4-Chloro-3-(cyclopropylcarbamoyl)phenylboronic acid

98%

Reagent Code: #90635
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CAS Number 871332-73-9

science Other reagents with same CAS 871332-73-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.46 g/mol
Formula C₁₀H₁₁BClNO₃
badge Registry Numbers
MDL Number MFCD07783865
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals, particularly in the development of kinase inhibitors. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex molecules. This compound is also employed in the synthesis of bioactive compounds targeting cancer and inflammatory diseases. Its boronic acid group facilitates interactions with biological targets, making it valuable in drug discovery and medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿12,699.00
inventory 1g
10-20 days ฿31,734.00

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4-Chloro-3-(cyclopropylcarbamoyl)phenylboronic acid
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Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals, particularly in the development of kinase inhibitors. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex molecules. This compound is also employed in the synthesis of bioactive compounds targeting cancer and inflammatory diseases. Its boronic acid group facilitates interactions with biological targets, making it valuable in drug discover

Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals, particularly in the development of kinase inhibitors. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex molecules. This compound is also employed in the synthesis of bioactive compounds targeting cancer and inflammatory diseases. Its boronic acid group facilitates interactions with biological targets, making it valuable in drug discovery and medicinal chemistry research.

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