(S)-3,3'-Bis(4-chlorophenyl)-5,5',6,6',7,7',8,8'-octahydro-[1,1'-binaphthalene]-2,2'-diol

≥95%,≥99%e.e.

Reagent Code: #70514

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 515.5 g/mol
Formula C₃₂H₂₈Cl₂O₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand or catalyst. It is particularly effective in facilitating enantioselective reactions, which are crucial for producing optically active compounds in pharmaceuticals and fine chemicals. Its robust structure and chiral environment make it suitable for applications in hydrogenation, carbon-carbon bond formation, and other catalytic processes. Additionally, it is employed in the development of advanced materials and in research focused on understanding chiral induction mechanisms.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,440.00

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(S)-3,3'-Bis(4-chlorophenyl)-5,5',6,6',7,7',8,8'-octahydro-[1,1'-binaphthalene]-2,2'-diol
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This chemical is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand or catalyst. It is particularly effective in facilitating enantioselective reactions, which are crucial for producing optically active compounds in pharmaceuticals and fine chemicals. Its robust structure and chiral environment make it suitable for applications in hydrogenation, carbon-carbon bond formation, and other catalytic processes. Additionally, it is employed in the development of advanced

This chemical is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand or catalyst. It is particularly effective in facilitating enantioselective reactions, which are crucial for producing optically active compounds in pharmaceuticals and fine chemicals. Its robust structure and chiral environment make it suitable for applications in hydrogenation, carbon-carbon bond formation, and other catalytic processes. Additionally, it is employed in the development of advanced materials and in research focused on understanding chiral induction mechanisms.

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