Potassium (2,2-difluorocyclopropyl)trifluoroborate

98%

Reagent Code: #227562
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CAS Number 2416056-30-7

science Other reagents with same CAS 2416056-30-7

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its stability and reactivity make it valuable for constructing fluorinated organic compounds, which are important in pharmaceutical and agrochemical development due to their enhanced metabolic stability and bioavailability. The difluorocyclopropyl group can serve as a bioisostere, improving the pharmacokinetic properties of drug candidates. It is also employed in the synthesis of complex molecules where selective coupling and functional group tolerance are required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿5,620.00
250mg
10-20 days ฿7,510.00
1g
10-20 days ฿20,340.00
Potassium (2,2-difluorocyclopropyl)trifluoroborate
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Used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its stability and reactivity make it valuable for constructing fluorinated organic compounds, which are important in pharmaceutical and agrochemical development due to their enhanced metabolic stability and bioavailability. The difluorocyclopropyl group can serve as a bioisostere, improving the pharmacokinetic properties of drug candidates. It is also employed in

Used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its stability and reactivity make it valuable for constructing fluorinated organic compounds, which are important in pharmaceutical and agrochemical development due to their enhanced metabolic stability and bioavailability. The difluorocyclopropyl group can serve as a bioisostere, improving the pharmacokinetic properties of drug candidates. It is also employed in the synthesis of complex molecules where selective coupling and functional group tolerance are required.

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