Azidoindolene 1

Azidoindolene 1

CAT N°: 17083

UR-144 (Item No. 11502) and XLR11 (Item No. 11565) are potent synthetic cannabinoids (CBs) that have been identified as adulterants of herbal products.{22648,23290} Azidoindolene 1 is structurally similar to UR-144, XLR11, and a number of additional synthetic CBs with a hydrazide linking the tetramethylcyclopropyl group to the aminoalkylindole group. The physiological and toxicological properties of this compound are not known. Typically, a tetramethylcyclopropyl group confers selectivity for the peripheral CB2 receptor, and the addition of substituents at the N1-amine of the aminoalkylindole group is necessary for high affinity at either CB1 or CB2.{20487} 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
    • 2,2,3,3-tetramethyl-cyclopropanecarboxylic acid (2Z)-2-[1-(5-fluoropentyl)-1,2-dihydro-2-oxo-3H-indol-3-ylidene]hydrazide
  • Correlated keywords
    • cannabinoid cannabimimetic CB2 CB1 forensic UR-144 XLR11 science biochemical UR144 XLR-11 synthetic CB adulterant herbal product structurally similar hydrazide linking tetramethylcyclopropyl group aminoalkylindole selectively peripheral receptor addition substituent N1-amine research application analytical reference standard
  • Product Overview:
    UR-144 (Item No. 11502) and XLR11 (Item No. 11565) are potent synthetic cannabinoids (CBs) that have been identified as adulterants of herbal products.{22648,23290} Azidoindolene 1 is structurally similar to UR-144, XLR11, and a number of additional synthetic CBs with a hydrazide linking the tetramethylcyclopropyl group to the aminoalkylindole group. The physiological and toxicological properties of this compound are not known. Typically, a tetramethylcyclopropyl group confers selectivity for the peripheral CB2 receptor, and the addition of substituents at the N1-amine of the aminoalkylindole group is necessary for high affinity at either CB1 or CB2.{20487} This product is intended for forensic and research applications.

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