(4-Formyl-3-methoxyphenyl)boronic acid

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Reagent Code: #90706
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CAS Number 815620-00-9

science Other reagents with same CAS 815620-00-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.97 g/mol
Formula C₈H₉BO₄
badge Registry Numbers
MDL Number MFCD10697427
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and bioactive compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, enabling the synthesis of complex molecules. This compound is also employed in the development of sensors and probes due to its boronic acid group, which can selectively bind to diols and sugars, making it useful in glucose sensing and other biochemical applications. Additionally, it serves as a building block in material science for creating advanced polymers and functional materials.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,742.00
inventory 1g
10-20 days ฿11,511.00
inventory 5g
10-20 days ฿34,686.00

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(4-Formyl-3-methoxyphenyl)boronic acid
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Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and bioactive compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, enabling the synthesis of complex molecules. This compound is also employed in the development of sensors and probes due to its boronic acid group, which can selectively bind to diols and sugars, making it useful in glucose sensing and other biochemical appl

Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and bioactive compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, enabling the synthesis of complex molecules. This compound is also employed in the development of sensors and probes due to its boronic acid group, which can selectively bind to diols and sugars, making it useful in glucose sensing and other biochemical applications. Additionally, it serves as a building block in material science for creating advanced polymers and functional materials.

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