N-​[(11bR)​-​2,​6-​Di-​9-​anthracenyl-​8,​9,​10,​11,​12,​13,​14,​15-​octahydro-​8-​oxidodinaphtho[2,​1-​d:1',​2'-​f]​[1,​3,​2]​dioxaphosphepin-​4-​yl]​-​1,​1,​1-​trifluoromethanesulfonamide

≥98%,≥99% e.e.

Reagent Code: #57513
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CAS Number 1227374-65-3

science Other reagents with same CAS 1227374-65-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 839.9 g/mol
Formula C₄₉H₃₇F₃NO₅PS
inventory_2 Storage & Handling
Density 1.49±0.1 g/mL
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the field of organic synthesis and catalysis. It serves as a highly effective chiral ligand in asymmetric catalytic reactions, particularly in the synthesis of enantiomerically pure compounds. Its unique structure and steric properties make it valuable for controlling the stereochemistry of complex organic transformations, such as hydrogenation, carbon-carbon bond formation, and other pivotal reactions in pharmaceutical and fine chemical production. Additionally, its trifluoromethanesulfonamide moiety enhances its stability and reactivity, making it suitable for use in demanding reaction conditions. Its application is particularly significant in the development of chiral drugs and intermediates, where precise stereocontrol is critical.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,860.00

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N-​[(11bR)​-​2,​6-​Di-​9-​anthracenyl-​8,​9,​10,​11,​12,​13,​14,​15-​octahydro-​8-​oxidodinaphtho[2,​1-​d:1',​2'-​f]​[1,​3,​2]​dioxaphosphepin-​4-​yl]​-​1,​1,​1-​trifluoromethanesulfonamide
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This compound is primarily utilized in the field of organic synthesis and catalysis. It serves as a highly effective chiral ligand in asymmetric catalytic reactions, particularly in the synthesis of enantiomerically pure compounds. Its unique structure and steric properties make it valuable for controlling the stereochemistry of complex organic transformations, such as hydrogenation, carbon-carbon bond formation, and other pivotal reactions in pharmaceutical and fine chemical production. Additionally, it

This compound is primarily utilized in the field of organic synthesis and catalysis. It serves as a highly effective chiral ligand in asymmetric catalytic reactions, particularly in the synthesis of enantiomerically pure compounds. Its unique structure and steric properties make it valuable for controlling the stereochemistry of complex organic transformations, such as hydrogenation, carbon-carbon bond formation, and other pivotal reactions in pharmaceutical and fine chemical production. Additionally, its trifluoromethanesulfonamide moiety enhances its stability and reactivity, making it suitable for use in demanding reaction conditions. Its application is particularly significant in the development of chiral drugs and intermediates, where precise stereocontrol is critical.

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