(11bS)​-2,​6-Bis(4-​chlorophenyl)​-​4-​hydroxy-4-​oxide-dinaphtho[2,​1-​d:1',​2'-​f]​[1,​3,​2]​dioxaphosphepin

≥98%,≥99%e.e.

Reagent Code: #70513

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 569.4 g/mol
Formula C₃₂H₁₉Cl₂O₄P
thermostat Physical Properties
Boiling Point 786.7±70.0 °C
inventory_2 Storage & Handling
Density 1.53±0.1 g/mL
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 a dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin core, makes it effective in controlling stereochemistry during the formation of complex molecules. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where precise enantiomeric control is crucial. Additionally, its ability to form stable complexes with transition metals enhances its utility in catalytic processes, such as hydrogenation, cross-coupling, and cyclization reactions. Its application in these areas contributes to the development of more efficient and selective synthetic methodologies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿21,861.00

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(11bS)​-2,​6-Bis(4-​chlorophenyl)​-​4-​hydroxy-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 a dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin core, makes it effective in controlling stereochemistry during the formation of complex molecules. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where precise enantiomeric control is crucial. Additionally, its ability to form stable complexes with transitio

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 a dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin core, makes it effective in controlling stereochemistry during the formation of complex molecules. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where precise enantiomeric control is crucial. Additionally, its ability to form stable complexes with transition metals enhances its utility in catalytic processes, such as hydrogenation, cross-coupling, and cyclization reactions. Its application in these areas contributes to the development of more efficient and selective synthetic methodologies.

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