Potassium2,6-dimethoxy-3-pyridinetrifluoroborate

98%

Reagent Code: #227905
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CAS Number 1374247-42-3

science Other reagents with same CAS 1374247-42-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.05 g/mol
Formula C₇H₈BF₃KNO₂
badge Registry Numbers
MDL Number MFCD22124437
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used as a 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 complex pyridine-containing molecules, often found in bioactive compounds and functional materials. The trifluoroborate group enhances shelf life and handling compared to boronic acids, while still generating active catalytic species under mild conditions. Commonly applied in late-stage functionalization where sensitive functional groups are present.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿4,240.00
1g
10-20 days ฿12,000.00
5g
10-20 days ฿55,990.00
Potassium2,6-dimethoxy-3-pyridinetrifluoroborate
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Used as a 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 complex pyridine-containing molecules, often found in bioactive compounds and functional materials. The trifluoroborate group enhances shelf life and handling compared to boronic acids, while still generating active catalytic species under mild conditions. Commonly applied in late-stage func

Used as a 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 complex pyridine-containing molecules, often found in bioactive compounds and functional materials. The trifluoroborate group enhances shelf life and handling compared to boronic acids, while still generating active catalytic species under mild conditions. Commonly applied in late-stage functionalization where sensitive functional groups are present.

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