ChemicalBook--->CAS DataBase List--->474799-41-2

474799-41-2

474799-41-2 Structure

474799-41-2 Structure
IdentificationBack Directory
[Name]

6-Nitrooxidole
[CAS]

474799-41-2
[Synonyms]

6-Nitrooxidole
6-nitroindolone
6-Nitrooxindole
6-nitroindolin-2-one
6-nitro-1,3-dihydro-2H-indol-2-one
6-nitro-2,3-dihydro-1H-indol-2-one
1,3-Dihydro-6-nitro-2H-indol-2-one
2H-Indol-2-one, 1,3-dihydro-6-nitro-
6-Nitro-2-oxindole in stock Factory
[Molecular Formula]

C8H6N2O3
[MDL Number]

MFCD09835636
[MOL File]

474799-41-2.mol
[Molecular Weight]

178.14
Chemical PropertiesBack Directory
[Boiling point ]

390.6±42.0 °C(Predicted)
[density ]

1.449
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

12.75±0.20(Predicted)
[Appearance]

Yellow to brown Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

6-Nitrooxidole(474799-41-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

3,3-bis(methoxycarbonyl)-6-nitroindolin-2-one

185433-47-0

6-Nitrooxidole

474799-41-2

The general procedure for the synthesis of 6-nitroindolin-2-one from the compound (CAS:185433-47-0) is as follows: dissolve Z 3 (5.30 g, 10 mmol) in a mixed solvent of methanol (10 mL) and 2N sodium hydroxide solution (10 mL), and the reaction was stirred at 80 °C for 30 min. Upon completion of the reaction, the reaction mixture was acidified to acidity with 1N hydrochloric acid and precipitate was precipitated. The precipitate was collected by filtration and the precipitate was stirred in boiling acetic acid (10 mL) for 1 hour. Subsequently, the mixture was cooled to room temperature and the precipitate was isolated by filtration and washed with distilled water. The final product, 6-nitroindolin-2-one, was obtained in a yield of 2.18 g in 68%.

[References]

[1] Journal of Medicinal Chemistry, 2009, vol. 52, # 14, p. 4466 - 4480
[2] Patent: WO2008/152013, 2008, A1. Location in patent: Page/Page column 16
[3] Patent: WO2008/152014, 2008, A2. Location in patent: Page/Page column 16
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