2-(3,5-Dichlorophenyl)-4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane

≥98%

Reagent Code: #89934
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CAS Number 68716-51-8

science Other reagents with same CAS 68716-51-8

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Weight 272.96 g/mol
Formula C₁₂H₁₅BCl₂O₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized as a key intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It plays a crucial role in the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronate ester structure makes it highly reactive and suitable for coupling with aryl halides, facilitating the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of organic electronic materials, where precise molecular architecture is essential. Its stability and reactivity under mild conditions make it a valuable tool in modern synthetic chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿315.00
inventory 5g
10-20 days ฿1,530.00
inventory 25g
10-20 days ฿7,110.00

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2-(3,5-Dichlorophenyl)-4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane
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This chemical is primarily utilized as a key intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It plays a crucial role in the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronate ester structure makes it highly reactive and suitable for coupling with aryl halides, facilitating the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development o

This chemical is primarily utilized as a key intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It plays a crucial role in the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronate ester structure makes it highly reactive and suitable for coupling with aryl halides, facilitating the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of organic electronic materials, where precise molecular architecture is essential. Its stability and reactivity under mild conditions make it a valuable tool in modern synthetic chemistry.

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