(3-benzyloxy-2-chloro-6-fluoro-phenyl)boronic acid

98%

Reagent Code: #90280
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CAS Number 957062-67-8

science Other reagents with same CAS 957062-67-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.487 g/mol
Formula C₁₃H₁₁BClFO₃
badge Registry Numbers
MDL Number MFCD09878328
thermostat Physical Properties
Boiling Point 461.183℃ at 760 mmHg
inventory_2 Storage & Handling
Storage Dry, sealed, 2-8℃

description Product Description

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules. Its boronic acid group is highly reactive with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical research and the development of active pharmaceutical ingredients (APIs). Additionally, it is utilized in the production of advanced materials, such as polymers and liquid crystals, due to its ability to introduce specific functional groups into molecular structures. Its fluorine and chlorine substituents enhance its reactivity and selectivity in various chemical transformations.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,205.00
inventory 5g
10-20 days ฿6,561.00

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(3-benzyloxy-2-chloro-6-fluoro-phenyl)boronic acid
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This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules. Its boronic acid group is highly reactive with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical research and the development of active pharmaceutical ingredients (APIs). Additionally, it is utilized in the production of

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules. Its boronic acid group is highly reactive with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical research and the development of active pharmaceutical ingredients (APIs). Additionally, it is utilized in the production of advanced materials, such as polymers and liquid crystals, due to its ability to introduce specific functional groups into molecular structures. Its fluorine and chlorine substituents enhance its reactivity and selectivity in various chemical transformations.

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