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1427325-61-8

1427325-61-8 Structure

1427325-61-8 Structure
IdentificationBack Directory
[Name]

JWH 073 2-methylnaphthyl analog
[CAS]

1427325-61-8
[Synonyms]

JWH 073 2-methylnaphthyl analog
JWH-073 methylderivate (2-methylnaphthalene)
(1-butylindol-3-yl)-(2-methylnaphthalen-1-yl)methanone
[Molecular Formula]

C24H23NO
[MDL Number]

MFCD29036944
[MOL File]

1427325-61-8.mol
[Molecular Weight]

341.45
Chemical PropertiesBack Directory
[solubility ]

DMF: 20 mg/ml; DMSO: 10 mg/ml; Ethanol: 20 mg/ml; Methanol: 30 mg/ml
Safety DataBack Directory
[Symbol(GHS) ]


GHS02,GHS06,GHS08
[Signal word ]

Danger
[Hazard statements ]

H225-H301+H311+H331-H370
[Precautionary statements ]

P210-P240-P241-P242-P243-P260-P264-P270-P271-P280-P301+P310-P321-P330-P303+P361+P353-P304+P340-P307+P311-P312-P361+P364-P370+P378-P403+P233-P403+P235-P405-P501
Hazard InformationBack Directory
[Description]

JWH 073 is a synthetic cannabinoid (CB) that activates both the CB1 and the CB2 receptor (Ki = 8.9 and 38 nM, respectively).1 This cannabimimetic compound has been identified in herbal blends.2,3,4 JWH 073 2-methylnaphthyl analog differs structurally from JWH 073 by having a methyl group added at the 2 position of the naphthyl moiety. The biological and toxicological properties of this compound have not been characterized. This compound is intended for forensic and research purposes.
[References]

1. Aung, M.M., Griffin, G., Huffman, J.W., et al. Influence of the N-1 alkyl chain length of cannabimimetic indoles upon CB1 and CB2 receptor binding Drug Alcohol Depend. 60(2),133-140(2000).
2. Kikura-Hanajiri, R., Uchiyama, N., and Goda, Y. Survey of current trends in the abuse of psychotropic substances and plants in Japan Leg. Med. (Tokyo) 13(3),109-115(2011).
3. Lindigkeit, R., Boehme, A., Eiserloh, I., et al. Spice: A never ending story? Forensic Sci. Int. 191(1-3),58-63(2009).
4. Uchiyama, N., Kikura-Hanajiri, R., Ogata, J., et al. Chemical analysis of synthetic cannabinoids as designer drugs in herbal products Forensic Sci. Int. 198,31-38(2010).
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