Identification | Back Directory | [Name]
10-Bromo-7H-benzo[c]carbazole | [CAS]
1698-16-4 | [Synonyms]
1698-16-4 10-Bromo-7H-benzo[c]carbazole 10-Bromo-7H-benzo[c]carbazole1 7H-Benzo[c]carbazole, 10-bromo- 10-Bromo-7H-benzo[c]carbazole > 10-BroMo-7H-benzo[c]carbazole(10-BBC) 10-Bromo-7H-benzo[c]carbazole | [Molecular Formula]
C16H10BrN | [MDL Number]
MFCD22054961 | [MOL File]
1698-16-4.mol | [Molecular Weight]
296.17 |
Chemical Properties | Back Directory | [Melting point ]
131-133℃ | [Boiling point ]
502.8±23.0 °C(Predicted) | [density ]
1.589 | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [form ]
powder to crystal | [pka]
16.41±0.30(Predicted) | [color ]
White to Light gray to Light yellow | [InChI]
InChI=1S/C16H10BrN/c17-11-6-8-14-13(9-11)16-12-4-2-1-3-10(12)5-7-15(16)18-14/h1-9,18H | [InChIKey]
YHAHNQXQOZYZLP-UHFFFAOYSA-N | [SMILES]
N1C2=C(C=C(Br)C=C2)C2=C1C=CC1=CC=CC=C12 |
Hazard Information | Back Directory | [Uses]
10-Bromo-7H-benzo[c]carbazole is an electroluminescent material. | [Synthesis]
The 20.4g (0.1mol) 7H- benzo [c] carbazole was dissolved in tetrahydrofuran (THF, 500mL), and then the resulting solution was stirred at 0 10 minutes. Thereto was added N- bromosuccinimide (NBS, 18.68g, 0.105mol), the resulting mixture was stirred at normal temperature for 12 hours, then extracted with ethyl acetate and distilled water. The organic layer was dried over anhydrous magnesium sulfate (MgSO4) was dried, and then the solvent was removed and subjected to silica gel column chromatography to give 25.4g (86percent) 10-Bromo-7H-benzo[c]carbazole.
| [References]
[1] Patent: WO2013/32297, 2013, A1. Location in patent: Paragraph 147; 148 [2] Patent: CN105601621, 2016, A. Location in patent: Paragraph 0297; 0298; 0299 [3] Patent: WO2013/73874, 2013, A1. Location in patent: Paragraph 166; 167 [4] Patent: WO2012/36482, 2012, A1. Location in patent: Page/Page column 33 [5] Patent: JP2015/189722, 2015, A. Location in patent: Paragraph 0145; 0148 |
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