Potassium ((cyclopentyloxy)methyl)trifluoroborate

98%

Reagent Code: #227124
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CAS Number 1027642-31-4

science Other reagents with same CAS 1027642-31-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.05 g/mol
Formula C₆H₁₁BF₃KO
badge Registry Numbers
MDL Number MFCD11505926
inventory_2 Storage & Handling
Storage -20°C, Inert Gas

description Product Description

Used as a boron reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its stability and reactivity make it suitable for constructing complex molecules, especially in pharmaceutical and agrochemical industries. The trifluoroborate group offers enhanced shelf life and reduced toxicity compared to other boronic derivatives, allowing safer handling and improved reaction selectivity. Commonly employed in late-stage functionalization of aromatic systems where mild reaction conditions are required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿730.00
inventory 1g
10-20 days ฿2,280.00
inventory 5g
10-20 days ฿10,630.00
Potassium ((cyclopentyloxy)methyl)trifluoroborate
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Used as a boron reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its stability and reactivity make it suitable for constructing complex molecules, especially in pharmaceutical and agrochemical industries. The trifluoroborate group offers enhanced shelf life and reduced toxicity compared to other boronic derivatives, allowing safer handling and improved reaction selectivity. Commonly employed in late-stage functionalization of aromatic

Used as a boron reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its stability and reactivity make it suitable for constructing complex molecules, especially in pharmaceutical and agrochemical industries. The trifluoroborate group offers enhanced shelf life and reduced toxicity compared to other boronic derivatives, allowing safer handling and improved reaction selectivity. Commonly employed in late-stage functionalization of aromatic systems where mild reaction conditions are required.

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