(4S,4'S)-2,2'-(1,3-Bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-(tert-butyl)-4,5-dihydrooxazole)

98%

Reagent Code: #236850
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CAS Number 2283330-44-7

science Other reagents with same CAS 2283330-44-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 558.84 g/mol
Formula C₃₇H₅₄N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid structure and stereogenic centers make it effective in controlling the stereochemistry of reactions such as alkylations, aldol additions, and cycloadditions. Commonly employed with metal complexes like titanium or copper to promote high enantioselectivity in the synthesis of pharmaceuticals and fine chemicals. Valued for its ability to induce strong chiral induction and stability under various reaction conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,000.00
inventory 250mg
10-20 days ฿9,540.00
inventory 1g
10-20 days ฿30,780.00
(4S,4'S)-2,2'-(1,3-Bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-(tert-butyl)-4,5-dihydrooxazole)
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid structure and stereogenic centers make it effective in controlling the stereochemistry of reactions such as alkylations, aldol additions, and cycloadditions. Commonly employed with metal complexes like titanium or copper to promote high enantioselectivity in the synthesis of pharmaceuticals and fine chemicals. Valued for its ability to induce strong chiral induction and stability under var

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid structure and stereogenic centers make it effective in controlling the stereochemistry of reactions such as alkylations, aldol additions, and cycloadditions. Commonly employed with metal complexes like titanium or copper to promote high enantioselectivity in the synthesis of pharmaceuticals and fine chemicals. Valued for its ability to induce strong chiral induction and stability under various reaction conditions.

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