1H-INDENE-2-BORONIC ACID

Reagent Code: #115005
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CAS Number 312968-21-1

science Other reagents with same CAS 312968-21-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 159.98 g/mol
Formula C₉H₉BO₂
badge Registry Numbers
MDL Number MFCD11506071
thermostat Physical Properties
Melting Point 57-77°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

1H-Indene-2-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the creation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it is employed in the development of sensors and molecular recognition systems due to its ability to interact with diols and other functional groups. Its versatility makes it valuable in research and industrial applications for constructing diverse chemical structures.

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inventory 1g
10-20 days ฿9,000.00

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1H-INDENE-2-BORONIC ACID
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1H-Indene-2-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the creation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it is employed in the development of sensors and mole

1H-Indene-2-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the creation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it is employed in the development of sensors and molecular recognition systems due to its ability to interact with diols and other functional groups. Its versatility makes it valuable in research and industrial applications for constructing diverse chemical structures.

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