(R)-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: #70336
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CAS Number 915038-18-5

science Other reagents with same CAS 915038-18-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 515.5 g/mol
Formula C₃₂H₂₈Cl₂O₂
thermostat Physical Properties
Boiling Point 664.3±55.0 °C
inventory_2 Storage & Handling
Density 1.289±0.06 g/mL
Storage room temperature, dry

description Product Description

This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in facilitating enantioselective reactions, particularly in the production of pharmaceuticals and fine chemicals where precise stereochemistry is crucial. Its structure allows it to effectively induce chirality in reactions such as hydrogenation, oxidation, and carbon-carbon bond formation. Additionally, it is employed in the development of advanced materials and in research focused on understanding chiral induction mechanisms. Its stability and selectivity make it a valuable tool in organic synthesis and industrial applications requiring high enantiomeric purity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿20,080.00

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(R)-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 compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in facilitating enantioselective reactions, particularly in the production of pharmaceuticals and fine chemicals where precise stereochemistry is crucial. Its structure allows it to effectively induce chirality in reactions such as hydrogenation, oxidation, and carbon-carbon bond formation. Additionally, it is employed in the development of advanced materials and in research focused on understanding chiral induction mechanisms. Its stability and selectivity make it a valuable tool in organic synthesis and industrial applications requiring high enantiomeric purity.
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