3-(1-Naphthoyl)indole
- CAS No.
- 109555-87-5
- Chemical Name:
- 3-(1-Naphthoyl)indole
- Synonyms
- 3Naphthoylindole;-Naphthoyl Indole;3 Naphthoylindole;3-Naphthoylindole;1'-Naphthoyl Indole;3-(1-Naphthoyl)indole;3-(1-naphthylcarbonyl)indole;Ketone indol-3-yl 1-naphthyl;Indol-3-yl 1-Naphthyl Ketone;3- (1-Naphthoyl) Indole Powder
- CBNumber:
- CB52471302
- Molecular Formula:
- C19H13NO
- Molecular Weight:
- 271.31
- MOL File:
- 109555-87-5.mol
- MSDS File:
- SDS
- Modify Date:
- 2024/5/28 14:12:21
| Melting point | 236℃ |
|---|---|
| Boiling point | 512.2±23.0 °C(Predicted) |
| Density | 1.267 |
| storage temp. | Sealed in dry,2-8°C |
| solubility | DMSO (Slightly), Methanol (Slightly) |
| form | Solid |
| pka | 15.22±0.30(Predicted) |
| color | Pale Orange to Light Pink |
| InChI | InChI=1S/C19H13NO/c21-19(17-12-20-18-11-4-3-9-15(17)18)16-10-5-7-13-6-1-2-8-14(13)16/h1-12,20H |
| InChIKey | QIXQGVQLBPQVOR-UHFFFAOYSA-N |
| SMILES | C(C1C2=C(NC=1)C=CC=C2)(C1=C2C(C=CC=C2)=CC=C1)=O |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |  GHS07 |
|||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Signal word | Warning | |||||||||
| Hazard statements | H302 | |||||||||
| Precautionary statements | P280-P305+P351+P338 | |||||||||
| NFPA 704 |
|
3-(1-Naphthoyl)indole Chemical Properties,Uses,Production
Description
3-(1-Naphthoyl)indole is a synthetic cannabinoid that is structurally similar to THC. It has been detected in human urine, plasma and autopsy samples by high-resolution mass spectrometry. It has been found to be hydroxylated into a number of metabolites including carboxy-3-(1-naphthoyl)indole, which may account for some of the psychoactive effects.
Chemical Properties
Off-White to Light Pink Solid.
Uses
Metabolite of JWH-018 (P283650).
Synthesis
To a cooled solution of indole (5.85g, 50mmol) in ether (50ml) under nitrogen was added slowly a solution of methylmagnesium bromide (3M) in ether (17.5ml). After addition, the reaction mixture was warmed up to room temperature and stirred for 2h at room temperature. Then, the mixture was cooled down again to 0°C and added slowly, stirring a solution of 1-naphthoylchloride (9.5g, 50mmol) in ether (50ml). The resulting mixture was warmed up to room temperature and stirred for 2h at room temperature, followed by a slow addition of saturated ammonium chloride solution (375ml). The mixture was then stirred overnight at room temperature. A white solid was formed, filtered, washed by ether, and dried under a high vacuum to give 3-(1-Naphthoyl)indole (12.3g, 91%).
3-(1-Naphthoyl)indole Preparation Products And Raw materials
3-(1-Naphthoyl)indole Suppliers
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