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CAS 185225-84-7

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Cyclopropanamine, 2-fluoro-, (1S,2R)-, 4-methylbenzenesulfonate

Description:
Cyclopropanamine, 2-fluoro-, (1S,2R)-, 4-methylbenzenesulfonate is a chemical compound characterized by its unique cyclopropane structure, which contributes to its reactivity and potential applications in medicinal chemistry. The presence of a fluorine atom at the 2-position of the cyclopropanamine moiety enhances its biological activity and lipophilicity, potentially influencing its interaction with biological targets. The (1S,2R) stereochemistry indicates specific spatial arrangements of atoms, which can significantly affect the compound's pharmacological properties. The 4-methylbenzenesulfonate group serves as a leaving group and may enhance solubility in various solvents, making it suitable for different chemical reactions or formulations. This compound may exhibit interesting properties such as selective binding to certain receptors or enzymes, making it a candidate for further research in drug development. As with many amines, it may also participate in hydrogen bonding, influencing its behavior in biological systems. Overall, the combination of its structural features suggests potential utility in pharmaceutical applications, although specific biological activities would require empirical investigation.
Formula:C7H8O3S·C3H6FN
InChI:InChI=1S/C7H8O3S.C3H6FN/c1-6-2-4-7(5-3-6)11(8,9)10;4-2-1-3(2)5/h2-5H,1H3,(H,8,9,10);2-3H,1,5H2/t;2-,3+/m.1/s1
InChI key:InChIKey=XUWZMHVPMZXIRU-RCROYASPSA-N
SMILES:F[C@H]1[C@@H](N)C1.S(=O)(=O)(O)C1=CC=C(C)C=C1
Synonyms:
  • Cyclopropanamine, 2-fluoro-, (1S-cis)-, 4-methylbenzenesulfonate
  • Cyclopropanamine, 2-fluoro-, (1S,2R)-, 4-methylbenzenesulfonate
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