Potassium (benzyloxycarbonylamino)methyltrifluoroborate

97%

Reagent Code: #223287
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CAS Number 1695529-70-4

science Other reagents with same CAS 1695529-70-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.0857 g/mol
Formula C₉H₁₀BF₃KNO₂
badge Registry Numbers
MDL Number MFCD19982304
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. Particularly valuable in peptide chemistry and medicinal chemistry for introducing protected aminoalkyl groups. Its trifluoroborate moiety offers enhanced stability and handling compared to boronic acids, while the benzyloxycarbonyl (Cbz) group provides orthogonal protection for amines during multi-step syntheses. Commonly applied in the preparation of biologically active compounds, including pharmaceuticals and agrochemicals.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,890.00
250mg
10-20 days ฿6,400.00
500mg
10-20 days ฿10,660.00
Potassium (benzyloxycarbonylamino)methyltrifluoroborate
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Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. Particularly valuable in peptide chemistry and medicinal chemistry for introducing protected aminoalkyl groups. Its trifluoroborate moiety offers enhanced stability and handling compared to boronic acids, while the benzyloxycarbonyl (Cbz) group provides orthogonal protection for amines during multi-step syntheses. Commonly applied in the preparation of biologically

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. Particularly valuable in peptide chemistry and medicinal chemistry for introducing protected aminoalkyl groups. Its trifluoroborate moiety offers enhanced stability and handling compared to boronic acids, while the benzyloxycarbonyl (Cbz) group provides orthogonal protection for amines during multi-step syntheses. Commonly applied in the preparation of biologically active compounds, including pharmaceuticals and agrochemicals.

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