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

95%

Reagent Code: #92318
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CAS Number 2225155-30-4

science Other reagents with same CAS 2225155-30-4

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Weight 223.42408 g/mol
Formula C₈H₇BClN₃O₂
inventory_2 Storage & Handling
Storage -20℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to create complex organic molecules. Its boronic acid group allows for efficient coupling with aryl halides, making it valuable in medicinal chemistry for designing targeted therapies. Additionally, it is employed in the production of agrochemicals and materials science for creating advanced functional compounds.

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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-(1H-pyrazol-1-yl)pyridine-3-boronic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to create complex organic molecules. Its boronic acid group allows for efficient coupling with aryl halides, making it valuable in medicinal chemistry for designing targeted therapies. Additionally, it is employed in the production of agrochemicals and mat

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to create complex organic molecules. Its boronic acid group allows for efficient coupling with aryl halides, making it valuable in medicinal chemistry for designing targeted therapies. Additionally, it is employed in the production of agrochemicals and materials science for creating advanced functional compounds.

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