(5-Cyano-2-(methoxymethoxy)phenyl)boronic acid

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Reagent Code: #165900
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CAS Number 1256345-61-5

science Other reagents with same CAS 1256345-61-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.99 g/mol
Formula C₉H₁₀BNO₄
badge Registry Numbers
MDL Number MFCD17015728
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid functionality enables efficient carbon-carbon bond formation under mild conditions. The methoxymethoxy group acts as a protecting group, allowing selective reactivity at other sites during multi-step syntheses. Commonly employed in the preparation of biaryl compounds and functionalized aromatic systems found in bioactive molecules. Its cyano group can be further modified to introduce amines, carboxylic acids, or heterocycles, expanding its utility in drug discovery and materials science.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,790.00
inventory 1g
10-20 days ฿23,480.00

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(5-Cyano-2-(methoxymethoxy)phenyl)boronic acid
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid functionality enables efficient carbon-carbon bond formation under mild conditions. The methoxymethoxy group acts as a protecting group, allowing selective reactivity at other sites during multi-step syntheses. Commonly employed in the preparation of biaryl compounds and functionalized aromatic systems found in bio

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic acid functionality enables efficient carbon-carbon bond formation under mild conditions. The methoxymethoxy group acts as a protecting group, allowing selective reactivity at other sites during multi-step syntheses. Commonly employed in the preparation of biaryl compounds and functionalized aromatic systems found in bioactive molecules. Its cyano group can be further modified to introduce amines, carboxylic acids, or heterocycles, expanding its utility in drug discovery and materials science.

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