4,4,5,5-Tetramethyl-2-(2,4,6-trifluorophenyl)-1,3,2-dioxaborolane

98%

Reagent Code: #241560
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CAS Number 325143-04-2

science Other reagents with same CAS 325143-04-2

blur_circular Chemical Specifications

thermostat Physical Properties
Boiling Point 269.0±40.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.17±0.1g/ml(Predicted)
Storage 2-8℃, dry, sealed

description Product Description

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its electron-deficient aryl group enhances reactivity and stability, making it particularly effective in coupling with aryl and heteroaryl halides under mild conditions. Commonly employed in pharmaceutical and agrochemical research for constructing biaryl scaffolds. Also utilized in materials science for preparing conjugated polymers and organic electronic materials due to its reliable performance in palladium-catalyzed transformations.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿850.00
5g
10-20 days ฿3,780.00
25g
10-20 days ฿16,800.00
4,4,5,5-Tetramethyl-2-(2,4,6-trifluorophenyl)-1,3,2-dioxaborolane
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Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its electron-deficient aryl group enhances reactivity and stability, making it particularly effective in coupling with aryl and heteroaryl halides under mild conditions. Commonly employed in pharmaceutical and agrochemical research for constructing biaryl scaffolds. Also utilized in materials science for preparing conjugated polymers and organic el

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its electron-deficient aryl group enhances reactivity and stability, making it particularly effective in coupling with aryl and heteroaryl halides under mild conditions. Commonly employed in pharmaceutical and agrochemical research for constructing biaryl scaffolds. Also utilized in materials science for preparing conjugated polymers and organic electronic materials due to its reliable performance in palladium-catalyzed transformations.

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