Grundinformationen
- Standard-SMILES
c1ccc(-c2ccc3ccccc3n2)cc1- InChIKey
FSEXLNMNADBYJU-UHFFFAOYSA-N- Summenformel
- C15H11N
- Durchschnittliche Molmasse
- 205,25 g/mol
- Monoisotopische Masse
- 205,08914936
Namen und Bezeichner
- Bevorzugter Name
- 2-Phenylquinoline
- IUPAC
- 2-phenylquinoline
- Lokaler Name
- 2-Phenylchinolin
- Englischer Name
- 2-Phenylquinoline
- Summenformel
- C15H11N
- Molmasse
- 205.25
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
612-96-4- PubChem CID
- 71545
- DTXSID
DTXSID30210115- ChEMBL
CHEMBL89786- EC Number
- 210-326-7
- Nikkaji
- J101.652K
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 3,9
- Polarare Oberfläche (TPSA)
- 12,9 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 1
- Frei drehbare Bindungen
- 1
- Schwere Atome
- 16
- Formalladung
- 0
- Komplexität
- 219
Experimentelle und physikochemische Eigenschaften
Physikochemische Eigenschaften
- Schmelzpunkt
- 84 · 84-85 °C (lit.)
- Siedepunkt
- 363 °C · 363 °C
- Dichte
- 1.1155 · 1.1155 (rough estimate)
- Brechungsindex
- 1.655 · 1.6550 (estimate)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 4.52 · 4.52±0.10(Predicted)
- Aggregatzustand
- Crystalline Powder
- Farbe
- White to light yellow
- Wasserlöslichkeit
- SLIGHTLY SOLUBLE
- InChI
- 1S/C15H11N/c1-2-6-12(7-3-1)15-11-10-13-8-4-5-9-14(13)16-15/h1-11H
- InChIKey
- FSEXLNMNADBYJU-UHFFFAOYSA-N
- SMILES
- c1ccc(cc1)-c2ccc3ccccc3n2
- CAS Datenbank
- 612 · 612-96-4(CAS DataBase Reference)
- NIST chemische Informationen
- 2 · Quinoline, 2-phenyl-(612-96-4)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Warning
H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation];H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation];H335 (97.6%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 41 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.;Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.
Gefahrenhinweise
Sicherheitsdaten
- wgk
- 3
- hs_code
- 29334900
- risk_code
- 36/37/38
- hazard_code
- Xi
- safety_code
- 26-37/39
- Speicherklasse
- 11 - Combustible Solids
- Hazard Classifications
- Eye Irrit. 2Skin Irrit. 2STOT SE 3
Chemie und Industrie
Anwendungen
Beschreibung2-Phenylquinoline is the major quinoline alkaloid of Galipea iongiflora, a Bolivian plant used as treatment for cutaneous leishmaniasis. Antinociceptive properties of 2-phenylquinoline isolated from the bark of Galipea iongiflora against different models of pain in mice were evaluated.
Darstellung
synthetischeSynthesis of 2-phenylquinoline: Quinoline (1.0 g, 7.742 mmol) and phenyl lithium (2.30 mL, 2 M, 23.22 mmol) were reacted according to general procedure. Purification of the residue by silica gel column chromatography (EtOAc:MeOH:Et3N; 10-30:1:1 or PhMe:MeOH:Et3N; 10:1:1) gave 2-phenylquinoline (0.66 g, 42%) as an orange solid.Aniline (0.140 g, 1.50 mmol) and cinnamaldehyde (0.132 g, 1.00 mmol) were dissolved in toluene in a reaction vial equipped with a magnetic stirrer bar, followed by the addition of K10 (0.50 g). The reaction mixture was heated at a temperature of 110 C for 3 hours. After completion of the reaction, the crude product was purified by column chromatography over silica gel eluting with a mixture of Hexane : Ethyl acetate (20:1) to produce 2-Phenylquinoline as a yellow solid (0.044 g, 21%); (m.p. 82-84 C) (lit. 84-85 °C); Rf 0.67 (20:1 hexane:ethyl acetate);1H NMR (400 MHz, CDCl3) δH 7.46-7.51 (1H, m, H-4’), 7.53-7.56 (3H, m, H-6, 3’, 5’), 7.73- 7.77 (1H, m, H-7), 7.85 (1H, d, J = 8.31 Hz, H-5), 7.88-7.91 (1H, d, J = 8.31 Hz, H-3), 8.18- 8.27 (4H, m, H-4, 8, 2’, 6’)13C NMR(400 MHz, CDCl3) δC 119.2 (C-3), 126.7 (C-6), 127.2 (C-4a), 127.5 (C-2’, 6’), 127.9 (C-5), 128.4 (C-3’, 5’), 128.7 (C-4’), 128.9 (C-7, 8), 129.8 (C-4), 130.3 (C-1’), 137.9 (C-8a), 157.2 (C-2)
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