| Identification | Back Directory | [Name]
9-[1,1'-Biphenyl-4-yl]-3-bromo-9H-carbazole | [CAS]
894791-46-9 | [Synonyms]
4-BBPC
9-(4-biphenyl)-3-bromocarbazole
9-(4-Biphenylyl)-3-bromocarbazole
3-Bromo-9-(4-biphenylyl)carbazole
9-Biphenyl-3-yl-3-broMo-9H-carbazole
-Biphenyl-4-yl]-3-bromo-9H-carbazole
9-Biphenyl-2-yl-3-broMo-9H-carbazole
9-(4-Biphenylyl)-3-bromocarbazole >
3-bromo-9-(biphenyl-4-yl)-9H-carbazole
9-(biphenyl-4-yl)-3-bromo-9H-carbazole
3-Bromo-9-([1,1'-biphenyl]-4-yl)carbazole
9-([1,1'-Biphenyl]-4-yl)-3-bromo carbazole
9-[1,1'-Biphenyl-4-yl]-3-bromo-9H-carbazole
9H-Carbazole,9-[1,1'-biphenyl]-4-yl-3-bromo
9-Biphenyl-4-yl-3-broMo-9H-carbazole
(3BBPC)
9-[1,1'-Biphenyl-4-yl]-3-bromo-9H-carbazole
9-[1,1'-Biphenyl-4-yl]-3-bromo-9H-carbazole ISO 9001：2015 REACH
9H-Carbazole, 9-[1,1'-biphenyl]-4-yl-3-broMo-
3-BroMo-9-(4-biphenylyl)carbazole | [Molecular Formula]
C24H16BrN | [MDL Number]
MFCD16038226 | [MOL File]
894791-46-9.mol | [Molecular Weight]
398.29 |
| Chemical Properties | Back Directory | [Melting point ]
153.0 to 157.0 °C | [Boiling point ]
552.0±42.0 °C(Predicted) | [density ]
1.32 | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
soluble in Toluene | [form ]
powder to crystal | [color ]
White to Light yellow | [InChI]
InChI=1S/C24H16BrN/c25-19-12-15-24-22(16-19)21-8-4-5-9-23(21)26(24)20-13-10-18(11-14-20)17-6-2-1-3-7-17/h1-16H | [InChIKey]
MOCNGNGLTRMQQH-UHFFFAOYSA-N | [SMILES]
N1(C2=CC=C(C3=CC=CC=C3)C=C2)C2=C(C=CC=C2)C2=C1C=CC(Br)=C2 |
| Questions And Answer | Back Directory | [Uses]
9-[1,1'-biphenyl-4-yl]-3-bromo-9H-carbazole is widely used as an intermediate in pharmaceuticals, materials, chemical reagents, and fine chemicals. |
| Hazard Information | Back Directory | [Chemical Properties]
White crystalline powder | [Synthesis]
General procedure for the synthesis of 9-[1,1'-biphenyl-4-yl]-3-bromo-9H-carbazole from 9-(4-biphenylyl)carbazole: 3.1 g (10 mmol) of 9-(4-biphenylyl)carbazole was dissolved in 100 mL of chloroform, followed by the slow addition of 1.8 g (10 mmol) of N-bromosuccinimide. The reaction mixture was stirred at room temperature for 24 hours. Upon completion of the reaction, the organic phase was washed with water. The organic phase was dried by adding anhydrous magnesium sulfate, followed by filtration to remove the desiccant. The filtrate was concentrated to give the crude product, which was dried to obtain 3.7 g (yield: 95%) of the target compound 9-[1,1'-biphenyl-4-yl]-3-bromo-9H-carbazole as a beige powder. | [References]
[1] Patent: WO2006/70912, 2006, A1. Location in patent: Page/Page column 71; 72
[2] Patent: WO2009/72587, 2009, A1. Location in patent: Page/Page column 213-214
[3] Inorganica Chimica Acta, 2012, vol. 390, p. 119 - 122
[4] Patent: JP2015/218136, 2015, A. Location in patent: Paragraph 0064; 0070 |
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