2-Chloro-3-Cyanopyridine-4-Boronic Acid Pinacol Ester

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Reagent Code: #165901
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CAS Number 878194-94-6

science Other reagents with same CAS 878194-94-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.52 g/mol
Formula C₁₂H₁₄BClN₂O₂
badge Registry Numbers
MDL Number MFCD09037479
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry

description Product Description

Used as a key intermediate in pharmaceutical synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of active pharmaceutical ingredients (APIs). Commonly applied in the production of kinase inhibitors and other nitrogen-containing heterocyclic drugs. The presence of both cyano and chloro functionalities allows for further derivatization, enhancing its utility in drug discovery and medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,870.00
inventory 1g
10-20 days ฿27,690.00

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2-Chloro-3-Cyanopyridine-4-Boronic Acid Pinacol Ester
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Used as a key intermediate in pharmaceutical synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of active pharmaceutical ingredients (APIs). Commonly applied in the production of kinase inhibitors and other nitrogen-containing heterocyclic drugs. The presence of both cyano and chloro functionalities allows for further derivatization,

Used as a key intermediate in pharmaceutical synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of active pharmaceutical ingredients (APIs). Commonly applied in the production of kinase inhibitors and other nitrogen-containing heterocyclic drugs. The presence of both cyano and chloro functionalities allows for further derivatization, enhancing its utility in drug discovery and medicinal chemistry research.

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