(S)-4-Isopropyl-2-(1,10-phenanthrolin-2-yl)-4,5-dihydrooxazole

98%

Reagent Code: #38511
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CAS Number 1562372-40-0

science Other reagents with same CAS 1562372-40-0

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Weight 291.3471 g/mol
Formula C₁₈H₁₇N₃O
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description Product Description

This compound is primarily utilized in asymmetric catalysis, particularly in enantioselective synthesis, where it serves as a chiral ligand. Its structure, featuring a phenanthroline moiety and an oxazoline ring, makes it effective in coordinating with metal ions, such as copper or palladium, to form stable complexes. These complexes are employed in various organic transformations, including cyclopropanation, allylic alkylation, and Diels-Alder reactions, where high enantioselectivity is required. Additionally, it finds application in the development of chiral catalysts for pharmaceutical synthesis, enabling the production of enantiomerically pure compounds. Its stability and efficiency in catalytic systems make it a valuable tool in the field of organic and medicinal chemistry.

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inventory 100mg
10-20 days ฿9,702.00

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(S)-4-Isopropyl-2-(1,10-phenanthrolin-2-yl)-4,5-dihydrooxazole
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This compound is primarily utilized in asymmetric catalysis, particularly in enantioselective synthesis, where it serves as a chiral ligand. Its structure, featuring a phenanthroline moiety and an oxazoline ring, makes it effective in coordinating with metal ions, such as copper or palladium, to form stable complexes. These complexes are employed in various organic transformations, including cyclopropanation, allylic alkylation, and Diels-Alder reactions, where high enantioselectivity is required. Additi

This compound is primarily utilized in asymmetric catalysis, particularly in enantioselective synthesis, where it serves as a chiral ligand. Its structure, featuring a phenanthroline moiety and an oxazoline ring, makes it effective in coordinating with metal ions, such as copper or palladium, to form stable complexes. These complexes are employed in various organic transformations, including cyclopropanation, allylic alkylation, and Diels-Alder reactions, where high enantioselectivity is required. Additionally, it finds application in the development of chiral catalysts for pharmaceutical synthesis, enabling the production of enantiomerically pure compounds. Its stability and efficiency in catalytic systems make it a valuable tool in the field of organic and medicinal chemistry.

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