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Details

Stereochemistry ACHIRAL
Molecular Formula C10H14N2
Molecular Weight 162.2316
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-PHENYLPIPERAZINE

SMILES

C1CN(CCN1)C2=CC=CC=C2

InChI

InChIKey=YZTJYBJCZXZGCT-UHFFFAOYSA-N
InChI=1S/C10H14N2/c1-2-4-10(5-3-1)12-8-6-11-7-9-12/h1-5,11H,6-9H2

HIDE SMILES / InChI

Molecular Formula C10H14N2
Molecular Weight 162.2316
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Specific labelling of serotonin 5-HT(1B) receptors in rat frontal cortex with the novel, phenylpiperazine derivative, [3H]GR125,743. A pharmacological characterization.
2002 Apr
New pyrimido[5,4-b]indoles as ligands for alpha(1)-adrenoceptor subtypes.
2003 Jul 3
Rhodium-catalyzed anti-Markovnikov hydroamination of vinylarenes.
2003 May 14
Synthesis of totarol amino alcohol derivatives and their antiplasmodial activity and cytotoxicity.
2003 Oct 1
Synthesis and serotonergic activity of variously substituted (3-amido)phenylpiperazine derivatives and benzothiophene-4-piperazine derivatives: novel antagonists for the vascular 5-HT1B receptor.
2004 Apr
Dopamine D4 ligands and models of receptor activation: 2-(4-pyridin-2-ylpiperazin-1-ylmethyl)-1H-benzimidazole and related heteroarylmethylarylpiperazines exhibit a substituent effect responsible for additional efficacy tuning.
2004 Apr 22
Synthesis and radioiodination of selective ligands for the dopamine D3 receptor subtype.
2004 Aug 2
Synthesis of novel N-alkyl carbamates of a-substituted amides of g-hydroxybutyric acid as potential acetylcholinesterase inhibitors.
2004 Dec
1- and 2-substituted naphthalenes: a new class of potential hypotensive agents.
2004 Jun 7
Use of physicochemical calculation of pKa and CLogP to predict phospholipidosis-inducing potential: a case study with structurally related piperazines.
2004 Mar
Discovery of a potent and selective alpha v beta 3 integrin antagonist with strong inhibitory activity against neointima formation in rat balloon injury model.
2004 May 17
Prediction of genotoxicity of chemical compounds by statistical learning methods.
2005 Jun
Oxidative transformation of fluoroquinolone antibacterial agents and structurally related amines by manganese oxide.
2005 Jun 15
Synthesis and biological evaluation of new thiazolyl/benzothiazolyl-amides, derivatives of 4-phenyl-piperazine.
2005 Nov-Dec
Complete assignments of 1H and 13C NMR data for ten phenylpiperazine derivatives.
2005 Oct
Hepatic metabolism of two alpha-1A-adrenergic receptor antagonists, phthalimide-phenylpiperazine analogs (RWJ-69205 and RWJ-69471), in the rat, dog and human.
2006 Oct-Dec
Adsorption and oxidation of fluoroquinolone antibacterial agents and structurally related amines with goethite.
2007 Jan
FT-IR and NMR investigation of 1-phenylpiperazine: a combined experimental and theoretical study.
2007 Jul
Identification of metabolites produced from N-phenylpiperazine by Mycobacterium spp.
2007 Mar
Determination of lipophilicity of alpha-(4-phenylpiperazine) derivatives of N-benzylamides using chromatographic and computational methods.
2008 Apr
FT-IR spectroscopic investigation of some Hofmann type complexes: M(1-phenylpiperazine)2Ni(CN)4 (M=Ni, Co, Cd, Pd or Mn).
2008 Jul
Serotonergic neurotransmission mediates hypothermia induced by the N-phenylpiperazine antipsychotic prototypes LASSBio-579 and LASSBio-581.
2008 Mar
Acaricidal properties of piperazine and its derivatives against house-dust and stored-food mites.
2009 Jun
Evaluation of D2 and D3 dopamine receptor selective compounds on L-dopa-dependent abnormal involuntary movements in rats.
2009 May-Jun
Application of a library of artificial receptors formed by the self-organization of N-lipidated peptides immobilized on cellulose in studying the effects of the incorporation of a fluorine atom.
2009 May-Jun
Animal violence demystified.
2010
Oxidation of fluoroquinolone antibiotics and structurally related amines by chlorine dioxide: Reaction kinetics, product and pathway evaluation.
2010 Dec
Design of new dopamine D2 receptor ligands: biosynthesis and pharmacological evaluation of the hydroxylated metabolite of LASSBio-581.
2010 May 1
Analysis of phenylpiperazine-like stimulants in human hair as trimethylsilyl derivatives by gas chromatography-mass spectrometry.
2010 Oct 1
Search for influence of spatial properties on affinity at α1-adrenoceptor subtypes for phenylpiperazine derivatives of phenytoin.
2010 Oct 15
Novel tricyclic pyrazole BRAF inhibitors with imidazole or furan central scaffolds.
2010 Sep 15
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:23:35 GMT 2025
Edited
by admin
on Mon Mar 31 19:23:35 GMT 2025
Record UNII
J9225CBI7D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1-PHENYLPIPERAZINE
Systematic Name English
N-PHENYLDIETHYLENEDIAMINE
Preferred Name English
PHENYLPIPERAZINE, 1-
Systematic Name English
LEVODROPROPIZINE IMPURITY B [EP IMPURITY]
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID8057855
Created by admin on Mon Mar 31 19:23:35 GMT 2025 , Edited by admin on Mon Mar 31 19:23:35 GMT 2025
PRIMARY
MESH
C031503
Created by admin on Mon Mar 31 19:23:35 GMT 2025 , Edited by admin on Mon Mar 31 19:23:35 GMT 2025
PRIMARY
PUBCHEM
7096
Created by admin on Mon Mar 31 19:23:35 GMT 2025 , Edited by admin on Mon Mar 31 19:23:35 GMT 2025
PRIMARY
WIKIPEDIA
Phenylpiperazine
Created by admin on Mon Mar 31 19:23:35 GMT 2025 , Edited by admin on Mon Mar 31 19:23:35 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-165-6
Created by admin on Mon Mar 31 19:23:35 GMT 2025 , Edited by admin on Mon Mar 31 19:23:35 GMT 2025
PRIMARY
FDA UNII
J9225CBI7D
Created by admin on Mon Mar 31 19:23:35 GMT 2025 , Edited by admin on Mon Mar 31 19:23:35 GMT 2025
PRIMARY
CAS
92-54-6
Created by admin on Mon Mar 31 19:23:35 GMT 2025 , Edited by admin on Mon Mar 31 19:23:35 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP