structure of 2-(2-Chlorophenyl)-2-(Pyrrolidin-1-Yl)Acetamide

2-(2-Chlorophenyl)-2-(Pyrrolidin-1-Yl)Acetamide

CAS No.: 1000340-02-2
M. Wt: 238.71
M. Fa: C12H15ClN2O
InChI Key: IBDCMDIMPLMCLX-UHFFFAOYSA-N

Names and Identifiers of 1000340-02-2

CAS Number

1000340-02-2

MDL Number

MFCD09910404

IUPAC Name

2-(2-chlorophenyl)-2-pyrrolidin-1-ylacetamide

InChI

InChI=1S/C12H15ClN2O/c13-10-6-2-1-5-9(10)11(12(14)16)15-7-3-4-8-15/h1-2,5-6,11H,3-4,7-8H2,(H2,14,16)

InChIKey

IBDCMDIMPLMCLX-UHFFFAOYSA-N

Canonical SMILES

NC(=O)C(C1=CC=CC=C1Cl)N1CCCC1

UNSPSC Code

12352100

Physical and chemical properties of 1000340-02-2

Molecular Formula

C12H15ClN2O

Molecular Weight

238.71

Safety Information of 1000340-02-2

Pictograms

Signal Word

 Warning

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

Applications of 1000340-02-2

The potential applications of 2-(2-Chlorophenyl)-2-(pyrrolidin-1-YL)acetamide include:

  • Pharmaceutical Development: Due to its biological activity, it may serve as a lead compound in the development of new medications targeting neurological disorders.
  • Research Tool: It can be used in laboratory settings to study ion channel modulation and neurotransmitter dynamics.

Interaction Studies of 1000340-02-2

Interaction studies involving 2-(2-Chlorophenyl)-2-(pyrrolidin-1-YL)acetamide focus on its effects on various receptors and enzymes:

  • Enzyme Inhibition: The compound has been evaluated for its inhibitory effects on monoamine oxidases (MAO-A and MAO-B), which are important in neurotransmitter metabolism .
  • Receptor Binding Affinity: Studies have assessed its binding affinity to various neurotransmitter receptors, indicating potential therapeutic targets.

Biological Activity of 1000340-02-2

Research indicates that 2-(2-Chlorophenyl)-2-(pyrrolidin-1-YL)acetamide exhibits significant biological activity, particularly in modulating neurotransmitter systems. It has been studied for its potential as:

  • Anticonvulsant Agent: The compound has shown promise in preclinical studies for its anticonvulsant properties, suggesting it may be effective in treating epilepsy or seizure disorders .
  • Modulator of Ion Channels: Some studies have indicated that compounds with similar structures can act as modulators of potassium channels, which are crucial for neuronal excitability .