(1S,2R)-2-(3,4-Difluorophenyl)cyclopropanamine


Chemical Name: (1S,2R)-2-(3,4-Difluorophenyl)cyclopropanamine
CAS Number: 1345413-20-8
Product Number: AG009GH3(AGN-PC-0WAGSA)
Synonyms:
MDL No:
Molecular Formula: C9H9F2N
Molecular Weight: 169.1712664

Identification/Properties


Safety Information


GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


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Chemical Structure



(1S,2R)-2-(3,4-Difluorophenyl)cyclopropanamine is a valuable compound widely utilized in chemical synthesis as a versatile building block and chiral intermediate. Its unique stereochemistry, with a chiral center at the 2nd carbon and a difluorophenyl group attached to the cyclopropane ring, allows for precise control over the stereochemical outcomes of various reactions.In synthetic chemistry, (1S,2R)-2-(3,4-Difluorophenyl)cyclopropanamine is commonly employed in the preparation of complex molecules and pharmaceuticals due to its ability to impart chirality and influence the overall three-dimensional shape of the target molecules. By incorporating this compound into synthetic pathways, chemists can access enantiomerically pure compounds with high levels of stereocontrol.Furthermore, the unique structural features of (1S,2R)-2-(3,4-Difluorophenyl)cyclopropanamine make it a valuable tool in the development of new chemical methodologies and asymmetric synthesis strategies. Its presence can facilitate the formation of key chemical bonds, enable the creation of stereocenters, and enhance the overall efficiency of the synthetic process.Overall, the application of (1S,2R)-2-(3,4-Difluorophenyl)cyclopropanamine in chemical synthesis is instrumental in advancing the field of organic chemistry by enabling the construction of complex molecules with high levels of stereochemical control and enhancing the diversity of chemical structures accessible to synthetic chemists.