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CAS 1345413-20-8

:

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

Description:
The chemical substance known as (1S,2R)-2-(3,4-Difluorophenyl)-cyclopropanamine, with the CAS number 1345413-20-8, is characterized by its unique structural features and stereochemistry. It contains a cyclopropane ring, which is a three-membered carbon structure, and an amine functional group, indicating its potential as a basic compound. The presence of the 3,4-difluorophenyl group suggests that it has significant electron-withdrawing properties due to the fluorine atoms, which can influence its reactivity and interaction with biological targets. The specific stereochemistry, denoted by the (1S,2R) configuration, indicates the spatial arrangement of atoms around the chiral centers, which can affect the compound's pharmacological properties and biological activity. Such compounds are often of interest in medicinal chemistry for their potential therapeutic applications, particularly in the development of pharmaceuticals. Overall, this compound's unique characteristics make it a subject of interest for further research in various chemical and biological contexts.
Formula:C9H9F2N
Synonyms:
  • (1S,2R)-2-(3,4-Difluorophenyl)cyclopropan-1-amine
  • (1S,2R)-2-(3,4-difluorophenyl)cyclopropanamine
  • (1S,2R)-2-(3,4-Difluoro-phenyl)-cyclopropylamine
  • Ticagrelor Impurity 23 Mandelate
  • cis-2-(3,4-difluorophenyl) cyclopropanamine
  • ((1S,2R)-2-(3,4-Difluorophenyl)cyclopropanamine HCl)
  • trans-(1S,2R)-2-(3,4-difluorophenyl)-cyclopropylamine
  • (1S,2R)-2-(3,4-difluorophenyl)cyclopropanamine (S)-2-hydroxy-2-phenylacetate? (Ticagrelor Impurity）
  • (1S,2R)-2-(3,4-difluorophenyl)
  • Ticagrelor Related Compound VIII
  • Cyclopropanamine, 2-(3,4-difluorophenyl)-, (1S,2R)-
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