structure of 1-[(2-Fluoro-4-phenylsulfonyl)phenyl]piperazine

1-[(2-Fluoro-4-phenylsulfonyl)phenyl]piperazine

CAS No.: 1000339-97-8
M. Wt: 320.382
M. Fa: C16H17FN2O2S
InChI Key: QDJNVLAMKGYDKO-UHFFFAOYSA-N

Names and Identifiers of 1000339-97-8

CAS Number

1000339-97-8

IUPAC Name

1-[4-(benzenesulfonyl)-2-fluorophenyl]piperazine

InChI

InChI=1S/C16H17FN2O2S/c17-15-12-14(22(20,21)13-4-2-1-3-5-13)6-7-16(15)19-10-8-18-9-11-19/h1-7,12,18H,8-11H2

InChIKey

QDJNVLAMKGYDKO-UHFFFAOYSA-N

Canonical SMILES

C1CN(CCN1)C2=C(C=C(C=C2)S(=O)(=O)C3=CC=CC=C3)F

Physical and chemical properties of 1000339-97-8

Boiling Point

518.3±50.0 °C at 760 mmHg

Density

1.3±0.1 g/cm3

Exact Mass

320.099487

Flash Point

267.2±30.1 °C

Index of Refraction

1.589

LogP

2.23

Molecular Formula

C16H17FN2O2S

Molecular Weight

320.382

Vapour Pressure

0.0±1.4 mmHg at 25°C

Applications of 1000339-97-8

1-[(2-Fluoro-4-phenylsulfonyl)phenyl]piperazine has potential applications in various fields:

  • Pharmaceuticals: As a candidate for antidepressant or anxiolytic medications due to its serotonin reuptake inhibition.
  • Agriculture: As an acaricide or pesticide due to its demonstrated biological activity against pests.
  • Chemical Research: As a building block for synthesizing other biologically active compounds.

Interaction Studies of 1000339-97-8

Interaction studies involving 1-[(2-Fluoro-4-phenylsulfonyl)phenyl]piperazine have focused on its binding affinity to serotonin receptors and other neurotransmitter systems. These studies aim to elucidate the mechanism of action and potential side effects associated with its use as a therapeutic agent. The compound's interactions with various biological targets are critical for understanding its pharmacological profile and therapeutic potential.

Biological Activity of 1000339-97-8

Research has indicated that 1-[(2-Fluoro-4-phenylsulfonyl)phenyl]piperazine exhibits significant biological activity. It has been explored for its potential as a serotonin reuptake inhibitor, which may make it useful in treating conditions such as depression and anxiety disorders. Furthermore, studies have shown that derivatives of phenylpiperazines possess acaricidal properties, suggesting that this compound could also have applications in pest control.