2-(3-Chloro-5-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

98%

Reagent Code: #166355
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CAS Number 502630-89-9

science Other reagents with same CAS 502630-89-9

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Weight 252.54 g/mol
Formula C₁₃H₁₈BClO₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Commonly applied in pharmaceutical development and agrochemical research for constructing biaryl structures. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides under mild conditions, making it valuable in medicinal chemistry for building drug-like scaffolds. Also employed in materials science for designing organic semiconductors and functional polymers.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,350.00
inventory 250mg
10-20 days ฿4,090.00
inventory 5g
10-20 days ฿38,500.00
inventory 10g
10-20 days ฿69,300.00
inventory 1g
10-20 days ฿10,870.00

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2-(3-Chloro-5-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Commonly applied in pharmaceutical development and agrochemical research for constructing biaryl structures. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides under mild conditions, making it valuable in medicinal chemistry for building drug-like scaffolds. Also employed in materials science for designing orga

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Commonly applied in pharmaceutical development and agrochemical research for constructing biaryl structures. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides under mild conditions, making it valuable in medicinal chemistry for building drug-like scaffolds. Also employed in materials science for designing organic semiconductors and functional polymers.

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