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Structure of 1612792-88-7
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This potassium (rel-(1R,2R)-2-(ethoxycarbonyl)cyclopropyl)trifluoroborate delivers a chiral cyclopropyl trifluoroborate unit with high stereochemical integrity. The rel-(1R,2R) configuration ensures predictable reactivity in transition-metal-catalyzed cross-coupling processes. Bench-stable and moisture-tolerant, it integrates seamlessly into synthetic workflows requiring stereoselective carbon–carbon bond formation.
Potassium (rel-(1R,2R)-2-(ethoxycarbonyl)cyclopropyl)trifluoroborate serves as a stable, bench-ready building block for the stereoselective construction of cyclopropyl-containing scaffolds. Its trifluoroborate group enables efficient Suzuki-Miyaura cross-coupling under mild conditions, facilitating C–C bond formation with broad functional group tolerance. The rigid cyclopropyl framework imparts conformational constraint, making it valuable in medicinal chemistry and catalytic synthesis.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: