Your browser doesn't support javascript.
loading
Characterization of the synthetic cannabinoid MDMB-CHMCZCA.
Weber, Carina; Pusch, Stefan; Schollmeyer, Dieter; Münster-Müller, Sascha; Pütz, Michael; Opatz, Till.
Afiliación
  • Weber C; Johannes Gutenberg University Mainz, Institute of Organic Chemistry, Duesbergweg 10-14, 55128 Mainz, Germany.
  • Pusch S; Johannes Gutenberg University Mainz, Institute of Organic Chemistry, Duesbergweg 10-14, 55128 Mainz, Germany.
  • Schollmeyer D; Johannes Gutenberg University Mainz, Institute of Organic Chemistry, Duesbergweg 10-14, 55128 Mainz, Germany.
  • Münster-Müller S; Bundeskriminalamt - Federal Criminal Police Office (BKA), Forensic Science Institute, KT 45 - Toxicology, Äppelallee 45, 65203 Wiesbaden, Germany.
  • Pütz M; Bundeskriminalamt - Federal Criminal Police Office (BKA), Forensic Science Institute, KT 45 - Toxicology, Äppelallee 45, 65203 Wiesbaden, Germany.
  • Opatz T; Johannes Gutenberg University Mainz, Institute of Organic Chemistry, Duesbergweg 10-14, 55128 Mainz, Germany.
Beilstein J Org Chem ; 12: 2808-2815, 2016.
Article en En | MEDLINE | ID: mdl-28144353
The synthetic cannabinoid MDMB-CHMCZCA was characterized by various spectroscopic techniques including NMR spectroscopy and tandem mass spectrometry. The synthetic sample was found to be of S-configuration by VCD spectroscopy and comparison of the data with DFT calculations, while ECD spectroscopy was found to be inconclusive in this case. The enantiomeric purity of samples from test purchases and police seizures was assessed by a self-developed chiral HPLC method.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Beilstein J Org Chem Año: 2016 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Beilstein J Org Chem Año: 2016 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Alemania