((4R,5R)-2,2-Dimethyl-1,3-dioxolane-4,5-diyl)bis(di(naphthalen-2-yl)methanol)

95%

Reagent Code: #231856
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CAS Number 137365-09-4

science Other reagents with same CAS 137365-09-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 666.80 g/mol
Formula C₄₇H₃₈O₄
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used as a chiral building block in asymmetric synthesis, particularly in the preparation of complex organic molecules requiring high enantiomeric purity. Its rigid dioxolane backbone and multiple hydroxyl groups make it suitable for use in stereoselective catalysis and as a scaffold in the development of chiral ligands or organocatalysts. Also employed in the synthesis of pharmaceutical intermediates where stereochemical control is critical. The naphthyl groups enhance lipophilicity and can aid in purification through chromatographic methods due to strong UV absorbance.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿15,410.00
inventory 1g
10-20 days ฿38,600.00
((4R,5R)-2,2-Dimethyl-1,3-dioxolane-4,5-diyl)bis(di(naphthalen-2-yl)methanol)
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Used as a chiral building block in asymmetric synthesis, particularly in the preparation of complex organic molecules requiring high enantiomeric purity. Its rigid dioxolane backbone and multiple hydroxyl groups make it suitable for use in stereoselective catalysis and as a scaffold in the development of chiral ligands or organocatalysts. Also employed in the synthesis of pharmaceutical intermediates where stereochemical control is critical. The naphthyl groups enhance lipophilicity and can aid in purifi

Used as a chiral building block in asymmetric synthesis, particularly in the preparation of complex organic molecules requiring high enantiomeric purity. Its rigid dioxolane backbone and multiple hydroxyl groups make it suitable for use in stereoselective catalysis and as a scaffold in the development of chiral ligands or organocatalysts. Also employed in the synthesis of pharmaceutical intermediates where stereochemical control is critical. The naphthyl groups enhance lipophilicity and can aid in purification through chromatographic methods due to strong UV absorbance.

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