3-Ethoxy-2-fluorobenzeneboronic Acid (contains varying amounts of Anhydride)

98%

Reagent Code: #183070
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CAS Number 855230-61-4

science Other reagents with same CAS 855230-61-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183.97 g/mol
Formula C₈H₁₀BFO₃
badge Registry Numbers
MDL Number MFCD06798077
thermostat Physical Properties
Melting Point 78-83°C(lit.)
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions, to construct carbon-carbon bonds. Its boronic acid functionality allows it to react with aryl or vinyl halides in the presence of a palladium catalyst, enabling the formation of substituted aromatic compounds. The presence of both fluoro and ethoxy groups on the aromatic ring influences electronic and steric properties, making it useful for fine-tuning molecular structures in pharmaceuticals, agrochemicals, and advanced materials. The compound’s ability to participate in selective transformations makes it valuable in drug discovery and development of functional molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿400.00
inventory 5g
10-20 days ฿1,580.00
inventory 25g
10-20 days ฿7,210.00
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3-Ethoxy-2-fluorobenzeneboronic Acid (contains varying amounts of Anhydride)
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Used primarily in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions, to construct carbon-carbon bonds. Its boronic acid functionality allows it to react with aryl or vinyl halides in the presence of a palladium catalyst, enabling the formation of substituted aromatic compounds. The presence of both fluoro and ethoxy groups on the aromatic ring influences electronic and steric properties, making it useful for fine-tuning molecular structures in pharmaceuticals, agrochemicals, and ad

Used primarily in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions, to construct carbon-carbon bonds. Its boronic acid functionality allows it to react with aryl or vinyl halides in the presence of a palladium catalyst, enabling the formation of substituted aromatic compounds. The presence of both fluoro and ethoxy groups on the aromatic ring influences electronic and steric properties, making it useful for fine-tuning molecular structures in pharmaceuticals, agrochemicals, and advanced materials. The compound’s ability to participate in selective transformations makes it valuable in drug discovery and development of functional molecules.

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