potassium cyclopentyl(trifluoro)borate(1-)

98%

Reagent Code: #226110
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CAS Number 1040745-70-7

science Other reagents with same CAS 1040745-70-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.0295 g/mol
Formula C₅H₉BF₃K
badge Registry Numbers
MDL Number MFCD04112712
inventory_2 Storage & Handling
Storage -20℃, inert gas

description Product Description

Used as a reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it serves as a source of the cyclopentyl group. Its trifluoroborate structure provides enhanced stability and solubility compared to boronic acids, making it suitable for reactions under aqueous or mild conditions. It enables the formation of carbon-carbon bonds in pharmaceutical and agrochemical intermediates, especially where steric hindrance or functional group tolerance is a concern. The reagent is valued for its ability to introduce cyclopentyl moieties into aromatic or heteroaromatic systems, which are common motifs in bioactive molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,190.00
inventory 10g
10-20 days ฿2,180.00
inventory 25g
10-20 days ฿5,350.00
inventory 100g
10-20 days ฿20,500.00
potassium cyclopentyl(trifluoro)borate(1-)
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Used as a reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it serves as a source of the cyclopentyl group. Its trifluoroborate structure provides enhanced stability and solubility compared to boronic acids, making it suitable for reactions under aqueous or mild conditions. It enables the formation of carbon-carbon bonds in pharmaceutical and agrochemical intermediates, especially where steric hindrance or functional group tolerance is a concern

Used as a reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it serves as a source of the cyclopentyl group. Its trifluoroborate structure provides enhanced stability and solubility compared to boronic acids, making it suitable for reactions under aqueous or mild conditions. It enables the formation of carbon-carbon bonds in pharmaceutical and agrochemical intermediates, especially where steric hindrance or functional group tolerance is a concern. The reagent is valued for its ability to introduce cyclopentyl moieties into aromatic or heteroaromatic systems, which are common motifs in bioactive molecules.

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