1-(2-Methoxyphenyl)piperazine

1-(2-Methoxyphenyl)piperazine
  • CAS No.:35386-24-4
Other grades of this product :
1-(2-Methoxyphenyl)piperazine Basic information
Product Name:1-(2-Methoxyphenyl)piperazine
Synonyms:RARECHEM AH CK 0126;TIMTEC-BB SBB003620;Urapidil Impurity 6;LABOTEST-BB LT00233095;AKOS BBS-00003584;1-(2-METHOXYLPHENYL)-PIPERAZINE;2-(PIPERAZIN-1-YL)METHOXYBENZENE;2-(1-PIPERAZINYL)ANISOLE
CAS:35386-24-4
MF:C11H16N2O
MW:192.26
EINECS:252-537-7
Product Categories:Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Bioactive Small Molecules;C11;Piperidines, Piperidones, Piperazines;API intermediates;(intermediate of urapidil);Building Blocks;Heterocyclic Building Blocks;Piperazines;Cell Biology;Chemical Synthesis;BUILDING BLOCKS;Piperaizine;Heterocyclic Building Blocks;M
Mol File:35386-24-4.mol
1-(2-Methoxyphenyl)piperazine Chemical Properties
Melting point 35-40 °C (lit.)
Boiling point 130-133 °C/0.1 mmHg (lit.)
density 1.095 g/mL at 25 °C (lit.)
refractive index n20/D 1.575(lit.)
Fp >230 °F
storage temp. Keep in dark place,Inert atmosphere,Room temperature
form Liquid After Melting
pka8.98±0.10(Predicted)
color Clear colorless to yellow
Water Solubility Soluble in chloroform, ethyl acetate, and methanol. Insoluble in water
Sensitive Air Sensitive
BRN 167888
LogP1.67
CAS DataBase Reference35386-24-4(CAS DataBase Reference)
Safety Information
Hazard Codes C,Xi
Risk Statements 34-36/37/38
Safety Statements 26-36/37/39-45-28A-36
RIDADR UN 3263 8/PG 3
WGK Germany 3
3-10
Hazard Note Irritant
HazardClass 8
PackingGroup 
HS Code 29349990
MSDS Information
ProviderLanguage
1-(2-Methoxyphenyl)piperazine English
SigmaAldrich English
ACROS English
ALFA English
1-(2-Methoxyphenyl)piperazine Usage And Synthesis
Chemical Propertiesclear colorless to yellow liquid after melting
UsesA piperazine derivative and a selective antagonist at D3 receptors that influences the expression of cocaine-induced conditioned place preference (CPP).
UsesIt is used as pharmaceutical intermediate. N-alkylated 1-(2-methyoxyphenyl)piperazines markedly improved affinity and selectivity of the dopamine D3 receptor which is recognized as a potential therapeutic target for the treatment of various neurological and psychiatric disorders.
Uses1-(2-Methoxyphenyl)piperazine can be used:
  • To functionalize pyrazolylvinyl ketones via Aza-Michael addition reaction.
  • To prepare cyclic amine substituted Tr?ger′s base derivatives.
  • To prepare functionalized bis(mercaptoimidazolyl)borates by reacting with the activated ester, [(1-methyl-2-mercaptoimidazol-5-yl)carbonyl]succinimide.

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