Potassium ((diethylamino)methyl)trifluoroborate

95%

Reagent Code: #227281
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CAS Number 936329-95-2

science Other reagents with same CAS 936329-95-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.06 g/mol
Formula C₅H₁₂BF₃KN
badge Registry Numbers
MDL Number MFCD11052700
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it serves as a stable and easy-to-handle source of nucleophilic ((diethylamino)methyl) species. Its boron-based structure allows for efficient carbon-carbon bond formation under mild conditions, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and functional materials. The reagent’s stability and solubility profile enhance reaction reproducibility and reduce the need for stringent handling conditions compared to more sensitive organometallic reagents.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,330.00
250mg
10-20 days ฿2,250.00
1g
10-20 days ฿6,100.00
Potassium ((diethylamino)methyl)trifluoroborate
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Used as a reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it serves as a stable and easy-to-handle source of nucleophilic ((diethylamino)methyl) species. Its boron-based structure allows for efficient carbon-carbon bond formation under mild conditions, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and functional materials. The reagent’s stability and solubility profile enhance reaction reproducibility and reduce the need
Used as a reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it serves as a stable and easy-to-handle source of nucleophilic ((diethylamino)methyl) species. Its boron-based structure allows for efficient carbon-carbon bond formation under mild conditions, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and functional materials. The reagent’s stability and solubility profile enhance reaction reproducibility and reduce the need for stringent handling conditions compared to more sensitive organometallic reagents.
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