JWH 412 Chemical Properties

Boiling point:

539.3±30.0 °C(Predicted)

Density 

1.14±0.1 g/cm3(Predicted)

solubility 

DMF: 20 mg/ml; DMSO: 20 mg/ml; Ethanol: 5 mg/ml

form 

A crystalline solid

JWH 412 Usage And Synthesis

Description

JWH 412 is a positional isomer of AM2201 that was identified in the ‘herbal mixture’ XoXo. The substitution of hydrogen against fluorine in the 4-position of the naphthyl moiety enhances the binding affinity to the central cannabinoid (CB₁) receptor compared to the unsubstituted JWH 018. JWH 412 demonstrates K_i values of 7.2 and 3.2 nM at CB₁ and peripheral CB₂ receptors, respectively. This product is intended for research and forensic purposes.

Uses

JWH 412 is a naphthoylindoles acting on cannabinoid receptors identified based on their fragmentation patterns under ESI-QTOFMS.

Uses

JWH 412 is a positional isomer of AM2201 that was identified in the ‘herbal mixture’ XoXo. The substitution of hydrogen against fluorine in the 4-position of the naphthyl moiety enhances the binding affinity to the central cannabinoid (CB1) receptor compared to the unsubstituted JWH 018. JWH 412 demonstrates Ki values of 7.2 and 3.2 nM at CB1 and peripheral CB2 receptors, respectively. This product is intended for research and forensic purposes.[Cayman Chemical]

References

[1] BJOERN MOOSMANN . Separation and structural characterization of the synthetic cannabinoids JWH-412 and 1-[(5-fluoropentyl)-1H-indol-3yl]-(4-methylnaphthalen-1-yl)methanone using GC–MS, NMR analysis and a flash chromatography system[J]. Forensic science international, 2012, 220 1: Pages e17-e22. DOI: 10.1016/j.forsciint.2011.12.010
[2] JENNY L. WILEY . Synthesis and pharmacology of 1-alkyl-3-(1-naphthoyl)indoles: Steric and electronic effects of 4- and 8-halogenated naphthoyl substituents[J]. Bioorganic & Medicinal Chemistry, 2012, 20 6: Pages 2067-2081. DOI: 10.1016/j.bmc.2012.01.038