(S)-6,6'-Bis(4-chlorophenyl)-2,2',3,3'-tetrahydro-1,1'spirobi[1H-indene]-7,7'-diol

≥98%,99%e.e.

Reagent Code: #65656
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CAS Number 1258326-99-6

science Other reagents with same CAS 1258326-99-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 473.4 g/mol
Formula C₂₉H₂₂Cl₂O₂
thermostat Physical Properties
Melting Point 218-219 °C
Boiling Point 618.7±55.0 °C
inventory_2 Storage & Handling
Density 1.44±0.1 g/mL
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the development of chiral catalysts and ligands for asymmetric synthesis. Its unique structure, featuring a spirobiindane core, makes it highly effective in facilitating enantioselective reactions, which are crucial in the production of pharmaceuticals and fine chemicals. The presence of chlorophenyl groups enhances its stability and selectivity in catalytic processes. Additionally, it is employed in the synthesis of complex organic molecules, where its chiral environment ensures high enantiomeric purity in the final products. Its application extends to material science, where it is used in the design of advanced polymers and liquid crystals with specific optical properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿31,000.00

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(S)-6,6'-Bis(4-chlorophenyl)-2,2',3,3'-tetrahydro-1,1'spirobi[1H-indene]-7,7'-diol
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This compound is primarily utilized in the development of chiral catalysts and ligands for asymmetric synthesis. Its unique structure, featuring a spirobiindane core, makes it highly effective in facilitating enantioselective reactions, which are crucial in the production of pharmaceuticals and fine chemicals. The presence of chlorophenyl groups enhances its stability and selectivity in catalytic processes. Additionally, it is employed in the synthesis of complex organic molecules, where its chiral envir

This compound is primarily utilized in the development of chiral catalysts and ligands for asymmetric synthesis. Its unique structure, featuring a spirobiindane core, makes it highly effective in facilitating enantioselective reactions, which are crucial in the production of pharmaceuticals and fine chemicals. The presence of chlorophenyl groups enhances its stability and selectivity in catalytic processes. Additionally, it is employed in the synthesis of complex organic molecules, where its chiral environment ensures high enantiomeric purity in the final products. Its application extends to material science, where it is used in the design of advanced polymers and liquid crystals with specific optical properties.

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