(R)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-bis(4-methoxyphenyl)-[1,1'-binaphthalene]-2,2'-diol

≥98%,99%e.e.

Reagent Code: #70339
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CAS Number 1011465-19-2

science Other reagents with same CAS 1011465-19-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 506.6 g/mol
Formula C₃₄H₃₄O₄
thermostat Physical Properties
Melting Point 167-169 °C
Boiling Point 676.4±55.0 °C
inventory_2 Storage & Handling
Density 1.195±0.06 g/mL
Storage room temperature, dry

description Product Description

This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in transition metal-catalyzed processes, such as hydrogenation, carbon-carbon bond formation, and other transformations where controlling the stereochemistry of the product is critical. Its rigid binaphthyl backbone and methoxy substituents enhance its ability to induce chirality, making it valuable in the production of pharmaceuticals, fine chemicals, and agrochemicals. Additionally, it is used in the development of chiral catalysts and materials for applications in organic electronics and advanced materials science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,400.00

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(R)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-bis(4-methoxyphenyl)-[1,1'-binaphthalene]-2,2'-diol
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This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in transition metal-catalyzed processes, such as hydrogenation, carbon-carbon bond formation, and other transformations where controlling the stereochemistry of the product is critical. Its rigid binaphthyl backbone and methoxy substituents enhance its ability to induce chirality, making it valuable in the production of pharmac

This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in transition metal-catalyzed processes, such as hydrogenation, carbon-carbon bond formation, and other transformations where controlling the stereochemistry of the product is critical. Its rigid binaphthyl backbone and methoxy substituents enhance its ability to induce chirality, making it valuable in the production of pharmaceuticals, fine chemicals, and agrochemicals. Additionally, it is used in the development of chiral catalysts and materials for applications in organic electronics and advanced materials science.

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