(R)-5-isopropyl-2-(perfluorophenyl)-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-2-ium tetrafluoroborate

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Reagent Code: #231231
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CAS Number 1175052-07-9

science Other reagents with same CAS 1175052-07-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 405.07 g/mol
Formula C₁₄H₁₃BF₉N₃
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral organocatalyst in asymmetric synthesis, particularly in enantioselective fluorination and trifluoromethylation reactions. Its unique perfluorophenyl and isopropyl substituents enhance both reactivity and stereocontrol, making it effective for constructing chiral centers in pharmaceutical intermediates. The tetrafluoroborate counterion contributes to solubility in polar aprotic solvents, facilitating its use in homogeneous catalytic systems. Commonly applied in the development of bioactive molecules where high enantiomeric excess is required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,190.00
inventory 1g
10-20 days ฿31,760.00
inventory 250mg
10-20 days ฿9,650.00

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(R)-5-isopropyl-2-(perfluorophenyl)-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-2-ium tetrafluoroborate
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Used as a chiral organocatalyst in asymmetric synthesis, particularly in enantioselective fluorination and trifluoromethylation reactions. Its unique perfluorophenyl and isopropyl substituents enhance both reactivity and stereocontrol, making it effective for constructing chiral centers in pharmaceutical intermediates. The tetrafluoroborate counterion contributes to solubility in polar aprotic solvents, facilitating its use in homogeneous catalytic systems. Commonly applied in the development of bioactiv

Used as a chiral organocatalyst in asymmetric synthesis, particularly in enantioselective fluorination and trifluoromethylation reactions. Its unique perfluorophenyl and isopropyl substituents enhance both reactivity and stereocontrol, making it effective for constructing chiral centers in pharmaceutical intermediates. The tetrafluoroborate counterion contributes to solubility in polar aprotic solvents, facilitating its use in homogeneous catalytic systems. Commonly applied in the development of bioactive molecules where high enantiomeric excess is required.

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