2-(2-Ethoxy-5-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95%

Reagent Code: #131121
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CAS Number 1268511-93-8

science Other reagents with same CAS 1268511-93-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.12 g/mol
Formula C₁₅H₂₀BF₃O₃
thermostat Physical Properties
Boiling Point 360.1±42.0 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable for constructing complex aromatic systems. Commonly employed in late-stage functionalization of bioactive molecules due to its stability and reactivity profile. Also utilized in materials science for synthesizing conjugated organic frameworks and functionalized polymers.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,330.00
inventory 5g
10-20 days ฿4,920.00

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2-(2-Ethoxy-5-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable for constructing complex aromatic systems. Commonly employed in late-stage functionalization of bioactive molecules due to its stability and reactivity profile. Also utilized in materials science for synthesizing conjugated organic frameworks and

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable for constructing complex aromatic systems. Commonly employed in late-stage functionalization of bioactive molecules due to its stability and reactivity profile. Also utilized in materials science for synthesizing conjugated organic frameworks and functionalized polymers.

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