(3-Formyl-5-methylphenyl)boronic acid

98%

Reagent Code: #90257
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CAS Number 870777-33-6

science Other reagents with same CAS 870777-33-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.97 g/mol
Formula C₈H₉BO₃
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, often in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of advanced materials, such as polymers and sensors, due to its ability to interact with diols and other functional groups. Its formyl group further allows for derivatization, making it versatile in designing target-specific compounds.

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Test Parameter Specification
Appearance Solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,460.00
inventory 1g
10-20 days ฿8,460.00

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(3-Formyl-5-methylphenyl)boronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, often in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of advanced materials, such as polymers and sensors, due to its ability to interact with di

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, often in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of advanced materials, such as polymers and sensors, due to its ability to interact with diols and other functional groups. Its formyl group further allows for derivatization, making it versatile in designing target-specific compounds.

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