Urea, N-(4-methyl-2-pyridinyl)-N'-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-

95%

Reagent Code: #245104
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CAS Number 1800110-44-4

science Other reagents with same CAS 1800110-44-4

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Weight 353.22316 g/mol
Formula C₁₉H₂₄BN₃O₃
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the synthesis of complex biaryl structures found in pharmaceuticals and agrochemicals. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in drug discovery and development of organic electronic materials. The urea linkage adds polarity and hydrogen-bonding capability, which can enhance binding selectivity in bioactive molecules. It is particularly useful in constructing kinase inhibitors and other targeted therapies in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿22,400.00
inventory 1g
10-20 days ฿48,000.00

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Urea, N-(4-methyl-2-pyridinyl)-N'-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the synthesis of complex biaryl structures found in pharmaceuticals and agrochemicals. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in drug discovery and development of organic electronic materials. The urea linkage adds polarity and hydrogen-bonding capability, which can enhance binding selectivity in bioactive molecules. It is particularly useful in con

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the synthesis of complex biaryl structures found in pharmaceuticals and agrochemicals. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in drug discovery and development of organic electronic materials. The urea linkage adds polarity and hydrogen-bonding capability, which can enhance binding selectivity in bioactive molecules. It is particularly useful in constructing kinase inhibitors and other targeted therapies in medicinal chemistry research.

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