Basic information Safety Supplier Related

1-(2-Chlorophenyl)piperazine hydrochloride

Basic information Safety Supplier Related

1-(2-Chlorophenyl)piperazine hydrochloride Basic information

Product Name:
1-(2-Chlorophenyl)piperazine hydrochloride
Synonyms:
  • TIMTEC-BB SBB003263
  • LABOTEST-BB LT00159499
  • LABOTEST-BB LT00454957
  • 1-(O-CHLOROPHENYL)PIPERAZINE HYDROCHLORIDE
  • N-(2-CHLOROPHENYL)PIPERAZINE MONOHYDROCHLORIDE
  • 1-(2-CHLOROPHENYL)PIPERAZINE HYDROCHLORIDE
  • 1-(2-CHLOROPHENYL)PIPERAZINE MONOHYDROCHLORIDE
  • 1-(2-chlorophenyl)piperazinium chloride
CAS:
41202-32-8
MF:
C10H14Cl2N2
MW:
233.14
EINECS:
255-262-0
Product Categories:
  • Piperidines, Piperidones, Piperazines
  • PiperazineDerivative
  • Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Piperazines
  • PiperazinesHeterocyclic Building Blocks
Mol File:
41202-32-8.mol
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1-(2-Chlorophenyl)piperazine hydrochloride Chemical Properties

Melting point:
160-163 °C (dec.)(lit.)
storage temp. 
Store at room temperature
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Solid
color 
White
Sensitive 
Hygroscopic
BRN 
5652889
CAS DataBase Reference
41202-32-8(CAS DataBase Reference)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
WGK Germany 
3

MSDS

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1-(2-Chlorophenyl)piperazine hydrochloride Usage And Synthesis

Uses

1-(2-Chlorophenyl)piperazine Hydrochloride is a reactant used in the preparation of piperazinyl, phenylpiperidinyl, tetrahydropyridinyl, and tetrahydropyridoindolylbutylbenzindoles with 5-hydroxytryptamine receptor antagonist activity.

Synthesis

1104513-49-6

41202-32-8

To a stirred solution of tert-butyl 4-(2-chlorophenyl)piperazine-1-carboxylate (250 mg, 0.844 mmol) in 1,4-dioxane (2 mL) was added slowly and dropwise a 1,4-dioxane solution (0.9 mL, 3.60 mmol) in 4 N HCl at 0 °C. The reaction mixture was gradually warmed to room temperature and stirred continuously for 4 h (complete consumption of feedstock was confirmed by TLC monitoring). Upon completion of the reaction, the volatile solvent was removed under reduced pressure to give the crude product. The crude product was washed with ether (2 x 20 mL) and dried under high vacuum to yield 1-(2-chlorophenyl)piperazine hydrochloride (165 mg, 84% yield) as a white solid.

References

[1] Patent: WO2018/125961, 2018, A1. Location in patent: Page/Page column 45; 46

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