8-Fluoro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline

95%

Reagent Code: #129894
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CAS Number 2235386-14-6

science Other reagents with same CAS 2235386-14-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 273.11 g/mol
Formula C₁₅H₁₇BFNO₂
badge Registry Numbers
MDL Number MFCD32706315
thermostat Physical Properties
Boiling Point 390.0±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.15±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of fluorinated quinoline derivatives, which are important in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in the development of bioactive molecules and functional materials. Commonly applied in medicinal chemistry for constructing libraries of nitrogen-containing heterocycles with potential antitumor, antimicrobial, or kinase inhibitory activities.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,100.00
inventory 1g
10-20 days ฿5,600.00

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8-Fluoro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of fluorinated quinoline derivatives, which are important in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in the development of bioactive molecules and functional materials. Commonly applied in medicinal chemistry for constructing libraries of nitrogen-containing heterocycles with potential antitumor, antimicrobial, or kinase inhi

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of fluorinated quinoline derivatives, which are important in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in the development of bioactive molecules and functional materials. Commonly applied in medicinal chemistry for constructing libraries of nitrogen-containing heterocycles with potential antitumor, antimicrobial, or kinase inhibitory activities.

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