(5-Fluoro-3-formyl-2-methoxyphenyl)boronic acid

95%

Reagent Code: #113336
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CAS Number 1072951-73-5

science Other reagents with same CAS 1072951-73-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.96 g/mol
Formula C₈H₈BFO₄
badge Registry Numbers
MDL Number MFCD09265144
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

(5-Fluoro-3-formyl-2-methoxyphenyl)boronic acid is primarily utilized in organic synthesis as a key intermediate for the construction of complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid partner to form carbon-carbon bonds, enabling the synthesis of biaryl compounds. These biaryl structures are essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its unique structure, featuring both formyl and boronic acid functional groups, makes it a versatile building block for designing and synthesizing novel compounds with potential biological activity. Its applications extend to medicinal chemistry, where it is used in the discovery and optimization of drug candidates targeting various diseases.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿9,000.00
inventory 250mg
10-20 days ฿3,339.00
inventory 100mg
10-20 days ฿1,971.00

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(5-Fluoro-3-formyl-2-methoxyphenyl)boronic acid
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(5-Fluoro-3-formyl-2-methoxyphenyl)boronic acid is primarily utilized in organic synthesis as a key intermediate for the construction of complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid partner to form carbon-carbon bonds, enabling the synthesis of biaryl compounds. These biaryl structures are essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its unique structure, featuring both f

(5-Fluoro-3-formyl-2-methoxyphenyl)boronic acid is primarily utilized in organic synthesis as a key intermediate for the construction of complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid partner to form carbon-carbon bonds, enabling the synthesis of biaryl compounds. These biaryl structures are essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its unique structure, featuring both formyl and boronic acid functional groups, makes it a versatile building block for designing and synthesizing novel compounds with potential biological activity. Its applications extend to medicinal chemistry, where it is used in the discovery and optimization of drug candidates targeting various diseases.

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