4,4,5,5-Tetramethyl-2-(5-nitro-2-(trifluoromethoxy)phenyl)-1,3,2-dioxaborolane

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Reagent Code: #131696
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CAS Number 2236064-16-5

science Other reagents with same CAS 2236064-16-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 333.07 g/mol
Formula C₁₃H₁₅BF₃NO₅
thermostat Physical Properties
Boiling Point 376.5±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.30±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

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. Particularly valuable in pharmaceutical and agrochemical industries for constructing biaryl systems where one partner contains electron-withdrawing or fluorinated substituents. The presence of the nitro and trifluoromethoxy groups enhances reactivity and influences regioselectivity in coupling processes. Its stability and reactivity profile make it suitable for late-stage functionalization in drug discovery and development of functional materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,100.00
inventory 250mg
10-20 days ฿3,560.00
inventory 1g
10-20 days ฿9,600.00

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4,4,5,5-Tetramethyl-2-(5-nitro-2-(trifluoromethoxy)phenyl)-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. Particularly valuable in pharmaceutical and agrochemical industries for constructing biaryl systems where one partner contains electron-withdrawing or fluorinated substituents. The presence of the nitro and trifluoromethoxy groups enhances reactivity and influences regioselectivity in coupling processes. Its stability and reactivity profile ma

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. Particularly valuable in pharmaceutical and agrochemical industries for constructing biaryl systems where one partner contains electron-withdrawing or fluorinated substituents. The presence of the nitro and trifluoromethoxy groups enhances reactivity and influences regioselectivity in coupling processes. Its stability and reactivity profile make it suitable for late-stage functionalization in drug discovery and development of functional materials.

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