Potassium (E)-but-2-en-1-yltrifluoroborate

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Reagent Code: #181090
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CAS Number 233666-81-4

science Other reagents with same CAS 233666-81-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 162 g/mol
Formula C₄H₇BF₃K
badge Registry Numbers
MDL Number MFCD30189220
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its trifluoroborate group provides stability and controlled reactivity, making it suitable for constructing complex molecules in pharmaceutical and agrochemical research. The (E)-but-2-en-1-yl moiety allows for the introduction of an alkenyl chain with defined stereochemistry, useful in the synthesis of bioactive compounds. Soluble in aqueous and organic solvent mixtures, it supports mild reaction conditions and broad functional group tolerance.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,250.00
inventory 250mg
10-20 days ฿22,500.00

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Potassium (E)-but-2-en-1-yltrifluoroborate
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Used as a reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its trifluoroborate group provides stability and controlled reactivity, making it suitable for constructing complex molecules in pharmaceutical and agrochemical research. The (E)-but-2-en-1-yl moiety allows for the introduction of an alkenyl chain with defined stereochemistry, useful in the synthesis of bioactive compounds. Soluble in aqueous and organic solvent mixtures, it supp
Used as a reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its trifluoroborate group provides stability and controlled reactivity, making it suitable for constructing complex molecules in pharmaceutical and agrochemical research. The (E)-but-2-en-1-yl moiety allows for the introduction of an alkenyl chain with defined stereochemistry, useful in the synthesis of bioactive compounds. Soluble in aqueous and organic solvent mixtures, it supports mild reaction conditions and broad functional group tolerance.
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