ChemicalBook--->CAS DataBase List--->1143-50-6

1143-50-6

1143-50-6 Structure

1143-50-6 Structure
IdentificationBack Directory
[Name]

5H-DIBENZO(B,E)AZEPINE-6,11-DIONE
[CAS]

1143-50-6
[Synonyms]

6,11(5H)-Morphanthridinedione
5H-dibenz[b,e]azepine-6,11-dione
5H-DIBENZO(B,E)AZEPINE-6,11-DIONE
5H-benzo[c][1]benzazepine-6,11-dione
[EINECS(EC#)]

214-539-6
[Molecular Formula]

C14H9NO2
[MDL Number]

MFCD00612476
[MOL File]

1143-50-6.mol
[Molecular Weight]

223.23
Chemical PropertiesBack Directory
[Melting point ]

245-246 °C
[Boiling point ]

230-234 °C(Press: 0.3 Torr)
[density ]

1.291±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

12.43±0.20(Predicted)
[Appearance]

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

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

5H-DIBENZO(B,E)AZEPINE-6,11-DIONE(1143-50-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

Anthraquinone

84-65-1

5H-DIBENZO(B,E)AZEPINE-6,11-DIONE

1143-50-6

General procedure for the synthesis of 5H-dibenzo[b,e]azepine-6,11-dione using anthraquinone as starting material: a mixed solution of concentrated sulfuric acid (25.2 mL) and dichloromethane (DCM) (8.4 mL) was cooled to 0 °C, followed by the addition of anthraquinone (1) (5 g, 24 mmol). Sodium azide (1.84 g, 28.3 mmol) was added in small batches at 0-5 °C, taking about 1 hour. The reaction mixture was stirred overnight at room temperature and then slowly poured into ice water (300 mL). The product was collected by filtration, washed with water to neutral to remove residual acid, and dried to afford 5H-dibenzo[b,e]azepine-6,11-dione (2) as a white solid (5.3 g, 100% yield). Mass spectral data: m/z = 224 ([M + H]+).

[References]

[1] Patent: WO2007/25938, 2007, A1. Location in patent: Page/Page column 13
[2] Patent: WO2006/116157, 2006, A2. Location in patent: Page/Page column 112
[3] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 3, p. 441 - 446
[4] Journal of the Chemical Society, 1958, p. 4200
[5] Gazzetta Chimica Italiana, 1953, vol. 83, p. 533,536
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