(4R,4'R)-4,4'-Di((S)-sec-butyl)-4,4',5,5'-tetrahydro-2,2'-bioxazole

98%

Reagent Code: #36969
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CAS Number 2270178-41-9

science Other reagents with same CAS 2270178-41-9

blur_circular Chemical Specifications

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Weight 252.3526 g/mol
Formula C₁₄H₂₄N₂O₂
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, featuring bioxazole rings and sec-butyl groups, makes it highly effective in enantioselective reactions, such as hydrogenation, allylic alkylation, and cross-coupling reactions. It is also employed in the synthesis of biologically active molecules and pharmaceuticals, where precise control over stereochemistry is crucial. Additionally, it serves as a building block in organic synthesis for constructing complex molecular architectures with high stereochemical fidelity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,992.00
inventory 500mg
10-20 days ฿32,290.00

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(4R,4'R)-4,4'-Di((S)-sec-butyl)-4,4',5,5'-tetrahydro-2,2'-bioxazole
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This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, featuring bioxazole rings and sec-butyl groups, makes it highly effective in enantioselective reactions, such as hydrogenation, allylic alkylation, and cross-coupling reactions. It is also employed in the synthesis of biologically active molecules and pharmaceuticals, where precise control over stereochemistry is crucial. Additi

This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, featuring bioxazole rings and sec-butyl groups, makes it highly effective in enantioselective reactions, such as hydrogenation, allylic alkylation, and cross-coupling reactions. It is also employed in the synthesis of biologically active molecules and pharmaceuticals, where precise control over stereochemistry is crucial. Additionally, it serves as a building block in organic synthesis for constructing complex molecular architectures with high stereochemical fidelity.

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