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

≥95%,≥99%e.e.

Reagent Code: #59716
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CAS Number 137536-94-8

science Other reagents with same CAS 137536-94-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 666.8 g/mol
Formula C₄₇H₃₈O₄
thermostat Physical Properties
Boiling Point 200°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in the formation of carbon-carbon bonds, such as in asymmetric hydrogenation, alkylation, and Diels-Alder reactions. Its bulky naphthyl groups and rigid dioxolane structure make it effective in inducing stereochemical control, leading to the production of chiral compounds with high optical purity. Additionally, it finds application in the synthesis of pharmaceuticals and fine chemicals, where precise stereochemistry is critical for biological activity or material properties. Its use is also explored in the development of advanced materials, such as chiral polymers or catalysts for organic transformations.

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Test Parameter Specification
Appearance White powder
Purity 95-100
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿1,530.00
inventory 1g
10-20 days ฿6,960.00

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(4R,5R)-2,2-Dimethyl-α,α,α',α'-tetra(1-naphthyl)-1,3-dioxolane-4,5-dimethanol
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This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in the formation of carbon-carbon bonds, such as in asymmetric hydrogenation, alkylation, and Diels-Alder reactions. Its bulky naphthyl groups and rigid dioxolane structure make it effective in inducing stereochemical control, leading to the production of chiral compounds with high optical purity. Additionally, it finds application

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in the formation of carbon-carbon bonds, such as in asymmetric hydrogenation, alkylation, and Diels-Alder reactions. Its bulky naphthyl groups and rigid dioxolane structure make it effective in inducing stereochemical control, leading to the production of chiral compounds with high optical purity. Additionally, it finds application in the synthesis of pharmaceuticals and fine chemicals, where precise stereochemistry is critical for biological activity or material properties. Its use is also explored in the development of advanced materials, such as chiral polymers or catalysts for organic transformations.

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