POTASSIUM CIS-(2-(ETHOXYCARBONYL)CYCLOPROPYL)TRIFLUOROBORATE

95%

Reagent Code: #223304
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CAS Number 1613220-84-0

science Other reagents with same CAS 1613220-84-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.039 g/mol
Formula C₆H₉BF₃KO₂
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MDL Number MFCD31617827
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its cyclopropane structure with a trifluoroborate group provides enhanced stability and reactivity, making it valuable for constructing complex molecules in pharmaceutical and agrochemical development. The ethoxycarbonyl group allows further functionalization, supporting versatile downstream modifications. Commonly applied in the synthesis of bioactive compounds where strained ring systems improve metabolic stability and binding affinity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿16,000.00
250mg
10-20 days ฿32,000.00
500mg
10-20 days ฿56,000.00
1g
10-20 days ฿96,000.00
POTASSIUM CIS-(2-(ETHOXYCARBONYL)CYCLOPROPYL)TRIFLUOROBORATE
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Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its cyclopropane structure with a trifluoroborate group provides enhanced stability and reactivity, making it valuable for constructing complex molecules in pharmaceutical and agrochemical development. The ethoxycarbonyl group allows further functionalization, supporting versatile downstream modifications. Commonly applied in the synthesis of bioactive compounds where stra

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its cyclopropane structure with a trifluoroborate group provides enhanced stability and reactivity, making it valuable for constructing complex molecules in pharmaceutical and agrochemical development. The ethoxycarbonyl group allows further functionalization, supporting versatile downstream modifications. Commonly applied in the synthesis of bioactive compounds where strained ring systems improve metabolic stability and binding affinity.

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