Potassium Trifluoro(2-Methylbenzyl)Borate

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Reagent Code: #227683
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CAS Number 1632070-88-2

science Other reagents with same CAS 1632070-88-2

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Weight 211.06 g/mol
Formula C₈H₈BF₃K
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Storage Room temperature

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Potassium trifluoro(2-methylbenzyl)borate is used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a stable source of the 2-methylbenzyl nucleophile, enabling the efficient introduction of this arylalkyl group into pharmaceuticals, agrochemicals, and advanced materials. Its air and water stability allows for cross-coupling reactions under mild conditions, enhancing selectivity and yield in the synthesis of complex fluorinated or non-fluorinated compounds. Commonly applied in medicinal chemistry for developing drug candidates with improved metabolic profiles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,380.00
inventory 250mg
10-20 days ฿20,590.00
inventory 1g
10-20 days ฿58,510.00

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Potassium Trifluoro(2-Methylbenzyl)Borate
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Potassium trifluoro(2-methylbenzyl)borate is used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a stable source of the 2-methylbenzyl nucleophile, enabling the efficient introduction of this arylalkyl group into pharmaceuticals, agrochemicals, and advanced materials. Its air and water stability allows for cross-coupling reactions under mild conditions, enhancing selectivity and yield in the synthesis of complex fluorinated or non-fluorinated comp

Potassium trifluoro(2-methylbenzyl)borate is used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a stable source of the 2-methylbenzyl nucleophile, enabling the efficient introduction of this arylalkyl group into pharmaceuticals, agrochemicals, and advanced materials. Its air and water stability allows for cross-coupling reactions under mild conditions, enhancing selectivity and yield in the synthesis of complex fluorinated or non-fluorinated compounds. Commonly applied in medicinal chemistry for developing drug candidates with improved metabolic profiles.

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