(4-ethylnaphthalen-1-yl)-[1-(5-hydroxypentyl)indol-3-yl]methanone

(4-ethylnaphthalen-1-yl)-[1-(5-hydroxypentyl)indol-3-yl]methanone Suppliers list
Company Name: Shanghai Hongye Biotechnology Co. Ltd  
Tel: 400-9205774 400-920-5774
Email: sales@glpbio.cn
Company Name: ChemeGen(Shanghai) Biotechnology Co.,Ltd.  
Tel: 18818260767
Email: sales@chemegen.com
Company Name: Energy Chemical  
Tel: 021-58432009 400-005-6266
Email: marketing@energy-chemical.com
(4-ethylnaphthalen-1-yl)-[1-(5-hydroxypentyl)indol-3-yl]methanone Basic information
Product Name:(4-ethylnaphthalen-1-yl)-[1-(5-hydroxypentyl)indol-3-yl]methanone
Synonyms:(4-ethylnaphthalen-1-yl)-[1-(5-hydroxypentyl)indol-3-yl]methanone;Methanone, (4-ethyl-1-naphthalenyl)[1-(5-hydroxypentyl)-1H-indol-3-yl]-
CAS:1427521-40-1
MF:C26H27NO2
MW:385.5
EINECS:
Product Categories:
Mol File:1427521-40-1.mol
(4-ethylnaphthalen-1-yl)-[1-(5-hydroxypentyl)indol-3-yl]methanone Structure
(4-ethylnaphthalen-1-yl)-[1-(5-hydroxypentyl)indol-3-yl]methanone Chemical Properties
Boiling point 606.6±45.0 °C(Predicted)
density 1.12±0.1 g/cm3(Predicted)
solubility DMF: 15 mg/ml; DMSO: 14 mg/ml; Ethanol: 15 mg/ml
form A crystalline solid
pka15.17±0.10(Predicted)
Safety Information
MSDS Information
(4-ethylnaphthalen-1-yl)-[1-(5-hydroxypentyl)indol-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-carboxypentyl metabolites detected in the urine.1,2,3 JWH 210 N-(5-hydroxypentyl) metabolite is an expected metabolite of JWH 210, detectable in the serum and urine. Its biological activities have yet to be determined. This product is intended for forensic purposes.
UsesJWH-210 (Indole-d5) 5-Hydroxypentyl JWH-210 5-Hydroxypentyl (J211490) which is a urinary metabolite of JWH-210, an analgesic chemical that acts as a potent cannabinoid agonist at both the CB1 and CB2 receptors.
References1. Teske, J., Weller, J.P., Fieguth, A., et al. 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. Chromatogr. B Analyt. Technol. Biomed. Life Sci. 878(27),2659-2663(2010).
2. Sobolevsky, T., Prasolov, I., and Rodchenkov, G. Detection of JWH-018 metabolites in smoking mixture post-administration urine Forensic Sci. Int. 200(1-3),141-147(2010).
3. Wintermeyer, A., Mller, I., Thevis, M., et al. In vitro phase I metabolism of the synthetic cannabimimetic JWH-018 Anal. Bioanal. Chem. 398(5),2141-2153(2010).
(4-ethylnaphthalen-1-yl)-[1-(5-hydroxypentyl)indol-3-yl]methanone Preparation Products And Raw materials
Tag:(4-ethylnaphthalen-1-yl)-[1-(5-hydroxypentyl)indol-3-yl]methanone(1427521-40-1) Related Product Information
JWH 203 N-(4-hydroxypentyl) metabolite JWH 203 N-(5-hydroxypentyl) metabolite JWH 398 N-(4-hydroxypentyl) metabolite 1-[1-(5-hydroxypentyl)indol-3-yl]-2-(2-methoxyphenyl)ethanone JWH 250 N-(4-hydroxypentyl) metabolite