(4-(1-Methyl-1H-imidazol-2-yl)phenyl)boronic acid

97%

Reagent Code: #209085
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CAS Number 1310383-27-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.02 g/mol
Formula C₁₀H₁₁BN₂O₂
badge Registry Numbers
MDL Number MFCD11111510
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct biaryl compounds which are common scaffolds in pharmaceuticals and agrochemicals. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of drug candidates involving imidazole and aromatic ring systems, especially in medicinal chemistry research targeting kinase inhibitors and bioactive molecules. Also utilized in the synthesis of fluorescent probes and functional materials due to its stable boronate ester formation and compatibility with diverse reaction conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days $327.00
inventory 250mg
10-20 days $571.05
inventory 1g
10-20 days $1,427.23
(4-(1-Methyl-1H-imidazol-2-yl)phenyl)boronic acid
Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct biaryl compounds which are common scaffolds in pharmaceuticals and agrochemicals. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of drug candidates involving imidazole and aromatic ring systems, especially in medicinal chemistry research targeting kinase inhibitors and bioactive molecules. Also utilized in the synthesis of fluorescent probes and functional materials due to its stable boronate ester formation and compatibility with diverse reaction conditions.
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