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- 9-Phenylanthracene
-
-
2026-09-20
- CAS:602-55-1
- Min. Order: 1kg
- Purity: 99.95%min
- Supply Ability: 2000kgs
- 9-phenylanthracene
-
-
2026-09-20
- CAS:602-55-1
- Min. Order: 1KG
- Purity: 98%min
- Supply Ability: 30tons/month
- 9-PHENYLANTHRACENE
-
-
2026-08-18
- CAS:602-55-1
- Min. Order: 1KG
- Purity: 98.00%
- Supply Ability: 150KG /month
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| | 9-phenylanthracene Basic information |
| | 9-phenylanthracene Chemical Properties |
| Melting point | 153-155 °C (lit.) | | Boiling point | 417 °C (lit.) | | density | 1.1180 (estimate) | | refractive index | 1.7040 (estimate) | | storage temp. | Sealed in dry,Room Temperature | | solubility | Chloroform (Slightly), Ethyl Acetate (Slightly) | | form | Solid | | color | Off-white to pale brown | | Sensitive | Light Sensitive | | BRN | 1910570 | | InChI | InChI=1S/C20H14/c1-2-8-15(9-3-1)20-18-12-6-4-10-16(18)14-17-11-5-7-13-19(17)20/h1-14H | | InChIKey | LUBXLGUQZVKOFP-UHFFFAOYSA-N | | SMILES | C1=C2C(C=C3C(=C2C2=CC=CC=C2)C=CC=C3)=CC=C1 | | CAS DataBase Reference | 602-55-1(CAS DataBase Reference) | | EPA Substance Registry System | Anthracene, 9-phenyl- (602-55-1) |
| Hazard Codes | N | | Risk Statements | 50/53 | | Safety Statements | 60-61 | | RIDADR | UN 3077 9/PG 3 | | WGK Germany | 3 | | HazardClass | 9 | | HS Code | 29029090 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Aquatic Acute 1
Aquatic Chronic 1 |
| | 9-phenylanthracene Usage And Synthesis |
| Chemical Properties | Pale Yellow Plates | | Uses | 9-Phenylanthracene is used to synthesize organic light-emitting material intermediates. | | Preparation | The synthesis of 9-phenylanthracene involved mixing phenylboronic acid (2.13 g, 17.49 mmol), 9-bromoanthracene (3 g, 11.66 mmol), Pd(PPh3)4 (140 mg, 0.12 mmol), K2CO3 (16 mL, 2 M), and ethanol (8 mL) in a 100 mL flask with anhydrous toluene (32 mL). The mixture was refluxed for 48 h under nitrogen. After cooled to room temperature, the reaction mixture was quenched with dilute hydrochloric acid solution and extracted with CH2Cl2. The organic extracts were dried over anhydrous MgSO4 and concentrated by rotary evaporation. The crude product was further purified by silica gel column chromatography (CH2Cl2/petroleum ether (1:4,v/v)) to get a white powder (2.43 g, 81.9 %). 1H NMR (500 MHz, CDCl3) δ 8.53 (s, 1H), 8.08 (d, J = 8.5 Hz, 2H), 7.70 – 7.67 (m, 2H), 7.63 – 7.54 (m, 3H), 7.50 – 7.45 (m, 4H), 7.37 (ddd, J = 8.7, 6.5, 1.2 Hz, 2H). EI-MS (m/z): Calculated for C20H14: 254.33. Found [M+]: 253.02.
Synthesis of 9-phenylanthracene | | Synthesis Reference(s) | Journal of the American Chemical Society, 79, p. 393, 1957 DOI: 10.1021/ja01559a042 | | Purification Methods | Chromatograph it on alumina in *C6H6 and recrystallise it from AcOH or toluene. [Beilstein 5 H 725, 5 II 639, 5 III 2462.] |
| | 9-phenylanthracene Preparation Products And Raw materials |
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