3-ETHOXYCARBONYL-4-FLUOROPHENYLBORONIC ACID

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Reagent Code: #181854
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Alias 3-ethoxycarbonyl-4-fluorophenylboric acid; 3-ethoxycarbonyl-4-fluorophenylboric acid; 3-ethyl ester-4-fluorophenylboric acid
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CAS Number 874219-36-0

science Other reagents with same CAS 874219-36-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.98 g/mol
Formula C₉H₁₀BFO₄
thermostat Physical Properties
Melting Point 149-152℃
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct carbon-carbon bonds in pharmaceutical intermediates. Its boronic acid group enables coupling with aryl halides, making it valuable in the development of fluorinated aromatic compounds for drug discovery and functional materials. The ester and fluorine substituents enhance reactivity and influence electronic properties, supporting fine-tuning of molecular structures in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿830.00
inventory 5g
10-20 days ฿2,620.00
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3-ETHOXYCARBONYL-4-FLUOROPHENYLBORONIC ACID
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct carbon-carbon bonds in pharmaceutical intermediates. Its boronic acid group enables coupling with aryl halides, making it valuable in the development of fluorinated aromatic compounds for drug discovery and functional materials. The ester and fluorine substituents enhance reactivity and influence electronic properties, supporting fine-tuning of molecular structures in medicinal chemistry.

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to construct carbon-carbon bonds in pharmaceutical intermediates. Its boronic acid group enables coupling with aryl halides, making it valuable in the development of fluorinated aromatic compounds for drug discovery and functional materials. The ester and fluorine substituents enhance reactivity and influence electronic properties, supporting fine-tuning of molecular structures in medicinal chemistry.

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