Basic information Safety Supplier Related

2-(4-METHYLPIPERAZINO)BENZALDEHYDE

Basic information Safety Supplier Related

2-(4-METHYLPIPERAZINO)BENZALDEHYDE Basic information

Product Name:
2-(4-METHYLPIPERAZINO)BENZALDEHYDE
Synonyms:
  • BUTTPARK 33\06-51
  • 2-(4-METHYLPIPERAZIN-1-YL)BENZALDEHYDE
  • 2-(4-METHYLPIPERAZINO)BENZALDEHYDE
  • 2-(4-Methylpiperazino)benzadehyde
  • 2-(4-methyl-1-piperazin-4-iumyl)benzaldehyde
  • Benzaldehyde, 2-(4-methyl-1-piperazinyl)-
  • 2-(4-Methyl-1-piperazinyl)benzaldehyde
CAS:
85803-62-9
MF:
C12H16N2O
MW:
204.27
Product Categories:
  • Amino Acid Derivatives
Mol File:
85803-62-9.mol
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2-(4-METHYLPIPERAZINO)BENZALDEHYDE Chemical Properties

Melting point:
44 °C
Boiling point:
110
Density 
1.107±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
7.69±0.42(Predicted)
Appearance
Colorless to light yellow Liquid
CAS DataBase Reference
85803-62-9(CAS DataBase Reference)
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Safety Information

Hazard Codes 
C,Xi
Risk Statements 
36/37/38-36
Safety Statements 
26-36/37/39
Hazard Note 
Corrosive
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2-(4-METHYLPIPERAZINO)BENZALDEHYDE Usage And Synthesis

Synthesis

109-01-3

446-52-6

85803-62-9

General procedure: 2-fluorobenzaldehyde (20.0 mL, 189.9 mmol), 1-methylpiperazine (33.0 mL, 297.7 mmol) and potassium carbonate (40.0 g, 289.4 mmol) were dissolved in water (200 mL) and heated to reflux. After the reaction was completed, it was cooled to room temperature and the reaction mixture was extracted with ethyl acetate (2 x 150 mL). The organic phases were combined, washed with brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to afford the target product 2-(4-methylpiperazine)benzaldehyde (PP57, 38.6 g, 100%) as an orange oil. Its NMR hydrogen spectrum (CDCl3) data were as follows: δ 10.10 (s, 1H), 7.77 (dd, J = 7.9, 1.7 Hz, 1H), 7.51-7.48 (m, 1H), 7.10-7.06 (m, 2H), 3.11 (t, J = 4.6 Hz, 4H), 2.63 (br s, 4H), 2.36 (s, 3H) .

References

[1] Patent: WO2006/48727, 2006, A1. Location in patent: Page/Page column 83
[2] Patent: US2003/87914, 2003, A1
[3] Russian Chemical Bulletin, 2004, vol. 53, # 6, p. 1240 - 1247
[4] Chemical Communications, 2017, vol. 53, # 75, p. 10448 - 10451
[5] Synthesis, 1987, # 7, p. 641 - 645

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