Potassium (2,6-dimethylphenyl)trifluoroborate

98%

Reagent Code: #226162
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CAS Number 561328-67-4

science Other reagents with same CAS 561328-67-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.06 g/mol
Formula C₈H₉BF₃K
badge Registry Numbers
MDL Number MFCD04974103
thermostat Physical Properties
Melting Point 298℃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a coupling reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of pharmaceuticals and agrochemicals. Its stability and reactivity make it suitable for constructing biaryl compounds under mild conditions. Commonly employed in late-stage functionalization of complex molecules where traditional boronic acids may degrade or react nonspecifically. Also applied in medicinal chemistry for the development of kinase inhibitors and other bioactive molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿900.00
inventory 1g
10-20 days ฿2,380.00
inventory 5g
10-20 days ฿8,580.00
Potassium (2,6-dimethylphenyl)trifluoroborate
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Used as a coupling reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of pharmaceuticals and agrochemicals. Its stability and reactivity make it suitable for constructing biaryl compounds under mild conditions. Commonly employed in late-stage functionalization of complex molecules where traditional boronic acids may degrade or react nonspecifically. Also applied in medicinal chemistry for the development of kinase inhibitors and other bioact

Used as a coupling reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of pharmaceuticals and agrochemicals. Its stability and reactivity make it suitable for constructing biaryl compounds under mild conditions. Commonly employed in late-stage functionalization of complex molecules where traditional boronic acids may degrade or react nonspecifically. Also applied in medicinal chemistry for the development of kinase inhibitors and other bioactive molecules.

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