structure of N,N-dimethyl-4-sulfanylbenzamide

N,N-dimethyl-4-sulfanylbenzamide

CAS No.: 62778-80-7
M. Wt: 181.25500
M. Fa: C9H11NOS
InChI Key: -

Names and Identifiers of N,N-dimethyl-4-sulfanylbenzamide

CAS Number

62778-80-7

IUPAC Name

N,N-dimethyl-4-sulfanyl-benzamide

Canonical SMILES

CN(C)C(=O)C1=CC=C(C=C1)S

Physical and chemical properties of N,N-dimethyl-4-sulfanylbenzamide

Exact Mass

181.05600

LogP

1.67710

Molecular Formula

C9H11NOS

Molecular Weight

181.25500

PSA

59.11000

Safety Information of N,N-dimethyl-4-sulfanylbenzamide

Pictograms

Signal Word

Warning

Safety Data Sheet

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

Applications of N,N-dimethyl-4-sulfanylbenzamide

N,N-Dimethyl-4-sulfanylbenzamide has potential applications in various fields:

  • Pharmaceuticals: As a precursor or intermediate in drug synthesis, particularly for compounds targeting microbial infections.
  • Agriculture: Potential use as a pesticide or herbicide due to its biological activity against pests.
  • Chemical Research: Utilized in studies exploring thio compounds and their reactivity.

Interaction Studies of N,N-dimethyl-4-sulfanylbenzamide

Interaction studies have shown that N,N-Dimethyl-4-sulfanylbenzamide can interact with various biological molecules, including:

  • Proteins: Binding studies suggest it may inhibit specific enzymes involved in metabolic pathways.
  • DNA/RNA: Preliminary studies indicate potential intercalation or interaction with nucleic acids, impacting gene expression.

Biological Activity of N,N-dimethyl-4-sulfanylbenzamide

Research indicates that N,N-Dimethyl-4-sulfanylbenzamide may exhibit significant biological activities, including:

  • Antimicrobial Properties: Compounds with sulfanyl groups often show activity against various bacterial strains, potentially due to their ability to disrupt cellular processes.
  • Antioxidant Effects: The presence of sulfur may contribute to antioxidant activity, helping to neutralize free radicals in biological systems.
  • Enzyme Inhibition: This compound may interact with specific enzymes, influencing metabolic pathways.