(4-(1-Phenyl-1H-benzo[d]imidazol-2-yl)phenyl)boronic acid

99%

Reagent Code: #224340
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CAS Number 952514-79-3

science Other reagents with same CAS 952514-79-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 314.1500 g/mol
Formula C₁₉H₁₅BN₂O₂
badge Registry Numbers
MDL Number MFCD11045057
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used in organic synthesis as a key building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl compounds important in pharmaceuticals and agrochemicals. Its boronic acid functionality allows for efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of fluorescent materials and sensors due to the presence of the benzimidazole moiety, which can act as a signaling unit. Also utilized in medicinal chemistry for constructing libraries of bioactive molecules, particularly those targeting kinase inhibitors and anticancer agents. Its structural rigidity and ability to participate in hydrogen bonding make it suitable for designing compounds with enhanced binding affinity and selectivity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,240.00
5g
10-20 days ฿4,830.00
(4-(1-Phenyl-1H-benzo[d]imidazol-2-yl)phenyl)boronic acid
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Used in organic synthesis as a key building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl compounds important in pharmaceuticals and agrochemicals. Its boronic acid functionality allows for efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of fluorescent materials and sensors due to the presence of the benzimidazole moiety, which can act as a signaling unit. Also utilized in medicinal chemistry for constructing librari

Used in organic synthesis as a key building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl compounds important in pharmaceuticals and agrochemicals. Its boronic acid functionality allows for efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of fluorescent materials and sensors due to the presence of the benzimidazole moiety, which can act as a signaling unit. Also utilized in medicinal chemistry for constructing libraries of bioactive molecules, particularly those targeting kinase inhibitors and anticancer agents. Its structural rigidity and ability to participate in hydrogen bonding make it suitable for designing compounds with enhanced binding affinity and selectivity.

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