(2-Ethoxy-4-(trifluoromethyl)phenyl)boronic acid

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Reagent Code: #184989
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CAS Number 1260518-74-8

science Other reagents with same CAS 1260518-74-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.98 g/mol
Formula C₉H₁₀BF₃O₃
badge Registry Numbers
MDL Number MFCD18087684
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. Its boronic acid functionality enables the formation of carbon-carbon bonds, making it valuable in creating biaryl compounds with specific electronic and steric properties. The presence of ethoxy and trifluoromethyl groups enhances substrate reactivity and influences the biological activity of target molecules, especially in drug discovery programs aiming for improved metabolic stability and binding affinity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,840.00
inventory 250mg
10-20 days ฿4,820.00
inventory 1g
10-20 days ฿13,000.00

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(2-Ethoxy-4-(trifluoromethyl)phenyl)boronic acid
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. Its boronic acid functionality enables the formation of carbon-carbon bonds, making it valuable in creating biaryl compounds with specific electronic and steric properties. The presence of ethoxy and trifluoromethyl groups enhances substrate reactivity and influences the biological activity of target molecules, especially in drug

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. Its boronic acid functionality enables the formation of carbon-carbon bonds, making it valuable in creating biaryl compounds with specific electronic and steric properties. The presence of ethoxy and trifluoromethyl groups enhances substrate reactivity and influences the biological activity of target molecules, especially in drug discovery programs aiming for improved metabolic stability and binding affinity.

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