Basic information Safety Supplier Related

2-PIPERAZIN-1-YL-BENZALDEHYDE

Basic information Safety Supplier Related

2-PIPERAZIN-1-YL-BENZALDEHYDE Basic information

Product Name:
2-PIPERAZIN-1-YL-BENZALDEHYDE
Synonyms:
  • 2-PIPERAZIN-1-YL-BENZALDEHYDE
  • Benzaldehyde, 2-(1-piperazinyl)- (9CI)
  • 1-(2-Formylphenyl)piperazine
  • 2-(1-piperazinyl)benzaldehyde
  • Benzaldehyde, 2-(1-piperazinyl)-
CAS:
736991-52-9
MF:
C11H14N2O
MW:
190.24
Product Categories:
  • PIPERIDINE
  • API intermediates
Mol File:
736991-52-9.mol
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2-PIPERAZIN-1-YL-BENZALDEHYDE Chemical Properties

Boiling point:
355.0±27.0 °C(Predicted)
Density 
1.123±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
8.86±0.10(Predicted)
CAS DataBase Reference
736991-52-9(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
Hazard Note 
Irritant
HS Code 
2933599590
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2-PIPERAZIN-1-YL-BENZALDEHYDE Usage And Synthesis

Synthesis

110-85-0

446-52-6

736991-52-9

General procedure for the synthesis of 2-piperazine-1-benzaldehyde from piperazine and 2-fluorobenzaldehyde: 2-fluorobenzaldehyde (1.0 g, 8.1 mmol) was dissolved in N,N-dimethylformamide (15 ml) in a 50 ml round bottom flask. Piperazine (836 mg, 9.7 mmol) and potassium carbonate (1.68 g, 12.2 mmol) were then added and the reaction was carried out at 130 °C for 6 hours. After completion of the reaction, it was cooled to room temperature, the reaction mixture was diluted with water and extracted with ethyl acetate. The organic phases were combined and dried over anhydrous sodium sulfate. Purification was carried out by silica gel column chromatography (petroleum ether: ethyl acetate = 5:1; dichloromethane: methanol = 10:1), and the target compound 2-piperazine-1-benzaldehyde (760 mg, 49.4% yield) was obtained after concentration.

References

[1] Patent: CN105777632, 2016, A. Location in patent: Paragraph 0481; 0482; 0483

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