(11bS)-4-Hydroxy-2,6-bis[4-(trifluoromethyl)phenyl]-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin

≥98%,99%e.e.

Reagent Code: #70508
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CAS Number 1264573-23-0

science Other reagents with same CAS 1264573-23-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 636.5 g/mol
Formula C₃₄H₁₉F₆O₄P
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring trifluoromethyl groups and a dioxaphosphepin ring, makes it highly effective in facilitating enantioselective transformations, which are crucial for producing optically active compounds. These compounds are often intermediates in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its stability and reactivity under various conditions make it a valuable tool in advanced research and industrial processes aiming to achieve high selectivity and yield in complex organic reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,357.00
inventory 250mg
10-20 days ฿6,894.00
inventory 1g
10-20 days ฿21,798.00

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(11bS)-4-Hydroxy-2,6-bis[4-(trifluoromethyl)phenyl]-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin
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This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring trifluoromethyl groups and a dioxaphosphepin ring, makes it highly effective in facilitating enantioselective transformations, which are crucial for producing optically active compounds. These compounds are often intermediates in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its stability and reacti

This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring trifluoromethyl groups and a dioxaphosphepin ring, makes it highly effective in facilitating enantioselective transformations, which are crucial for producing optically active compounds. These compounds are often intermediates in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its stability and reactivity under various conditions make it a valuable tool in advanced research and industrial processes aiming to achieve high selectivity and yield in complex organic reactions.

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