Potassium (3-(ethoxycarbonyl)phenyl)trifluoroborate

98%

Reagent Code: #226178
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CAS Number 1412414-43-7

science Other reagents with same CAS 1412414-43-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256 g/mol
Formula C₉H₉BF₃KO₂
badge Registry Numbers
MDL Number MFCD28964114
inventory_2 Storage & Handling
Storage 2-8℃, sealed, dried

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 stability and reactivity make it suitable for constructing biaryl compounds, which are common structural motifs in drug development. The ethoxycarbonyl group allows for further functionalization, enhancing versatility in multi-step organic syntheses. Commonly employed in mild reaction conditions, it supports high yields with reduced byproduct formation.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿8,220.00
5g
10-20 days ฿19,600.00
Potassium (3-(ethoxycarbonyl)phenyl)trifluoroborate
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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 stability and reactivity make it suitable for constructing biaryl compounds, which are common structural motifs in drug development. The ethoxycarbonyl group allows for further functionalization, enhancing versatility in multi-step organic syntheses. Commonly employed in mild reaction conditions, it supports high yields with reduced byprodu

Used as a coupling reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its stability and reactivity make it suitable for constructing biaryl compounds, which are common structural motifs in drug development. The ethoxycarbonyl group allows for further functionalization, enhancing versatility in multi-step organic syntheses. Commonly employed in mild reaction conditions, it supports high yields with reduced byproduct formation.

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