| Identification | Back Directory | [Name]
JWH 398 | [CAS]
1292765-18-4 | [Synonyms]
JWH 398
JWH 398 (exempt preparation)
(4-chloronaphthalen-1-yl)-(1-pentylindol-3-yl)methanone
(4-Chloro-1-naphthalenyl)(1-pentyl-1H-indol-3-yl)Methanone
(4-chloronaphthalen-1-yl)(1-pentyl-1H-indol-3-yl)Methanone
Methanone, (4-chloro-1-naphthalenyl)(1-pentyl-1H-indol-3-yl)- | [Molecular Formula]
C24H22ClNO | [MDL Number]
MFCD27966837 | [MOL File]
1292765-18-4.mol | [Molecular Weight]
375.89 |
| Chemical Properties | Back Directory | [Boiling point ]
561.7±30.0 °C(Predicted) | [density ]
1.17±0.1 g/cm3(Predicted) | [solubility ]
DMF: 5 mg/ml; DMSO: 5 mg/ml; Ethanol: 30 mg/ml; Methanol: 5 mg/ml |
| Hazard Information | Back Directory | [Description]
JWH 398 (exempt preparation) (Item No. 15686) is an analytical reference standard categorized as a synthetic cannabinoid. JWH 398 is regulated as a Schedule I compound in the United States. JWH 398 (exempt preparation) (Item No. 15686) is provided as a DEA exempt preparation. This product is intended for research and forensic applications. | [Uses]
JWH-398 is a synthetic cannabimimetic indole derivative that acts as both a cannabinoid receptor CB1 and CB2 agonist. | [Definition]
ChEBI: JWH 398 is an indolecarboxamide. | [References]
[1] HUFFMAN J. Cannabimimetic Indoles, Pyrroles, and Indenes: Structure–Activity Relationships and Receptor Interactions[C]. 1900: 0. DOI: 10.1007/978-1-59745-503-9_3 |
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