Number 2225173-74-8

science Other reagents with same CAS 2225173-74-8

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Weight 237.45066 g/mol
Formula C₉H₉BClN₃O₂
inventory_2 Storage & Handling
Storage -20℃

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds, which is essential in the construction of complex organic molecules. Its pyridine and pyrazole moieties make it a valuable building block in the development of pharmaceuticals, agrochemicals, and materials science. The compound's structure allows for the introduction of specific functional groups, enhancing its utility in designing biologically active compounds, including potential drug candidates. Additionally, it is employed in the synthesis of heterocyclic compounds, which are often used in medicinal chemistry for their diverse pharmacological properties.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿12,492.00
inventory 25mg
10-20 days ฿29,592.00

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5-Chloro-6-(3-methyl-1H-pyrazol-1-yl)pyridine-3-boronic acid
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds, which is essential in the construction of complex organic molecules. Its pyridine and pyrazole moieties make it a valuable building block in the development of pharmaceuticals, agrochemicals, and materials science. The compound's structure allows for the introduction of specific functiona

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds, which is essential in the construction of complex organic molecules. Its pyridine and pyrazole moieties make it a valuable building block in the development of pharmaceuticals, agrochemicals, and materials science. The compound's structure allows for the introduction of specific functional groups, enhancing its utility in designing biologically active compounds, including potential drug candidates. Additionally, it is employed in the synthesis of heterocyclic compounds, which are often used in medicinal chemistry for their diverse pharmacological properties.

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