(4R,4'R)-2,2'-(1-Phenylpropane-2,2-diyl)bis(4-phenyl-4,5-dihydrooxazole)

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Reagent Code: #231379
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CAS Number 2757082-35-0

science Other reagents with same CAS 2757082-35-0

blur_circular Chemical Specifications

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Weight 410.51 g/mol
Formula C₂₇H₂₆N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its structure enables effective stereocontrol in reactions such as aldol condensations, alkylations, and cycloadditions. Commonly employed with metal complexes like copper(II) or nickel(II) to form catalysts that promote high enantioselectivity in the synthesis of pharmaceutical intermediates and fine chemicals. Valued for its ability to induce chirality in carbon–carbon bond-forming reactions, making it useful in the development of optically active compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,370.00
inventory 250mg
10-20 days ฿5,690.00
inventory 1g
10-20 days ฿22,740.00

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(4R,4'R)-2,2'-(1-Phenylpropane-2,2-diyl)bis(4-phenyl-4,5-dihydrooxazole)
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its structure enables effective stereocontrol in reactions such as aldol condensations, alkylations, and cycloadditions. Commonly employed with metal complexes like copper(II) or nickel(II) to form catalysts that promote high enantioselectivity in the synthesis of pharmaceutical intermediates and fine chemicals. Valued for its ability to induce chirality in carbon–carbon bond-forming reactions, maki

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its structure enables effective stereocontrol in reactions such as aldol condensations, alkylations, and cycloadditions. Commonly employed with metal complexes like copper(II) or nickel(II) to form catalysts that promote high enantioselectivity in the synthesis of pharmaceutical intermediates and fine chemicals. Valued for its ability to induce chirality in carbon–carbon bond-forming reactions, making it useful in the development of optically active compounds.

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