(R)-5-Benzyl-2-(perfluorophenyl)-5,6-dihydro-8H-[1,2,4]triazolo[3,4-c][1,4]oxazin-2-ium tetrafluoroborate

97%

Reagent Code: #232261
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CAS Number 2758767-35-8

science Other reagents with same CAS 2758767-35-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 469.11 g/mol
Formula C₁₈H₁₃BF₉N₃O
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Used as a chiral organocatalyst in asymmetric synthesis, particularly in enantioselective cyclization and fluorination reactions. Its rigid bicyclic structure and chiral environment enable high stereoselectivity, making it valuable in pharmaceutical research for constructing stereocenters in complex molecules. The perfluorophenyl group enhances catalyst stability and influences electronic properties, improving reactivity in transformations involving electron-deficient substrates. Commonly applied in the development of bioactive compounds where precise stereochemistry is critical.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,620.00
inventory 250mg
10-20 days ฿13,170.00
inventory 1g
10-20 days ฿39,460.00

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(R)-5-Benzyl-2-(perfluorophenyl)-5,6-dihydro-8H-[1,2,4]triazolo[3,4-c][1,4]oxazin-2-ium tetrafluoroborate
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Used as a chiral organocatalyst in asymmetric synthesis, particularly in enantioselective cyclization and fluorination reactions. Its rigid bicyclic structure and chiral environment enable high stereoselectivity, making it valuable in pharmaceutical research for constructing stereocenters in complex molecules. The perfluorophenyl group enhances catalyst stability and influences electronic properties, improving reactivity in transformations involving electron-deficient substrates. Commonly applied in the

Used as a chiral organocatalyst in asymmetric synthesis, particularly in enantioselective cyclization and fluorination reactions. Its rigid bicyclic structure and chiral environment enable high stereoselectivity, making it valuable in pharmaceutical research for constructing stereocenters in complex molecules. The perfluorophenyl group enhances catalyst stability and influences electronic properties, improving reactivity in transformations involving electron-deficient substrates. Commonly applied in the development of bioactive compounds where precise stereochemistry is critical.

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