potassium (2-(benzyloxy)ethyl)trifluoroborate

95%

Reagent Code: #81890
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CAS Number 1408168-73-9

science Other reagents with same CAS 1408168-73-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.0871 g/mol
Formula C₉H₁₁BF₃KO
badge Registry Numbers
MDL Number MFCD22684708
inventory_2 Storage & Handling
Storage -20°C, sealed, inert gas storage

description Product Description

Used in organic synthesis as a stable and versatile alkyltrifluoroborate reagent for Suzuki-Miyaura cross-coupling reactions. It facilitates the formation of carbon-carbon bonds, particularly for introducing the 2-(benzyloxy)ethyl group into complex molecules like pharmaceuticals and agrochemicals. Its trifluoroborate group enhances stability and reactivity, making it suitable for use in aqueous or mild conditions. Additionally, it is employed in the development of bioactive compounds and materials science research.

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Test Parameter Specification
Appearance White to off-white Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿963.00
inventory 100mg
10-20 days ฿2,412.00

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potassium (2-(benzyloxy)ethyl)trifluoroborate
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Used in organic synthesis as a stable and versatile alkyltrifluoroborate reagent for Suzuki-Miyaura cross-coupling reactions. It facilitates the formation of carbon-carbon bonds, particularly for introducing the 2-(benzyloxy)ethyl group into complex molecules like pharmaceuticals and agrochemicals. Its trifluoroborate group enhances stability and reactivity, making it suitable for use in aqueous or mild conditions. Additionally, it is employed in the development of bioactive compounds and materials scien

Used in organic synthesis as a stable and versatile alkyltrifluoroborate reagent for Suzuki-Miyaura cross-coupling reactions. It facilitates the formation of carbon-carbon bonds, particularly for introducing the 2-(benzyloxy)ethyl group into complex molecules like pharmaceuticals and agrochemicals. Its trifluoroborate group enhances stability and reactivity, making it suitable for use in aqueous or mild conditions. Additionally, it is employed in the development of bioactive compounds and materials science research.

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