2-(2,5-Dichlorofuran-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

98%

Reagent Code: #179878
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CAS Number 1618668-22-6

science Other reagents with same CAS 1618668-22-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.93 g/mol
Formula C₁₀H₁₃BCl₂O₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or heteroaryl halides, making it valuable in pharmaceutical and agrochemical research. It is especially useful for introducing the 2,5-dichlorofuran moiety into target structures, which can serve as a building block for bioactive compounds. Its stability and reactivity profile make it suitable for use in late-stage functionalization during drug discovery and development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,330.00
inventory 250mg
10-20 days ฿12,240.00
inventory 1g
10-20 days ฿24,480.00
inventory 5g
10-20 days ฿90,160.00

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2-(2,5-Dichlorofuran-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or heteroaryl halides, making it valuable in pharmaceutical and agrochemical research. It is especially useful for introducing the 2,5-dichlorofuran moiety into target structures, which can serve as a building block for bioactive com

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or heteroaryl halides, making it valuable in pharmaceutical and agrochemical research. It is especially useful for introducing the 2,5-dichlorofuran moiety into target structures, which can serve as a building block for bioactive compounds. Its stability and reactivity profile make it suitable for use in late-stage functionalization during drug discovery and development.

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