Potassium allyltrifluoroborate,99%

95%

Reagent Code: #78949
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CAS Number 233664-53-4

science Other reagents with same CAS 233664-53-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 147.97 g/mol
Formula C₃H₅BF₃K
badge Registry Numbers
MDL Number MFCD07368222
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Potassium allyltrifluoroborate is widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura coupling. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a stable and efficient allylating agent, enabling the introduction of allyl groups into complex molecules. Its high reactivity and compatibility with various catalysts make it a preferred choice in medicinal chemistry for synthesizing biologically active compounds. Additionally, it is utilized in the development of polymers and fine chemicals, where precise control over molecular structure is required.

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Test Parameter Specification
Appearance White - almost white crystal - powder
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿4,250.00
inventory 250mg
10-20 days ฿450.00
inventory 5g
10-20 days ฿1,650.00
inventory 1g
10-20 days ฿750.00

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Potassium allyltrifluoroborate,99%
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Potassium allyltrifluoroborate is widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura coupling. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a stable and efficient allylating agent, enabling the introduction of allyl groups into complex molecules. Its high reactivity and compatibility with various catalysts make it a prefer

Potassium allyltrifluoroborate is widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura coupling. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a stable and efficient allylating agent, enabling the introduction of allyl groups into complex molecules. Its high reactivity and compatibility with various catalysts make it a preferred choice in medicinal chemistry for synthesizing biologically active compounds. Additionally, it is utilized in the development of polymers and fine chemicals, where precise control over molecular structure is required.

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