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654676-12-7

654676-12-7 Structure

654676-12-7 Structure
IdentificationBack Directory
[Name]

2,7-Dibromo-9-hexylcarbazole
[CAS]

654676-12-7
[Synonyms]

2,7-Dibromo-9-hexylcarbazole
2,7-dibromo-9-hexyl-9H-carbazole
9H-Carbazole, 2,7-dibromo-9-hexyl
2,7-Dibromo-9-hexylcarbazole ISO 9001:2015 REACH
[Molecular Formula]

C18H19Br2N
[MDL Number]

MFCD29089359
[MOL File]

654676-12-7.mol
[Molecular Weight]

409.16
Chemical PropertiesBack Directory
[Melting point ]

72.0 to 76.0 °C
[Boiling point ]

486.3±38.0 °C(Predicted)
[density ]

1.50±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

soluble in Toluene
[form ]

powder to crystal
[color ]

White to Light yellow
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933.99.8290
Spectrum DetailBack Directory
[Spectrum Detail]

2,7-Dibromo-9-hexylcarbazole(654676-12-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

1-Bromohexane

111-25-1

2,7-DIBROMO-9H-CARBAZOLE

136630-39-2

2,7-Dibromo-9-hexylcarbazole

654676-12-7

General procedure for the synthesis of 2,7-dibromo-9-ethyl-9H-carbazole from bromohexane and 2,7-dibromocarbazole: A mixture of 2,7-dibromo-9H-carbazole (10 mmol), ethidium bromide (10.5 mmol), benzyltriethylammonium chloride (0.227 g, 1 mmol), toluene (20 mL), and a 50% w/v aqueous sodium hydroxide (0.42 g 10.5 mmol) The mixture was stirred at 80 °C for 14 hours. Upon completion of the reaction, the mixture was cooled to room temperature, poured into 50 mL of water and acidified with 10% hydrochloric acid to pH ≈ 2. The organic layer was separated and the aqueous phase was further extracted with toluene (2 × 10 mL). The organic phases were combined, washed with water (2 x 25 mL), dried over anhydrous sodium sulfate, filtered and concentrated to dryness. The crude product was purified by column chromatography to afford the target compound 2,7-dibromo-9-ethyl-9H-carbazole.

[References]

[1] Dyes and Pigments, 2016, vol. 124, p. 133 - 144
[2] Patent: CN105384679, 2016, A. Location in patent: Paragraph 0009; 0025; 0026; 0027
[3] Journal of Materials Chemistry C, 2016, vol. 4, # 26, p. 6270 - 6279
[4] Heterocycles, 2010, vol. 81, # 4, p. 977 - 984
[5] Journal of Organic Chemistry, 2008, vol. 73, # 23, p. 9207 - 9213
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