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CAS 1156491-10-9

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(1R trans)-2-(3,4-difluorophenyl)cyclopropane amine hydrochloride

Description:
(1R trans)-2-(3,4-difluorophenyl)cyclopropane amine hydrochloride is a chemical compound characterized by its unique cyclopropane structure, which is a three-membered carbon ring. The presence of a difluorophenyl group indicates that the compound has two fluorine atoms substituted on a phenyl ring, enhancing its lipophilicity and potentially influencing its biological activity. The amine functional group suggests that it can participate in hydrogen bonding, which may affect its solubility and reactivity. As a hydrochloride salt, it is typically more stable and soluble in water compared to its free base form, making it suitable for pharmaceutical applications. The specific stereochemistry indicated by the (1R trans) designation implies a particular spatial arrangement of atoms, which can be crucial for the compound's interaction with biological targets. Overall, this compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry and drug development.
Formula:C9H9F2N・ClH
InChI:InChI=1S/C9H9F2N.ClH/c10-7-2-1-5(3-8(7)11)6-4-9(6)12;/h1-3,6,9H,4,12H2;1H/t6?,9-;/m1./s1
SMILES:c1cc(c(cc1C1C[C@H]1N)F)F.Cl
Synonyms:
  • (1R,2S)-Rel-2-(3,4-Difluorophenyl)Cyclopropanamine Hydrochloride
  • (1R,2S)-2-(3,4-difluorophenyl)cyclopropanamine hydrochloride
  • (1R,2S)-rel-2-(3,4-Difluorophenyl)cyclopropanamine HCl
  • (1R,2S)-2-(3,4-difluorophenyl)cyclopropanamine HCL
  • (1R,2S)-rel-2-(3,4-Difluoro phenyl)cyclopropanamine hydrochloride
  • (1R trans)-2-(3,4-difluorophenyl)cyclopropane amine
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