(4-Hydroxy-3-methoxyphenyl)boronic acid

≥95%

Reagent Code: #113326
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CAS Number 182344-21-4

science Other reagents with same CAS 182344-21-4

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scatter_plot Molecular Information
Weight 167.96 g/mol
Formula C₇H₉BO₄
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MDL Number MFCD18397223
inventory_2 Storage & Handling
Storage -20°C, store under inert gas

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create biaryl compounds, which are important in pharmaceuticals and materials science. Acts as a key intermediate in the production of complex molecules, including drugs and agrochemicals. Also employed in the development of sensors and diagnostic tools due to its ability to bind with diols and sugars, making it useful in glucose detection and other biochemical applications. Its boronic acid group facilitates the formation of stable complexes, enhancing its utility in various chemical and biological processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,655.00
inventory 100mg
10-20 days ฿1,845.00
inventory 1g
10-20 days ฿7,488.00

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(4-Hydroxy-3-methoxyphenyl)boronic acid
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create biaryl compounds, which are important in pharmaceuticals and materials science. Acts as a key intermediate in the production of complex molecules, including drugs and agrochemicals. Also employed in the development of sensors and diagnostic tools due to its ability to bind with diols and sugars, making it useful in glucose detection and other biochemical applications. Its boronic acid group facilitates the forma

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create biaryl compounds, which are important in pharmaceuticals and materials science. Acts as a key intermediate in the production of complex molecules, including drugs and agrochemicals. Also employed in the development of sensors and diagnostic tools due to its ability to bind with diols and sugars, making it useful in glucose detection and other biochemical applications. Its boronic acid group facilitates the formation of stable complexes, enhancing its utility in various chemical and biological processes.

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