(3-Chloro-5-cyanophenyl)boronic acid

98%

Reagent Code: #90216
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CAS Number 915763-60-9

science Other reagents with same CAS 915763-60-9

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Weight 181.38 g/mol
Formula C₇H₅BClNO₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

(3-Chloro-5-cyanophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the coupling of aryl or vinyl halides with arylboronic acids to create complex organic molecules. Additionally, it is employed in the development of bioactive compounds and in medicinal chemistry research for designing drug candidates. Its unique structure, combining chloro and cyano groups, also makes it useful in the synthesis of specialized polymers and functional materials.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿738.00
inventory 250mg
10-20 days ฿2,376.00

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(3-Chloro-5-cyanophenyl)boronic acid
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(3-Chloro-5-cyanophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the coupling of aryl or vinyl halides with arylboronic acids to create complex organic molecules. Additionally, it is employed in the development of bioactive com

(3-Chloro-5-cyanophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the coupling of aryl or vinyl halides with arylboronic acids to create complex organic molecules. Additionally, it is employed in the development of bioactive compounds and in medicinal chemistry research for designing drug candidates. Its unique structure, combining chloro and cyano groups, also makes it useful in the synthesis of specialized polymers and functional materials.

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