structure of 1-(2-Methanesulfonyl-6-methoxy-phenyl)-piperazine

1-(2-Methanesulfonyl-6-methoxy-phenyl)-piperazine

CAS No.: 1000018-42-7
M. Wt: 270.348
M. Fa: C12H18N2O3S
InChI Key: IUJWLYYUUWSKMF-UHFFFAOYSA-N

Names and Identifiers of 1000018-42-7

CAS Number

1000018-42-7

MDL Number

MFCD09750908

IUPAC Name

1-(2-methoxy-6-methylsulfonylphenyl)piperazine

InChI

InChI=1S/C12H18N2O3S/c1-17-10-4-3-5-11(18(2,15)16)12(10)14-8-6-13-7-9-14/h3-5,13H,6-9H2,1-2H3

InChIKey

IUJWLYYUUWSKMF-UHFFFAOYSA-N

Canonical SMILES

COC1=C(C(=CC=C1)S(=O)(=O)C)N2CCNCC2

UNSPSC Code

12352100

Physical and chemical properties of 1000018-42-7

Boiling Point

494.5±45.0 °C at 760 mmHg

Density

1.2±0.1 g/cm3

Exact Mass

270.103821

Flash Point

252.9±28.7 °C

H Bond Acceptors

5

H Bond Donors

1

Index of Refraction

1.544

LogP

-0.40

Molecular Formula

C12H18N2O3S

Molecular Weight

270.348

Vapour Pressure

0.0±1.3 mmHg at 25°C

Safety Information of 1000018-42-7

Pictograms

Signal Word

 Warning

Safety Data Sheet
Supports customized editing of SDS information and downloading in PDF documents.

Applications of 1000018-42-7

1-(2-Methanesulfonyl-6-methoxy-phenyl)-piperazine has several applications:

  • Pharmaceutical Development: It serves as a precursor in synthesizing various pharmaceuticals, particularly those targeting neurological disorders due to its psychoactive potential.
  • Material Science: The compound is used in developing new materials with specific chemical properties.
  • Biological Research: It is employed in studying protein interactions and enzyme functions within biological systems.

Interaction Studies of 1000018-42-7

Interaction studies involving 1-(2-Methanesulfonyl-6-methoxy-phenyl)-piperazine focus on its binding affinity to various biological targets. These studies help elucidate the compound's mechanism of action and potential therapeutic uses. For instance, investigations into its inhibitory effects on certain enzymes could reveal pathways for drug development aimed at treating conditions like depression or anxiety.

Biological Activity of 1000018-42-7

1-(2-Methanesulfonyl-6-methoxy-phenyl)-piperazine exhibits various biological activities, primarily due to its interaction with biological targets such as enzymes and receptors. The presence of the sulfonyl group enhances its potential to inhibit specific enzymes, which may lead to therapeutic effects. Research indicates that piperazine derivatives often possess psychoactive properties, making them candidates for further studies in pharmacology.