3-Fluoropentyl<wbr/>indole

3-Fluoropentylindole

CAT N°: 15452

A wide variety of aminoalkylindole analogs are potent synthetic cannabinoids (CBs), including many of the JWH compounds.{16798} An alkyl chain of five carbons in length produces compounds with high affinity for both the central CB1 and the peripheral CB2 receptors.{16797} The addition of a terminal fluorine to the pentyl chain can further increase affinity for both CB receptors.{18696} 3-Fluoropentylindole is the base structure for various synthetic CBs that features a fluorine at the three position of the pentyl chain. A range of structures can be added to this base via a ketone linkage at the three position of the indole. The physiological and toxicological properties of this compound have not been evaluated. This product is intended for forensic and research applications.

Territorial Availability: Available through Bertin Technologies only in France

Technical Warning: Bertin Technologies restricts the sale of this product to licensed controlled substance laboratories and qualified academic research institutions. Please contact us for further details.

Special Advice: Please check regulation status before ordering; additionel fees can apply.

  • Synonyms
    • 1-(3-fluoropentyl)-1H-indole
  • Correlated keywords
    • cannabinoids forensics neurosciences fluoro pentyl indoles analytical references standards aminoalkylindole analogs CBs JWHs central CB1 peripheral CB2 receptors synthetics ketones linkages
  • Product Overview:
    A wide variety of aminoalkylindole analogs are potent synthetic cannabinoids (CBs), including many of the JWH compounds.{16798} An alkyl chain of five carbons in length produces compounds with high affinity for both the central CB1 and the peripheral CB2 receptors.{16797} The addition of a terminal fluorine to the pentyl chain can further increase affinity for both CB receptors.{18696} 3-Fluoropentylindole is the base structure for various synthetic CBs that features a fluorine at the three position of the pentyl chain. A range of structures can be added to this base via a ketone linkage at the three position of the indole. The physiological and toxicological properties of this compound have not been evaluated. This product is intended for forensic and research applications.

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