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ChemicalBook--->CAS DataBase List--->30450-62-5

30450-62-5

30450-62-5 Structure

30450-62-5 Structure
IdentificationMore
[Name]

7-Nitro-1,2,3,4-tetrahydroquinoline
[CAS]

30450-62-5
[Synonyms]

1,2,3,4-TETRAHYDRO-7-NITROQUINOLINE
7-NITRO-1,2,3,4-TETRAHYDROQUINOLINE
7-NITRO-1,2,3,4-TETRAHYDRO-QUINOLINE HYDROCHLORIDE
7-Nitro-1,2,3,4-Terahydroquinoline
[EINECS(EC#)]

634-828-4
[Molecular Formula]

C9H10N2O2
[MDL Number]

MFCD00496654
[Molecular Weight]

178.19
[MOL File]

30450-62-5.mol
Chemical PropertiesBack Directory
[Melting point ]

61.0 to 65.0 °C
[Boiling point ]

325.2±31.0 °C(Predicted)
[density ]

1.236±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[solubility ]

soluble in Methanol
[form ]

Powder
[pka]

3.44±0.20(Predicted)
[color ]

Red
[CAS DataBase Reference]

30450-62-5(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

T
[Risk Statements ]

25
[Safety Statements ]

45
[RIDADR ]

UN 2811 6.1 / PGIII
[HS Code ]

2933499090
Hazard InformationBack Directory
[Uses]

7-Nitro-1,2,3,4-tetrahydroquinoline is a quinoline compound that can be used as a reagent in chemical reactions or as an intermediate in organic synthesis. It can be used to prepare 7-Aminoquinoline and 7-Nitroquinoline.
[Synthesis]

7-Nitro-1,2,3,4-tetrahydroquinoline is synthesised by the reaction of 1,2,3,4-tetrahydroquinoline and nitric acid in sulphuric acid solution. The specific synthesis steps are as follows:
Concentrated sulfuric acid (30.00 mL) was cooled to -10° C. with an ice/salt bath. To this, 1,2,3,4-tetrahydro-quinoline (10.60 g, 75.60 mmol) and a solution of nitric acid (99.5percent, 4.80 g, 75.60 mmol) in sulfuric acid (15.00 mL) were added simultaneously within 1 hour, so that the temperature of the reaction mixture does not exceed 10° C. The mixture was stirred then for 2.5 hours at -5° C., then poured over ice and treated with sodium carbonate (0.10 kg) until pH 8-9 was reached. The solid was filtered, washing with water, then dissolved in dichloromethane. The organic phase was washed with water, dried over magnesium sulphate and evaporated. 7-Nitro-1,2,3,4-tetrahydro-quinoline was obtained as a viscous brown oil, 13.70 g (85percent), 84percent purity.
7-Nitro-1,2,3,4-tetrahydroquinoline synthesis
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