(4R,4'R)-2,2'-(1,3-Diphenylpropane-2,2-diyl)bis(4-methyl-4,5-dihydrooxazole)

97%

Reagent Code: #231360
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CAS Number 2634687-66-2

science Other reagents with same CAS 2634687-66-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 362.46 g/mol
Formula C₂₃H₂₆N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral ligand in asymmetric synthesis, enabling high enantioselectivity in organic reactions such as aldol condensations and alkylations. Its rigid structure and stereochemical stability make it valuable for controlling the formation of chiral centers in complex molecule synthesis, particularly in pharmaceuticals and fine chemicals. Commonly employed in transition metal-catalyzed reactions to induce chirality, it can be recovered and reused after the reaction, improving process efficiency. Also applied in the development of enantiopure ligands for catalysis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿4,370.00
250mg
10-20 days ฿10,570.00
1g
10-20 days ฿42,250.00
(4R,4'R)-2,2'-(1,3-Diphenylpropane-2,2-diyl)bis(4-methyl-4,5-dihydrooxazole)
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Used as a chiral ligand in asymmetric synthesis, enabling high enantioselectivity in organic reactions such as aldol condensations and alkylations. Its rigid structure and stereochemical stability make it valuable for controlling the formation of chiral centers in complex molecule synthesis, particularly in pharmaceuticals and fine chemicals. Commonly employed in transition metal-catalyzed reactions to induce chirality, it can be recovered and reused after the reaction, improving process efficiency. Also

Used as a chiral ligand in asymmetric synthesis, enabling high enantioselectivity in organic reactions such as aldol condensations and alkylations. Its rigid structure and stereochemical stability make it valuable for controlling the formation of chiral centers in complex molecule synthesis, particularly in pharmaceuticals and fine chemicals. Commonly employed in transition metal-catalyzed reactions to induce chirality, it can be recovered and reused after the reaction, improving process efficiency. Also applied in the development of enantiopure ligands for catalysis.

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