(S)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-bis([1,1':3',1''-terphenyl]-5'-yl)-[1,1'-binaphthalene]-2,2'-diol

≥98%,99%e.e.

Reagent Code: #65639
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CAS Number 1496637-08-1

science Other reagents with same CAS 1496637-08-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 751 g/mol
Formula C₅₆H₄₆O₂
inventory_2 Storage & Handling
Density 1.179±0.06 g/mL
Storage room temperature, dry

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in the development of pharmaceuticals, where the precise control of stereochemistry is crucial for the efficacy and safety of the drug. Additionally, it finds application in the synthesis of complex organic molecules, including natural products and fine chemicals, where its ability to induce chirality enhances the yield and purity of the desired enantiomer. Its robust structure and high selectivity make it a valuable tool in advanced organic synthesis and industrial chemistry.

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Test Parameter Specification
Appearance off-white powder
Purity (%) 98-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,580.00

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(S)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-bis([1,1':3',1''-terphenyl]-5'-yl)-[1,1'-binaphthalene]-2,2'-diol
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This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in the development of pharmaceuticals, where the precise control of stereochemistry is crucial for the efficacy and safety of the drug. Additionally, it finds application in the synthesis of complex organic molecules, including natural products and fine chemicals, where its ability to induce chirality enhances the yield and pur

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in the development of pharmaceuticals, where the precise control of stereochemistry is crucial for the efficacy and safety of the drug. Additionally, it finds application in the synthesis of complex organic molecules, including natural products and fine chemicals, where its ability to induce chirality enhances the yield and purity of the desired enantiomer. Its robust structure and high selectivity make it a valuable tool in advanced organic synthesis and industrial chemistry.

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