109555-87-5
- Product Name：3-(1-Naphthoyl)indole
- Molecular Formula：C19H13NO
- Purity：99%
- Molecular Weight：271.318
Product Details;
CasNo： 109555-87-5
Molecular Formula： C19H13NO
Appearance： Pale pink solid
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1.What is the 3-(1-Naphthoyl)indole ?
3-(1-naphthoyl) indole is one of the raw materials that synthesizes a synthetic cannabinoid such as 1-pentyl-3-(1-naphthoyl) indole (JWH-018) and 1-butyl-3-(1-naphthoyl) indole (JWH-073).
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- 120-72-9
indole
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- 879-18-5
naphthalene-1-carbonic acid chloride
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- 109555-87-5
(1H-indol-3-yl)(naphthalene-1-yl)methanone
| Conditions | Yield |
|---|---|
|
With diethylaluminium chloride; In toluene; at 0 - 20 ℃; for 24h;
|
93% |
|
indole; With methylmagnesium bromide; In diethyl ether; at 20 ℃; for 2h; Inert atmosphere;
naphthalene-1-carbonic acid chloride; In diethyl ether; at 0 - 20 ℃; for 2h;
With ammonium chloride; In diethyl ether; at 20 ℃;
|
91% |
|
indole; With diethylaluminium chloride; In dichloromethane; toluene; at 0 ℃; for 0.5h;
naphthalene-1-carbonic acid chloride; In dichloromethane; toluene; at 0 ℃; for 16h;
|
70% |
|
With zirconium(IV) chloride; In 1,2-dichloro-ethane; at 30 ℃; for 20h; Inert atmosphere;
|
64% |
|
With MeMgX; In diethyl ether;
|
|
|
With methylmagnesium bromide; ammonium chloride;
|
|
|
With aluminum oxide; In neat (no solvent); at 100 ℃; for 0.133333h; Microwave irradiation; Green chemistry;
|
|
|
With methylmagnesium bromide; ammonium chloride;
|
|
|
indole; With ethylmagnesium bromide; In diethyl ether; at 0 - 20 ℃; for 0.5h;
naphthalene-1-carbonic acid chloride; In diethyl ether; at 20 ℃; for 1.5h;
|
0.25 g |
-
- 120-72-9
indole
-
- 2122-70-5
ethyl 2-(1-naphthyl)acetate
-
- 109555-87-5
(1H-indol-3-yl)(naphthalene-1-yl)methanone
| Conditions | Yield |
|---|---|
|
With potassium tert-butylate; copper diacetate; dimethyl sulfoxide; at 110 ℃; for 24h; regioselective reaction;
|
67% |
2.What is the CAS number for 3-(1-Naphthoyl)indole ?
The CAS number of 3-(1-Naphthoyl)indole is 109555-87-5.
More information of 3-(1-Naphthoyl)indole 109555-87-5 are:
|
CAS Number |
109555-87-5 |
|
Density |
1.267 g/cm3 |
|
Melting Point |
236 °C |
|
Boiling Point |
512.233 °C at 760 mmHg |
|
Flash Point |
263.978 °C |
|
Vapor Pressure |
0mmHg at 25°C |
|
Refractive Index |
1.738 |
|
HS CODE |
2933990090 |
|
PSA |
32.86000 |
|
LogP |
4.55210 |
|
Pka |
15.22±0.30(Predicted) |
3.What are another words for 3-(1-Naphthoyl)indole ?
Synonyms for 3-(1-Naphthoyl)indole 109555-87-5:Ketone,indol-3-yl 1-naphthyl (6CI);3-(1-Naphthoyl)indole;
4.What is the molecular formula of 3-(1-Naphthoyl)indole?
The chemical formula of 3-(1-Naphthoyl)indole is C19H13NO which containing 19 Carbon atoms,13 Hydrogen atoms,1 Nitrogen atoms and 1 Oxygen atoms,and the molecular weight of 3-(1-Naphthoyl)indole is 271.318.
5.What is 3-(1-Naphthoyl)indole (109555-87-5) used for?
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. Sixty to 100 nanomole per liter of 3-(1-naphthoyl) indole derivatives, such as 1-methyl-3-(1-naphthoyl) indole, 1-ethyl-3-(1-naphthoyl) indole, and 1-octyl-3-(1-naphthoyl) indole, can be detected using both of the obtained MAbs. A new alpaca VHH antibody library against 3-(1-naphthoyl)-indole derivatives was developed from alpaca immunized with 7-(3-(1-naphthoyl)-1H-indol-1-yl)-heptanoic acid-keyhole limpet hemocyanin (Hep-KLH) protein conjugates as the immunogen. From this library, two 3-(1-naphthoyl)-indole derivative-specific clones, named NN01 and NN02, were isolated using biopanning technology.
InChI:InChI=1/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
Relevant articles related to 3-(1-Naphthoyl)indole:
|
Article |
Source |
| Synthesis and pharmacology of 1-alkyl-3-(1-naphthoyl)indoles: Steric and electronic effects of 4- and 8-halogenated naphthoyl substituents |
To develop SAR at both the cannabinoid CB1 and CB2 receptors for 3-(1-naphthoyl)indoles bearing moderately electron withdrawing substituents at C-4 of the naphthoyl moiety, 1-propyl and 1-pentyl-3-(4-fluoro, chloro, bromo and iodo-1-naphthoyl) derivatives were prepared… , Bioorganic & Medicinal Chemistry Volume 20, Issue 6, 15 March 2012, Pages 2067-2081 |
|
Synthesis of 3-acylindoles: via copper-mediated oxidative decarbethoxylation of ethyl arylacetates |
Jaiswal, Anjali,Sharma, Anup Kumar,Singh, Krishna Nand supporting information, p. 1623 - 1628 (2020/03/06) |
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