Тип публикации: статья из журнала

Год издания: 2015

Идентификатор DOI: 10.1016/j.forsciint.2015.08.023

Ключевые слова: Designer drugs, Cannabinoids, NMR, GC-MS, Indole-3-carboxylic acid, CBL-2201, carboxylic acid, designer drug, naphthalene, napth 1 yl (5 fluoropenty)1h indole 3 carboxylate, unclassified drug, Article, carbon nuclear magnetic resonance, drug structure, drug synthesis, infrared spectroscopy, mass fragmentography, molecular weight, nitrogen nuclear magnetic resonance, priority journal, proton nuclear magnetic resonance, structure analysis

Аннотация: The H-1, C-13 and N-15 nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy (FT-IR) and gas chromatography coupled to mass spectrometry (GC-MS) identification of a synthetic cannabinoid compound has been conducted. It was shown that this compound cannot be reliably distinguished from the closely related quinoliПоказать полностьюn-8-yl indole-3-carboxylic acid derivative by an automatic search in MS library. Structural difference of the studied compound and known illicit compounds has been determined using 1D and 2D NMR spectroscopy. Analytical data for the identification of this compound were provided. (C) 2015 Elsevier Ireland Ltd. All rights reserved.

Журнал: FORENSIC SCIENCE INTERNATIONAL

Выпуск журнала: Vol. 257

Номера страниц: 209-213

ISSN журнала: 03790738

Место издания: CLARE

Издатель: ELSEVIER IRELAND LTD

• Kondrasenko A.A. (Institute of Chemistry and Chemical Technology of the Siberian Branch of Russian Academy of Sciences)
• Goncharov E.V. (Expert and Criminalistics Branch of the Department of the FDCS of Russia in Krasnoyarsk Territory)
• Dugaev K.P. (Expert and Criminalistics Branch of the Department of the FDCS of Russia in Krasnoyarsk Territory)
• Rubaylo A.I. (Krasnoyarsk Scientific Center of the Siberian Branch of Russian Academy of Sciences)

• Web of Science Core Collection
• Scopus
• Ядро РИНЦ (eLIBRARY.RU)