(3-(p-Tolylcarbamoyl)phenyl)boronic acid

95%

Reagent Code: #242010
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CAS Number 1072946-03-2

science Other reagents with same CAS 1072946-03-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.08 g/mol
Formula C₁₄H₁₄BNO₃
badge Registry Numbers
MDL Number MFCD10699620
inventory_2 Storage & Handling
Storage 2-8°C, inert atmosphere

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 pharmaceutical and agrochemical development. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and materials science. The presence of a carbamoyl group adds polarity and hydrogen bonding capability, which can influence the biological activity and solubility of target molecules. Commonly employed in the preparation of bioactive molecules and conjugated systems for optoelectronic applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,500.00
inventory 5g
10-20 days ฿12,600.00
inventory 25g
10-20 days ฿41,200.00

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(3-(p-Tolylcarbamoyl)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 pharmaceutical and agrochemical development. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and materials science. The presence of a carbamoyl group adds polarity and hydrogen bonding capability, which can influence the biological activity and solubility of target molecules. Commonly

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl compounds important in pharmaceutical and agrochemical development. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and materials science. The presence of a carbamoyl group adds polarity and hydrogen bonding capability, which can influence the biological activity and solubility of target molecules. Commonly employed in the preparation of bioactive molecules and conjugated systems for optoelectronic applications.

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