(1S,2S)-N,N'-Dihydroxy-N,N'-bis(diphenylacetyl)cyclohexane-1,2-diamine


Chemical Name: (1S,2S)-N,N'-Dihydroxy-N,N'-bis(diphenylacetyl)cyclohexane-1,2-diamine
CAS Number: 1217464-22-6
Product Number: AG0015QI(AGN-PC-0WAFYN)
Synonyms:
MDL No:
Molecular Formula: C34H34N2O4
Molecular Weight: 534.6448

Identification/Properties


Properties
Storage:
Inert atmosphere;2-8℃;

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



N,N'-((1S,2S)-Cyclohexane-1,2-diyl)bis(N-hydroxy-2,2-diphenylacetamide), commonly referred to as $name$, plays a vital role in chemical synthesis as a versatile chiral ligand. This compound exhibits remarkable stereochemistry due to the presence of the cyclohexane backbone and the two hydroxy-diphenylacetamide units.In chemical synthesis, $name$ is utilized as a powerful ligand in asymmetric catalysis reactions. Its unique structure enables it to coordinate with a variety of metal ions, such as palladium, ruthenium, and rhodium, to form stable complexes. These complexes serve as efficient catalysts in a range of organic transformations, including cross-coupling reactions, hydrogenation reactions, and asymmetric cycloadditions.Moreover, the chiral nature of N,N'-((1S,2S)-Cyclohexane-1,2-diyl)bis(N-hydroxy-2,2-diphenylacetamide) imparts chirality to the metal catalyst, allowing for the enantioselective synthesis of valuable chiral molecules. This enables chemists to access enantiomerically pure compounds, which are essential in the pharmaceutical, agrochemical, and material science industries.Overall, the application of $name$ in chemical synthesis contributes significantly to the advancement of asymmetric catalysis, facilitating the efficient and selective synthesis of complex organic molecules with high levels of stereocontrol.