(R)-1-(3,5-Bis(trifluoromethyl)phenyl)-N-methylethanamine(S)-2-Hydroxysuccinate


Chemical Name: (R)-1-(3,5-Bis(trifluoromethyl)phenyl)-N-methylethanamine(S)-2-Hydroxysuccinate
CAS Number: 935534-56-8
Product Number: AG00H2TZ(AGN-PC-0WAFIU)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties


Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



(S)-1-(3,5-Bis(trifluoromethyl)phenyl)-N-methylethanamine (S)-2-hydroxysuccinate is a key reagent in chemical synthesis, particularly in asymmetric synthesis and pharmaceutical research. This compound serves as a chiral building block, enabling the creation of enantiomerically pure molecules with high selectivity and efficiency.In chemical synthesis, (S)-1-(3,5-Bis(trifluoromethyl)phenyl)-N-methylethanamine (S)-2-hydroxysuccinate is commonly used as a resolving agent to separate racemic mixtures into their individual enantiomers. By exploiting the differences in reactivity between the two enantiomers, this compound allows for the isolation of pure enantiomers, which is crucial in drug development and the production of fine chemicals.Furthermore, (S)-1-(3,5-Bis(trifluoromethyl)phenyl)-N-methylethanamine (S)-2-hydroxysuccinate can also act as a ligand in asymmetric catalysis reactions, where it coordinates with metal catalysts to facilitate the formation of chiral products with high optical purity. This application is invaluable in the synthesis of pharmaceuticals and agrochemicals, where chirality plays a critical role in determining biological activity and efficacy.Overall, the unique properties of (S)-1-(3,5-Bis(trifluuoromethyl)phenyl)-N-methylethanamine (S)-2-hydroxysuccinate make it a versatile tool in chemical synthesis, opening up new possibilities for the development of complex molecules with precise stereochemistry.