(S)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-di-9-phenanthrenyl-[1,1'-binaphthalene]-2,2'-diol

≥95%,99%e.e.

Reagent Code: #65638
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CAS Number 1028416-48-9

science Other reagents with same CAS 1028416-48-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 646.8 g/mol
Formula C₄₈H₃₈O₂
inventory_2 Storage & Handling
Density 1.262±0.06 g/mL
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure allows it to effectively induce chirality in various organic reactions, such as hydrogenation, carbon-carbon bond formation, and oxidation processes. It is also employed in the synthesis of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for producing drugs with high stereochemical precision. Additionally, it finds application in materials science for creating chiral polymers and advanced molecular frameworks with specific optical properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,860.00

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(S)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-di-9-phenanthrenyl-[1,1'-binaphthalene]-2,2'-diol
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This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure allows it to effectively induce chirality in various organic reactions, such as hydrogenation, carbon-carbon bond formation, and oxidation processes. It is also employed in the synthesis of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for producing drugs with high stereochemical precision. Add

This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure allows it to effectively induce chirality in various organic reactions, such as hydrogenation, carbon-carbon bond formation, and oxidation processes. It is also employed in the synthesis of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for producing drugs with high stereochemical precision. Additionally, it finds application in materials science for creating chiral polymers and advanced molecular frameworks with specific optical properties.

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