4-hydroxy-2-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde

97%(HPLC)

Reagent Code: #46699
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CAS Number 1883607-86-0

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.08 g/mol
Formula C₁₃H₁₇BO₄
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various boron-containing molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The boronate ester group in the compound facilitates the formation of carbon-carbon bonds, enabling the construction of complex organic structures. Additionally, it serves as a precursor in the development of fluorescent probes and sensors, leveraging its aldehyde functionality for further derivatization. Its stability and reactivity make it a versatile tool in medicinal chemistry for designing drug candidates and bioactive molecules.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿9,000.00

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4-hydroxy-2-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
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This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various boron-containing molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The boronate ester group in the compound facilitates the formation of carbon-carbon bonds, enabling the construction of complex organic structures. Additionally, it serves as a precursor in the dev

This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various boron-containing molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The boronate ester group in the compound facilitates the formation of carbon-carbon bonds, enabling the construction of complex organic structures. Additionally, it serves as a precursor in the development of fluorescent probes and sensors, leveraging its aldehyde functionality for further derivatization. Its stability and reactivity make it a versatile tool in medicinal chemistry for designing drug candidates and bioactive molecules.

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