3-Chloro-4-methoxyphenylboronic acid pinacol ester

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Reagent Code: #161737
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CAS Number 1165936-01-5

science Other reagents with same CAS 1165936-01-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.5595 g/mol
Formula C₁₃H₂₀BClO₄
thermostat Physical Properties
Boiling Point 352.7±32.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.12±0.1g/ml(Predicted)
Storage 2-8℃, dry, sealed

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic ester group provides enhanced stability and handling compared to the corresponding boronic acid, making it a preferred reagent in palladium-catalyzed coupling processes. Commonly employed in the construction of biaryl systems and functionalized aromatic compounds for drug discovery and materials science.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,340.00
inventory 5g
10-20 days ฿20,200.00
inventory 1g
10-20 days ฿6,880.00

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3-Chloro-4-methoxyphenylboronic acid pinacol ester
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Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic ester group provides enhanced stability and handling compared to the corresponding boronic acid, making it a preferred reagent in palladium-catalyzed coupling processes. Commonly employed in the construction of biaryl systems and functionalized aromatic compounds for drug discovery and materials science.

Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic ester group provides enhanced stability and handling compared to the corresponding boronic acid, making it a preferred reagent in palladium-catalyzed coupling processes. Commonly employed in the construction of biaryl systems and functionalized aromatic compounds for drug discovery and materials science.

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