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4-PIPERAZIN-1-YL-PHENYLAMINE

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4-PIPERAZIN-1-YL-PHENYLAMINE Basic information

Product Name:
4-PIPERAZIN-1-YL-PHENYLAMINE
Synonyms:
  • 4-PIPERAZIN-1-YLANILINE
  • 4-(1-Piperazinyl)aniline, 97%
  • BenzenaMine, 4-(1-piperazinyl)-
  • 4-(4-AMinophenyl)piperazine
  • 1-(4-AMinophenyl)piperazine 97%
  • 1-(4-AMINO-PHENYL)-PIPERAZINE
  • 4-PIPERAZIN-1-YL-PHENYLAMINE
  • 4-PIPERAZINOANILINE
CAS:
67455-41-8
MF:
C10H15N3
MW:
177.25
Product Categories:
  • PIPERIDINE
  • Building Blocks
  • C10
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • pharmacetical
  • Amines
  • Phenyls & Phenyl-Het
  • Phenyls & Phenyl-Het
  • Building Blocks
  • Heterocyclic Building Blocks
  • Piperazines
Mol File:
67455-41-8.mol
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4-PIPERAZIN-1-YL-PHENYLAMINE Chemical Properties

Melting point:
119-123 °C (lit.)
Boiling point:
380.2±27.0 °C(Predicted)
Density 
1.107±0.06 g/cm3(Predicted)
storage temp. 
2-8°C, protect from light
form 
Powder
pka
9.12±0.10(Predicted)
color 
White to purple
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-37/38-41
Safety Statements 
26-39
WGK Germany 
2
HS Code 
2933998090

MSDS

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4-PIPERAZIN-1-YL-PHENYLAMINE Usage And Synthesis

Uses

4-Piperazinoaniline(CAS#67455-41-8)is a important organic intermediate. It can be used in agrochemical, pharmaceutical and dyestuff field.

Synthesis

6269-89-2

67455-41-8

General procedure for the synthesis of 1-(4-aminophenyl)piperazine from 1-(4-nitrophenyl)piperazine: 1-(4-nitrophenyl)piperazine (414 mg, 2 mmol) was dissolved in a mixed solvent of ethanol (15 mL) and tetrahydrofuran (15 mL), and 10% palladium/carbon catalyst (50 mg) was added. The reaction was stirred for 3 h at room temperature under hydrogen atmosphere. The progress of the reaction was monitored by thin layer chromatography (TLC) during the reaction. Upon completion of the reaction, the reaction mixture was filtered through a diatomaceous earth pad to remove the catalyst. The filtrate was concentrated under reduced pressure to afford the target product 1-(4-aminophenyl)piperazine (319 mg, 90.0% yield).

References

[1] Synthetic Communications, 2012, vol. 42, # 2, p. 213 - 222
[2] RSC Advances, 2015, vol. 5, # 113, p. 93433 - 93437
[3] Green Chemistry, 2017, vol. 19, # 14, p. 3400 - 3407
[4] Tetrahedron Letters, 1999, vol. 40, # 31, p. 5655 - 5659
[5] Synthesis and Reactivity in Inorganic, Metal-Organic and Nano-Metal Chemistry, 2011, vol. 41, # 1, p. 114 - 119

4-PIPERAZIN-1-YL-PHENYLAMINESupplier

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