(S)-3,3'-Bis[4-(trifluoromethyl)phenyl]-[1,1'-binaphthalene]-2,2'-diol

98%, ee 99%

Reagent Code: #38352
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CAS Number 1621066-21-4

science Other reagents with same CAS 1621066-21-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 574.5118192 g/mol
Formula C₃₄H₂₀F₆O₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions such as hydrogenation, allylic alkylation, and Diels-Alder reactions. Its ability to induce chirality in products makes it valuable in the production of enantiomerically pure pharmaceuticals and fine chemicals. Additionally, it is employed in the development of chiral catalysts for organic transformations, enhancing selectivity and efficiency in complex synthetic pathways. Its robust structure and high enantioselectivity also make it suitable for use in materials science, particularly in the design of chiral polymers and liquid crystals.

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Size Availability Unit Price Quantity
inventory 5 mg
10-20 days ฿720.00
inventory 25 mg
10-20 days ฿1,530.00
inventory 100 mg
10-20 days ฿2,700.00

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(S)-3,3'-Bis[4-(trifluoromethyl)phenyl]-[1,1'-binaphthalene]-2,2'-diol
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This chemical is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions such as hydrogenation, allylic alkylation, and Diels-Alder reactions. Its ability to induce chirality in products makes it valuable in the production of enantiomerically pure pharmaceuticals and fine chemicals. Additionally, it is employed in the development of chiral catalysts for organic transformations, enhancing selectivity and efficiency in complex synthetic pathways. Its robust structure and

This chemical is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions such as hydrogenation, allylic alkylation, and Diels-Alder reactions. Its ability to induce chirality in products makes it valuable in the production of enantiomerically pure pharmaceuticals and fine chemicals. Additionally, it is employed in the development of chiral catalysts for organic transformations, enhancing selectivity and efficiency in complex synthetic pathways. Its robust structure and high enantioselectivity also make it suitable for use in materials science, particularly in the design of chiral polymers and liquid crystals.

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