Cannabinoids

Applications 4-Nitro-benzeneethanol is a useful synthetic intermediate. It can be used to synthesize N-phenylethylindole carboxamides as SAR study of allosteric modulators of CB1 receptor. It can also be used to prepare 2-aza-2'-deoxyinosine-containing oligodeoxyribonucleotide duplexes.
References Piscitelli, F., et al.: J. Med. Chem., 55, 5627 (2012); Acedo, M., et al.: J. Org. Chem., 60, 6262 (1995)

Applications Used in the preparation of CB1 cannabinoid receptor agonists and brain imaging agents.
References Deng, H. et al; J. Med. Chem. 48, 6386 (2005)

Applications An intermediate of synergistic pesticide Boscalid. Also, used in the preparation of thieno[2.3-b]pyrrole derivatives as cannabinoid receptor agonists useful in mono- and combination therapy of diseases.
References Granger, D., et al.: Arthritis Rheum., 37, 1053 (1994), Robinson, R., et al.: J. Med. Chem., 39, 10 (1996),

Applications Used in the preparation of cannabinoids and their indole analogs with CB2 cannabinoid receptor selectivity.

Applications 1-(3,5-Bis(benzyloxy)phenyl)pentan-2-ol is an intermediate for the synthesis of 2''-Hydroxycannabidiol (H824820), which is a metabolite of Canabidiol (C175300), a major constituents in marijuana. 2''-Hydroxycannabidiol can be used to investigate canabidiol metabolism and human liver microsomes that metabolize Canabidiol into 6α-Hydroxycannabidiol.
References Jiang, R., et al.: Life Sci. 89, 165 (2011); Lander, N., et al.: Science 169, 611 (1970)

Applications N-(4-Bromopheneethyl-phthalimide is a building block used in the preparation of N-phenylethylindole carboxamides for structure activity relationship study of allosteric modulators of CB1 receptor.
References Piscitelli, F., et al.: J. Med. Chem., 55, 5627 (2012);

Applications A potent cannabinergic indole analogues as radioiodinatable brain imaging agents for the CB1 cannabinoid receptor. (AM2233) had a very high affinity for the rat CB1 receptor, with most of the affinity residing with the (R)-enantiomer.Synthetic Cannabinoids
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Neumeyer, J., et al.: J. Med. Chem., 33, 521 (1990), D'Ambra, T., et al.: Bioorg. Med. Chem. Lett., 6, 17 (1996), Schatz, A., et al.: Toxicol. Appl. Pharmacol., 142, 278 (1997),

Applications (S)-2-Benzylaziridine is a reagent for the synthesis of renin inhibitors, taurine and cannabinoid type 2 (CB2) receptor agonists.
References Kaltenbronn, J. S., et al.: J. Med. Chem 33, 838 (1990); Hu, L., et al.: J. Org. Chem. 72, 4543 (2007); Matsushima, Y., et al.: Jpn. Kokai Tokkyo Koho  JP 2012072067 A 20120412 (2012)

Applications (E)-5-(3,5-Bis(benzyloxy)phenyl)pent-4-en-2-ol is an intermediate used in the synthesis of 4''-Hydroxycannabidiol (H824830), which is a metabolite of Canabidiol (C175300), a major constituents in marijuana. 4''-Hydroxycannabidiol be used to investigate canabidiol metabolism and human liver microsomes that metabolize Canabidiol into 6α-Hydroxycannabidiol.
References Jiang, R., et al.: Life Sci. 89, 165 (2011); Lander, N., et al.: Science 169, 611 (1970)

Applications N-Boc-4-aminophenethylamine is used in the preparation of N-phenylethylindole carboxamides as SAR study of allosteric modulators of CB1 receptors.
References Piscitelli, F., et al.: J. Med. Chem., 55, 5627 (2012)

Applications Labelled AM-2233 (A575850). A potent cannabinergic indole analogues as radioiodinatable brain imaging agents for the CB1 cannabinoid receptor. (AM2233) had a very high affinity for the rat CB1 receptor, with most of the affinity residing with the (R)-enantiomer.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Neumeyer, J., et al.: J. Med. Chem., 33, 521 (1990), D'Ambra, T., et al.: Bioorg. Med. Chem. Lett., 6, 17 (1996), Schatz, A., et al.: Toxicol. Appl. Pharmacol., 142, 278 (1997),

Applications The labelled analogue of a synthetic cannabimimetic indole derivative which acts as a potent and selective agonist for the cannabinoid receptor CB1.
References Willis P.G. et al.: J. Lab. Cpd. Radiopharmac., 46, 799 (2003);

Applications A synthetic cannabimimetic indole derivative which acts as a potent and selective agonist for the cannabinoid receptor CB1. Synthetic cannabinoids
References Willis P.G. et al.: J. Lab. Cpd. Radiopharmac., 46, 799 (2003);

Applications 1-(5-Fluoropentyl)-N-tricyclo[3.3.1.13,7]dec-1-yl-1H-indazole-3-carboxamide is a derivative made in the synthesis of fluorescent heterocyclic aminoadamantanes as multifunctional neuroprotective agents. Synthetic cannabinoids
References Jacques, J., et al.: Bioorg. Med. Chem., 19, 3935 (2011);

Stability Hygroscopic
Applications (2,4-difluorophenyl)hydrazine is a reactant in the preparation of 1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalen-4-carboxamides as potent and selective CB2 receptor agonists.
References Han, S., et. al.: Bioorg. Med. Chem. Lett., 25, 322 (2015)

Applications 3-Methoxy Acetaminophen-d3 is deuterium labeled 3-Methoxy Acetaminophen (M226050). 3-Methoxy Acetaminophen is a metabolite of Acetaminophen (A161220), an analgesic and antipyretic agent used as a pain reliever to treat headache, muscle aches, and arthritis (1,2,3).
References (1) McGill, M. R. and Jaeschke, H. Pharm Res. 30, 2174 (2013)(2) Fairbrother, J.E., et al.: Anal. Profiles Drug Subs., 3, 1 (1974) (3) Hinson, J.A., et al.: Rev. Biochem. Toxicol., 2, 103 (1980)