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7-Nitro-1,2,3,4-tetrahydroquinoline

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7-Nitro-1,2,3,4-tetrahydroquinoline Basic information

Product Name:
7-Nitro-1,2,3,4-tetrahydroquinoline
Synonyms:
  • 7-Nitro-1,2,3,4-Terahydroquinoline
  • 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-tetrahydroquinoline 1,2,3,4-Tetrahydro-7-nitroquinoline
  • Quinoline, 1,2,3,4-tetrahydro-7-nitro-
  • 7-Nitro-1,2,3,4-tetrahydroquinoline>
  • 7-Nitro-1,2,3,4-tetrahydroquinoline,95%
CAS:
30450-62-5
MF:
C9H10N2O2
MW:
178.19
EINECS:
634-828-4
Product Categories:
  • Quinoline&Isoquinoline
Mol File:
30450-62-5.mol
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7-Nitro-1,2,3,4-tetrahydroquinoline Chemical Properties

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
pka
3.44±0.20(Predicted)
form 
Powder
color 
Red
CAS DataBase Reference
30450-62-5(CAS DataBase Reference)
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Safety Information

Hazard Codes 
T
Risk Statements 
25
Safety Statements 
45
RIDADR 
UN 2811 6.1 / PGIII
HS Code 
2933499090
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7-Nitro-1,2,3,4-tetrahydroquinoline Usage And Synthesis

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.

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