(4-(Pyridin-2-ylcarbamoyl)phenyl)boronic acid

97%

Reagent Code: #226330
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CAS Number 850568-25-1

science Other reagents with same CAS 850568-25-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.04 g/mol
Formula C₁₂H₁₁BN₂O₃
badge Registry Numbers
MDL Number MFCD06659876
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl compounds important in pharmaceuticals and agrochemicals. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions. Commonly employed in the development of kinase inhibitors and other bioactive molecules due to the presence of the pyridine and carbamoyl functionalities, which enhance binding to biological targets. Also applied in materials science for constructing conjugated systems in optoelectronic materials.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿3,980.00
1g
10-20 days ฿11,000.00
5g
10-20 days ฿38,600.00
25g
10-20 days ฿175,880.00
(4-(Pyridin-2-ylcarbamoyl)phenyl)boronic acid
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Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl compounds important in pharmaceuticals and agrochemicals. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions. Commonly employed in the development of kinase inhibitors and other bioactive molecules due to the presence of the pyridine and carbamoyl functionalities, which enhance binding to biological targets. Also applied in materials science for co

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl compounds important in pharmaceuticals and agrochemicals. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions. Commonly employed in the development of kinase inhibitors and other bioactive molecules due to the presence of the pyridine and carbamoyl functionalities, which enhance binding to biological targets. Also applied in materials science for constructing conjugated systems in optoelectronic materials.

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