N-​[(11bS)​-​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

96%

Reagent Code: #57518
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CAS Number 1236120-02-7

science Other reagents with same CAS 1236120-02-7

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 asymmetric catalysis, particularly in organic synthesis processes where high enantioselectivity is required. It serves as a chiral ligand or catalyst in various reactions, including hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. Its unique structure, featuring trifluoromethyl groups, enhances its stability and reactivity in challenging environments, making it suitable for use in pharmaceutical synthesis to produce enantiomerically pure compounds. Additionally, it is employed in the development of advanced materials and fine chemicals, where precise control over molecular configuration is critical.

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Test Parameter Specification
APPEARANCE White to Off-white to Yellow Solid
Purity (%) 95.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿890.00
inventory 25mg
10-20 days ฿3,890.00
inventory 100mg
10-20 days ฿10,390.00
inventory 250mg
10-20 days ฿17,790.00

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N-​[(11bS)​-​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 asymmetric catalysis, particularly in organic synthesis processes where high enantioselectivity is required. It serves as a chiral ligand or catalyst in various reactions, including hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. Its unique structure, featuring trifluoromethyl groups, enhances its stability and reactivity in challenging environments, making it suitable for use in pharmaceutical synthesis to produce enantiomerically pure compounds. Additionally, it is employed in the development of advanced materials and fine chemicals, where precise control over molecular configuration is critical.
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