N-[(11bS)-4-[[(11bS)-2,6-Bis[3,5-bis(trifluoromethyl)phenyl]-4-[[(trifluoromethyl)sulfonyl]amino]-4λ5-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-ylidene]amino]-2,6-bis[3,5-bis(trifluoromethyl)phenyl]-4λ5-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepi

97%

Reagent Code: #215785
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CAS Number 2016814-98-3

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 1788.1 g/mol
Formula C₇₄H₃₃F₃₀N₃O₈P₂S₂
inventory_2 Storage & Handling
Density 1.65±0.1 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a highly selective chiral catalyst in asymmetric synthesis, particularly in enantioselective transformations such as hydrogenation and C–C bond-forming reactions. Its rigid, sterically hindered structure with multiple trifluoromethyl and sulfonyl groups enhances enantiocontrol and stability under harsh reaction conditions. Commonly applied in pharmaceutical synthesis where high optical purity is required. Also employed in advanced materials research due to its unique phosphorus-based polycyclic framework, contributing to the design of chiral ligands and organocatalysts.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿11,890.00
100mg
10-20 days ฿20,200.00
N-[(11bS)-4-[[(11bS)-2,6-Bis[3,5-bis(trifluoromethyl)phenyl]-4-[[(trifluoromethyl)sulfonyl]amino]-4λ5-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-ylidene]amino]-2,6-bis[3,5-bis(trifluoromethyl)phenyl]-4λ5-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepi
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Used as a highly selective chiral catalyst in asymmetric synthesis, particularly in enantioselective transformations such as hydrogenation and C–C bond-forming reactions. Its rigid, sterically hindered structure with multiple trifluoromethyl and sulfonyl groups enhances enantiocontrol and stability under harsh reaction conditions. Commonly applied in pharmaceutical synthesis where high optical purity is required. Also employed in advanced materials research due to its unique phosphorus-based polycyclic f

Used as a highly selective chiral catalyst in asymmetric synthesis, particularly in enantioselective transformations such as hydrogenation and C–C bond-forming reactions. Its rigid, sterically hindered structure with multiple trifluoromethyl and sulfonyl groups enhances enantiocontrol and stability under harsh reaction conditions. Commonly applied in pharmaceutical synthesis where high optical purity is required. Also employed in advanced materials research due to its unique phosphorus-based polycyclic framework, contributing to the design of chiral ligands and organocatalysts.

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