(4S,5S)-2,2-Dimethyl-α,α,α',α'-tetra(1-naphthyl)-1,3-dioxolane-4,5-dimethanol

≥95%,≥99%e.e.

Reagent Code: #59740
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CAS Number 171086-52-5

science Other reagents with same CAS 171086-52-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 666.8 g/mol
Formula C₄₇H₃₈O₄
thermostat Physical Properties
Boiling Point 201°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in asymmetric synthesis as a chiral auxiliary or ligand. Its unique structure, featuring multiple naphthyl groups, makes it highly effective in inducing chirality in organic reactions, particularly in stereoselective transformations. It is often employed in catalytic systems to enhance enantioselectivity in the synthesis of complex molecules, such as pharmaceuticals or fine chemicals. The compound’s rigid framework and steric properties allow for precise control over the spatial arrangement of reactants, leading to the formation of specific enantiomers with high purity. Additionally, it can be used in the development of chiral catalysts for applications in industrial chemical processes, where achieving high enantiomeric excess is critical. Its role in facilitating asymmetric hydrogenation, epoxidation, and other key reactions makes it a valuable tool in synthetic organic chemistry.

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Test Parameter Specification
Appearance solid
Purity 94.5-100
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿800.00
inventory 1g
10-20 days ฿2,600.00
inventory 5g
10-20 days ฿9,650.00

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(4S,5S)-2,2-Dimethyl-α,α,α',α'-tetra(1-naphthyl)-1,3-dioxolane-4,5-dimethanol
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This chemical is primarily utilized in asymmetric synthesis as a chiral auxiliary or ligand. Its unique structure, featuring multiple naphthyl groups, makes it highly effective in inducing chirality in organic reactions, particularly in stereoselective transformations. It is often employed in catalytic systems to enhance enantioselectivity in the synthesis of complex molecules, such as pharmaceuticals or fine chemicals. The compound’s rigid framework and steric properties allow for precise control over t

This chemical is primarily utilized in asymmetric synthesis as a chiral auxiliary or ligand. Its unique structure, featuring multiple naphthyl groups, makes it highly effective in inducing chirality in organic reactions, particularly in stereoselective transformations. It is often employed in catalytic systems to enhance enantioselectivity in the synthesis of complex molecules, such as pharmaceuticals or fine chemicals. The compound’s rigid framework and steric properties allow for precise control over the spatial arrangement of reactants, leading to the formation of specific enantiomers with high purity. Additionally, it can be used in the development of chiral catalysts for applications in industrial chemical processes, where achieving high enantiomeric excess is critical. Its role in facilitating asymmetric hydrogenation, epoxidation, and other key reactions makes it a valuable tool in synthetic organic chemistry.

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