ChemicalBook--->CAS DataBase List--->1984-49-2

1984-49-2

1984-49-2 Structure

1984-49-2 Structure
IdentificationBack Directory
[Name]

3,3'-Bicarbazole
[CAS]

1984-49-2
[Synonyms]

3,3'-CZ
3,3'-Bicarbazole
3,3'-Dicarbazole
9H-3,3'-bicarbazole
3,3'-Bicarbazole >
3,3'-Bi-9H-carbazole
9H,9H-[3,3]Bicarbazolyl
9H,9'H-3,3'-bicarbazole
9H,9'H-3,3'-Bicarbazole,>98%
3,3'-Bi-9H-carbazole (9CI, ACI)
3-(9H-carbazol-3-yl)-9H-carbazole
3,3'-Bicarbazole ISO 9001:2015 REACH
[Molecular Formula]

C24H16N2
[MDL Number]

MFCD11046470
[MOL File]

1984-49-2.mol
[Molecular Weight]

332.4
Chemical PropertiesBack Directory
[Melting point ]

365 °C
[Boiling point ]

656.0±30.0 °C(Predicted)
[density ]

1.341
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder to crystal
[pka]

16.79±0.30(Predicted)
[color ]

White to Light yellow to Dark green
[InChI]

InChI=1S/C24H16N2/c1-3-7-21-17(5-1)19-13-15(9-11-23(19)25-21)16-10-12-24-20(14-16)18-6-2-4-8-22(18)26-24/h1-14,25-26H
[InChIKey]

PUMOFXXLEABBTC-UHFFFAOYSA-N
[SMILES]

N1C2=C(C=CC=C2)C2=C1C=CC(C1=CC3C4=C(NC=3C=C1)C=CC=C4)=C2
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[Risk Statements ]

36
[Safety Statements ]

26
[WGK Germany ]

WGK 3
[HS Code ]

2933.99.8290
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Irrit. 2
Hazard InformationBack Directory
[Uses]

3,3'-bicarbazole can be used to synthesize liquid crystal materials.
[Synthesis]

Carbazole

86-74-8

3,3'-Bicarbazole

1984-49-2

The general procedure for the synthesis of 3,3'-bicarbazole from carbazole was as follows: carbazole (10 g, 59.8 mmol), ferric(III) chloride (38.8 g, 239.3 mmol), and chloroform (200 mL) were added sequentially to a 400 mL four-necked flask, and the reaction was stirred at room temperature for 30 min. Upon completion of the reaction, the organic solvent was removed by distillation under reduced pressure. The residue was washed with methanol and the solid product was collected by filtration. The methanol washing step was repeated twice to finally obtain the intermediate 3,3'-bicarbazole (16.7 g, 84% yield).

[References]

[1] Patent: TWI540129, 2016, B. Location in patent: Paragraph 0090-0092
[2] Patent: KR101802423, 2017, B1. Location in patent: Paragraph 0153 - 0156
[3] Molecules, 2018, vol. 23, # 4,
[4] Patent: JP5727237, 2015, B2. Location in patent: Paragraph 0123
[5] J. Gen. Chem. USSR (Engl. Transl.), 1992, vol. 62, # 1.2, p. 164 - 168
Spectrum DetailBack Directory
[Spectrum Detail]

3,3'-Bicarbazole(1984-49-2)1HNMR
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