Potassium trifluoro(pent-4-en-1-yl)borate

95%

Reagent Code: #227807
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CAS Number 882871-23-0

science Other reagents with same CAS 882871-23-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.03 g/mol
Formula C₅H₉BF₃K
badge Registry Numbers
MDL Number MFCD20291906
inventory_2 Storage & Handling
Storage -20°C, Sealed, Drying, 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 boron-based nucleophile. Its terminal alkene functionality allows for further chemical modifications, including hydrofunctionalization or polymerization reactions. This makes it valuable in the preparation of complex organic molecules, especially in pharmaceutical and agrochemical industries where tailored carbon frameworks are required. The trifluoro borate group enhances stability and reactivity control, improving selectivity in bond-forming reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿4,800.00
1g
10-20 days ฿12,600.00
5g
10-20 days ฿54,870.00
Potassium trifluoro(pent-4-en-1-yl)borate
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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 boron-based nucleophile. Its terminal alkene functionality allows for further chemical modifications, including hydrofunctionalization or polymerization reactions. This makes it valuable in the preparation of complex organic molecules, especially in pharmaceutical and agrochemical industries where tailored carbon frameworks are required. The trifluoro borate group enhance

Used as a reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it serves as a boron-based nucleophile. Its terminal alkene functionality allows for further chemical modifications, including hydrofunctionalization or polymerization reactions. This makes it valuable in the preparation of complex organic molecules, especially in pharmaceutical and agrochemical industries where tailored carbon frameworks are required. The trifluoro borate group enhances stability and reactivity control, improving selectivity in bond-forming reactions.

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