Potassium 3-carboxyphenyltrifluoroborate

98%

Reagent Code: #226137
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CAS Number 850313-91-6

science Other reagents with same CAS 850313-91-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.0179 g/mol
Formula C₇H₅BF₃KO₂
badge Registry Numbers
MDL Number MFCD07784423
thermostat Physical Properties
Melting Point >300℃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a coupling reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its trifluoroborate group provides enhanced stability and controlled reactivity with aryl halides under palladium catalysis. The carboxylic acid functionality allows for further derivatization or conjugation, making it valuable in the preparation of biaryl compounds, drug intermediates, and functional materials. Soluble in aqueous and organic solvent systems, it supports green chemistry approaches by facilitating reactions in mixed or aqueous media.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,122.00
inventory 5g
10-20 days ฿3,751.00
inventory 25g
10-20 days ฿18,430.50
Potassium 3-carboxyphenyltrifluoroborate
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Used as a coupling reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its trifluoroborate group provides enhanced stability and controlled reactivity with aryl halides under palladium catalysis. The carboxylic acid functionality allows for further derivatization or conjugation, making it valuable in the preparation of biaryl compounds, drug intermediates, and functional materials. Soluble in aqueous and organic s

Used as a coupling reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its trifluoroborate group provides enhanced stability and controlled reactivity with aryl halides under palladium catalysis. The carboxylic acid functionality allows for further derivatization or conjugation, making it valuable in the preparation of biaryl compounds, drug intermediates, and functional materials. Soluble in aqueous and organic solvent systems, it supports green chemistry approaches by facilitating reactions in mixed or aqueous media.

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