N-​[(11bR)​-​2,​6-​Bis[3,​5-​bis(trifluoromethyl)​phenyl]​-​4-​oxido-dinaphtho[2,​1-​d:1',​2'-​f]​[1,​3,​2]​dioxaphosphepin-​4-​yl]​-​1,​1,​1-​trifluoromethanesulfonamide

≥98%,≥99% e.e.

Reagent Code: #57501
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CAS Number 1010800-02-8

science Other reagents with same CAS 1010800-02-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 903.6 g/mol
Formula C₃₇H₁₇F₁₅NO₅PS
thermostat Physical Properties
Boiling Point 740.7±70.0 °C
inventory_2 Storage & Handling
Density 1.70±0.1 g/mL
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in advanced organic synthesis, particularly in asymmetric catalysis. Its structure, featuring trifluoromethyl groups and a phosphine oxide moiety, makes it highly effective as a chiral ligand or catalyst in enantioselective reactions. It is often employed in the synthesis of complex pharmaceutical intermediates, where high stereochemical control is required. Additionally, its electron-withdrawing groups enhance its stability and reactivity in challenging chemical environments, making it suitable for use in the development of fine chemicals and specialty materials. Its application extends to the field of agrochemicals, where it aids in the creation of optically active compounds with improved efficacy.

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Test Parameter Specification
Appearance White to Off-White Solid
Purity 98-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,810.00
inventory 250mg
10-20 days ฿10,650.00

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N-​[(11bR)​-​2,​6-​Bis[3,​5-​bis(trifluoromethyl)​phenyl]​-​4-​oxido-dinaphtho[2,​1-​d:1',​2'-​f]​[1,​3,​2]​dioxaphosphepin-​4-​yl]​-​1,​1,​1-​trifluoromethanesulfonamide
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This chemical is primarily utilized in advanced organic synthesis, particularly in asymmetric catalysis. Its structure, featuring trifluoromethyl groups and a phosphine oxide moiety, makes it highly effective as a chiral ligand or catalyst in enantioselective reactions. It is often employed in the synthesis of complex pharmaceutical intermediates, where high stereochemical control is required. Additionally, its electron-withdrawing groups enhance its stability and reactivity in challenging chemical envir

This chemical is primarily utilized in advanced organic synthesis, particularly in asymmetric catalysis. Its structure, featuring trifluoromethyl groups and a phosphine oxide moiety, makes it highly effective as a chiral ligand or catalyst in enantioselective reactions. It is often employed in the synthesis of complex pharmaceutical intermediates, where high stereochemical control is required. Additionally, its electron-withdrawing groups enhance its stability and reactivity in challenging chemical environments, making it suitable for use in the development of fine chemicals and specialty materials. Its application extends to the field of agrochemicals, where it aids in the creation of optically active compounds with improved efficacy.

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