(4-((4-Chlorobenzyl)oxy)phenyl)boronic acid

95%

Reagent Code: #166803
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CAS Number 870778-91-9

science Other reagents with same CAS 870778-91-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.50 g/mol
Formula C₁₃H₁₂BClO₃
badge Registry Numbers
MDL Number MFCD07784349
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates coupling with aryl halides, making it valuable in creating biaryl compounds for drug discovery and materials science. The presence of a chlorobenzyl ether moiety adds structural diversity, useful in designing bioactive molecules. Commonly employed in research settings for the synthesis of potential therapeutic agents and functional organic materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,940.00
inventory 250mg
10-20 days ฿3,180.00
inventory 1g
10-20 days ฿8,120.00
inventory 25g
10-20 days ฿99,370.00
inventory 5g
10-20 days ฿27,210.00

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(4-((4-Chlorobenzyl)oxy)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 carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates coupling with aryl halides, making it valuable in creating biaryl compounds for drug discovery and materials science. The presence of a chlorobenzyl ether moiety adds structural diversity, useful in designing bioactive molecules. Commonly employed in research settings for the synthesis of

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates coupling with aryl halides, making it valuable in creating biaryl compounds for drug discovery and materials science. The presence of a chlorobenzyl ether moiety adds structural diversity, useful in designing bioactive molecules. Commonly employed in research settings for the synthesis of potential therapeutic agents and functional organic materials.

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