(4S,4'S,5R,5'R)-2,2'-cyclopropylidenebis[4,5-dihydro-4,5-diphenyl-Oxazole

98%

Reagent Code: #59739
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CAS Number 229184-97-8

science Other reagents with same CAS 229184-97-8

blur_circular Chemical Specifications

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Weight 484.59 g/mol
Formula C₃₃H₂₈N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, featuring a cyclopropylidene bridge and diphenyloxazole moieties, makes it highly effective in inducing chirality in catalytic reactions. It is often employed in enantioselective transformations, such as hydrogenation, cyclopropanation, and carbon-carbon bond-forming reactions, which are crucial in the synthesis of pharmaceuticals and fine chemicals. Additionally, its rigid framework and stereochemical properties enhance the selectivity and efficiency of catalytic processes, making it a valuable tool in organic synthesis for producing optically active compounds.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿3,735.00
inventory 50mg
10-20 days ฿14,940.00

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(4S,4'S,5R,5'R)-2,2'-cyclopropylidenebis[4,5-dihydro-4,5-diphenyl-Oxazole
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This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, featuring a cyclopropylidene bridge and diphenyloxazole moieties, makes it highly effective in inducing chirality in catalytic reactions. It is often employed in enantioselective transformations, such as hydrogenation, cyclopropanation, and carbon-carbon bond-forming reactions, which are crucial in the synthesis of pharmaceutica

This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, featuring a cyclopropylidene bridge and diphenyloxazole moieties, makes it highly effective in inducing chirality in catalytic reactions. It is often employed in enantioselective transformations, such as hydrogenation, cyclopropanation, and carbon-carbon bond-forming reactions, which are crucial in the synthesis of pharmaceuticals and fine chemicals. Additionally, its rigid framework and stereochemical properties enhance the selectivity and efficiency of catalytic processes, making it a valuable tool in organic synthesis for producing optically active compounds.

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