Potassium trifluoro(4-methylbenzyl)borate

95%

Reagent Code: #227276
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CAS Number 1422539-95-4

science Other reagents with same CAS 1422539-95-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.06 g/mol
Formula C₈H₉BF₃K
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MDL Number MFCD09993057
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions for the efficient introduction of the 4-methylbenzyl group to aryl or heteroaryl halides. It acts as a stable nucleophilic boron species, enabling selective C-C bond formation under mild conditions. This is valuable in pharmaceutical and agrochemical industries for building complex molecular architectures, enhancing properties like metabolic stability and bioavailability. Its air and moisture stability, along with good solubility, makes it compatible with a wide range of functional groups and reduces side reactions. Commonly applied in the development of drug candidates, bioactive molecules, and advanced materials.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,430.00
250mg
10-20 days ฿3,330.00
1g
10-20 days ฿10,930.00
Potassium trifluoro(4-methylbenzyl)borate
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Used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions for the efficient introduction of the 4-methylbenzyl group to aryl or heteroaryl halides. It acts as a stable nucleophilic boron species, enabling selective C-C bond formation under mild conditions. This is valuable in pharmaceutical and agrochemical industries for building complex molecular architectures, enhancing properties like metabolic stability and bioavailability. Its air and moisture stability, along

Used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions for the efficient introduction of the 4-methylbenzyl group to aryl or heteroaryl halides. It acts as a stable nucleophilic boron species, enabling selective C-C bond formation under mild conditions. This is valuable in pharmaceutical and agrochemical industries for building complex molecular architectures, enhancing properties like metabolic stability and bioavailability. Its air and moisture stability, along with good solubility, makes it compatible with a wide range of functional groups and reduces side reactions. Commonly applied in the development of drug candidates, bioactive molecules, and advanced materials.

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