(4-ethylnaphthalen-1-yl)-(5-hydroxy-1-pentylindol-3-yl)methanone

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(4-ethylnaphthalen-1-yl)-(5-hydroxy-1-pentylindol-3-yl)methanone Basic information
Product Name:(4-ethylnaphthalen-1-yl)-(5-hydroxy-1-pentylindol-3-yl)methanone
Synonyms:(4-ethylnaphthalen-1-yl)-(5-hydroxy-1-pentylindol-3-yl)methanone;JWH-210 5-hydroxyindole;(4-ethylnaphthalen-1-yl)(5-hydroxy-1-pentyl-1H-indol-3-yl)methanone;Methanone, (4-ethyl-1-naphthalenyl)(5-hydroxy-1-pentyl-1H-indol-3-yl)-
CAS:1427325-81-2
MF:C26H27NO2
MW:385.5
EINECS:
Product Categories:
Mol File:1427325-81-2.mol
(4-ethylnaphthalen-1-yl)-(5-hydroxy-1-pentylindol-3-yl)methanone Structure
(4-ethylnaphthalen-1-yl)-(5-hydroxy-1-pentylindol-3-yl)methanone Chemical Properties
Boiling point 601.8±45.0 °C(Predicted)
density 1.13±0.1 g/cm3(Predicted)
solubility DMF: 20 mg/ml; DMSO: 20 mg/ml
form A crystalline solid
pka9.41±0.40(Predicted)
Safety Information
MSDS Information
(4-ethylnaphthalen-1-yl)-(5-hydroxy-1-pentylindol-3-yl)methanone Usage And Synthesis
DescriptionJWH 210 is a potent cannabimimetic alkylindole that has been identified in extracts from herbal blends. Structurally and functionally similar alkylindoles are rapidly metabolized by the liver and secreted in the urine, with 5-hydroxyindole metabolites detected both in liver secretions and in urine. JWH 210 5-hydroxyindole metabolite is an expected metabolite of JWH 210, detectable both in serum and urine. Its biological activities have yet to be determined.
References[1] JRG TESKE. Sensitive and rapid quantification of the cannabinoid receptor agonist naphthalen-1-yl-(1-pentylindol-3-yl)methanone (JWH-018) in human serum by liquid chromatography-tandem mass spectrometry.[J]. Journal of Chromatography B, 2010, 878 27: 2659-2663. DOI: 10.1016/j.jchromb.2010.03.016
(4-ethylnaphthalen-1-yl)-(5-hydroxy-1-pentylindol-3-yl)methanone Preparation Products And Raw materials
Tag:(4-ethylnaphthalen-1-yl)-(5-hydroxy-1-pentylindol-3-yl)methanone(1427325-81-2) Related Product Information
JWH 018 5-hydroxyindole metabolite JWH 073 6-hydroxyindole metabolite (6-hydroxy-1-pentylindol-3-yl)-naphthalen-1-ylmethanone (1-butyl-4-hydroxyindol-3-yl)-naphthalen-1-ylmethanone JWH 018 7-hydroxyindole metabolite