Deschloroetizolam

Deschloroetizolam
Clinical data
Dependence
liability		 Moderate
Routes of
administration		 Oral, sublingual, rectal
Legal status
Legal status
  • Illegal in Sweden
Identifiers
CAS Number
PubChem CID
ChemSpider
UNII
Chemical and physical data
Formula C17H16N4S
Molar mass 308.40 g/mol
3D model (JSmol)

Deschloroetizolam (also known as Etizolam-2) is a thienotriazolodiazepine that is the dechlorinated analog of the closely related etizolam.[1][2][3] The compound has been sold as a designer drug.[4][5][6]

Deschloroetizolam is classified and controlled as a hazardous substance in Sweden as of on October 15, 2015.[7]

See also

References

  1. ↑ Karl-Heinz Weber; Adolf Bauer; Adolf Langbein; Helmut Daniel (September 1978). "Heteroaromaten mit anellierten Siebenringen, III. Umwandlung von Thienotriazolooxazepinen in Diazepine". Justus Liebigs Annalen der Chemie (in German). 1978 (8): 1257–1265. doi:10.1002/jlac.197819780806.
  2. ↑ "Patent US 3904641 - Triazolothienodiazepine compounds". Michio Nakanishi, Tetsuya Tahara, Kazuhiko Araki, Masami Shiroki. 9 September 1975. Retrieved 13 September 2015.
  3. ↑ "Patent EP 0776892 - Thienylazole compound and thienotriazolodiazepine compound". Yoshitomi Pharmaceutical Industries, Ltd. 4 June 1997. Retrieved 13 September 2015.
  4. ↑ "Deschloroetizolam". New Synthetic Drugs Database.
  5. ↑ Madeleine Pettersson Bergstrand; Anders Helander; Therese Hansson; Olof Beck (2016). "Detectability of designer benzodiazepines in CEDIA, EMIT II Plus, HEIA, and KIMS II immunochemical screening assays". Drug Testing and Analysis. doi:10.1002/dta.2003. PMID 27366870.
  6. ↑ Manchester, Kieran R.; Maskell, Peter D.; Waters, Laura (2018). "Experimental versus theoretical log D7.4, pKa and plasma protein binding values for benzodiazepines appearing as new psychoactive substances". Drug Testing and Analysis. doi:10.1002/dta.2387. ISSN 1942-7611. PMID 29582576.
  7. ↑ "Nya substanser klassas som narkotika eller hälsofarlig vara" (in Swedish). Folkhälsomyndigheten. 18 August 2015.


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