4-Butylphenylboronic acid pinacol ester

98%

Reagent Code: #148040
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CAS Number 625458-85-7

science Other reagents with same CAS 625458-85-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.1900 g/mol
Formula C₁₆H₂₅BO₂
badge Registry Numbers
MDL Number MFCD20527105
thermostat Physical Properties
Boiling Point 345.2±21.0℃(Predicted)
inventory_2 Storage & Handling
Density 0.96±0.1g/ml(Predicted)
Storage 2-8℃, dry, sealed

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronic ester group offers enhanced stability and handling compared to the corresponding boronic acid, making it suitable for large-scale applications. Commonly employed in the preparation of liquid crystals, organic semiconductors, and bioactive molecules where precise aryl-aryl coupling is required. The pinacol protecting group facilitates purification and storage, while being readily cleaved under mild conditions when needed.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,970.00
inventory 1g
10-20 days ฿5,520.00
inventory 5g
10-20 days ฿20,690.00

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4-Butylphenylboronic acid pinacol ester
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronic ester group offers enhanced stability and handling compared to the corresponding boronic acid, making it suitable for large-scale applications. Commonly employed in the preparation of liquid crystals, organic semiconductors, and bioactive molecules where precise aryl-aryl coupling is required. The pinacol protecting group facilitate

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronic ester group offers enhanced stability and handling compared to the corresponding boronic acid, making it suitable for large-scale applications. Commonly employed in the preparation of liquid crystals, organic semiconductors, and bioactive molecules where precise aryl-aryl coupling is required. The pinacol protecting group facilitates purification and storage, while being readily cleaved under mild conditions when needed.

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