(5aS,10bR)-2-Mesityl-9-nitro-5a,10b-dihydro-4H,6H-indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazin-2-ium tetrafluoroborate

97%

Reagent Code: #233675
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CAS Number 1827720-62-6

science Other reagents with same CAS 1827720-62-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 464.22 g/mol
Formula C₂₁H₂₁BF₄N₄O₃
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used in organic synthesis as a chiral catalyst or intermediate in asymmetric reactions, particularly in the development of enantioselective transformations. Its rigid polycyclic structure and defined stereochemistry make it suitable for promoting stereoselectivity in carbon–carbon bond-forming reactions. Often employed in academic and pharmaceutical research for constructing complex molecules with high optical purity. The mesityl and nitro groups contribute to steric bulk and electronic tuning, enhancing selectivity in catalytic processes. Also explored in materials science for designing novel ionic architectures with potential optoelectronic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿25,180.00
inventory 250mg
10-20 days ฿50,240.00
inventory 1g
10-20 days ฿140,660.00

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(5aS,10bR)-2-Mesityl-9-nitro-5a,10b-dihydro-4H,6H-indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazin-2-ium tetrafluoroborate
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Used in organic synthesis as a chiral catalyst or intermediate in asymmetric reactions, particularly in the development of enantioselective transformations. Its rigid polycyclic structure and defined stereochemistry make it suitable for promoting stereoselectivity in carbon–carbon bond-forming reactions. Often employed in academic and pharmaceutical research for constructing complex molecules with high optical purity. The mesityl and nitro groups contribute to steric bulk and electronic tuning, enhancing

Used in organic synthesis as a chiral catalyst or intermediate in asymmetric reactions, particularly in the development of enantioselective transformations. Its rigid polycyclic structure and defined stereochemistry make it suitable for promoting stereoselectivity in carbon–carbon bond-forming reactions. Often employed in academic and pharmaceutical research for constructing complex molecules with high optical purity. The mesityl and nitro groups contribute to steric bulk and electronic tuning, enhancing selectivity in catalytic processes. Also explored in materials science for designing novel ionic architectures with potential optoelectronic properties.

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