structure of 2-(4-Ethoxyanilino)acetohydrazide

2-(4-Ethoxyanilino)acetohydrazide

CAS No.: 100133-39-9
M. Wt: 209.24500
M. Fa: C10H15N3O2
InChI Key: SBGTZGYSJPRABB-UHFFFAOYSA-N

Names and Identifiers of 2-(4-Ethoxyanilino)acetohydrazide

CAS Number

100133-39-9

MDL Number

MFCD02255627

IUPAC Name

2-(4-ethoxyanilino)acetohydrazide

InChI

InChI=1S/C10H15N3O2/c1-2-15-9-5-3-8(4-6-9)12-7-10(14)13-11/h3-6,12H,2,7,11H2,1H3,(H,13,14)

InChIKey

SBGTZGYSJPRABB-UHFFFAOYSA-N

Canonical SMILES

CCOC1=CC=C(C=C1)NCC(=O)NN

UNSPSC Code

12352100

Physical and chemical properties of 2-(4-Ethoxyanilino)acetohydrazide

Exact Mass

209.11600

LogP

1.65130

Molecular Formula

C10H15N3O2

Molecular Weight

209.24500

PSA

76.38000

Safety Information of 2-(4-Ethoxyanilino)acetohydrazide

Pictograms

Signal Word

 Warning

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

Applications of 2-(4-Ethoxyanilino)acetohydrazide

2-(4-Ethoxyanilino)acetohydrazide finds applications in several fields:

  • Organic Synthesis: It serves as a building block for synthesizing more complex organic molecules.
  • Pharmaceutical Research: Due to its biological activity, it is investigated for potential pharmaceutical applications, particularly as an antimicrobial or antioxidant agent.
  • Analytical Chemistry: The compound can be used as a reagent in qualitative analysis for detecting carbonyl compounds through hydrazone formation.

Interaction Studies of 2-(4-Ethoxyanilino)acetohydrazide

Studies on the interactions of 2-(4-Ethoxyanilino)acetohydrazide with various biological molecules have shown:

  • Enzyme Inhibition: Preliminary data suggest that it may inhibit certain enzymes involved in metabolic pathways, which could contribute to its observed biological effects.
  • Binding Affinity: The compound's ability to form hydrogen bonds and engage in π-π stacking interactions may enhance its binding affinity to target proteins.

These interactions are crucial for understanding its mechanism of action and potential therapeutic uses.

Biological Activity of 2-(4-Ethoxyanilino)acetohydrazide

Research indicates that 2-(4-Ethoxyanilino)acetohydrazide exhibits notable biological activities, including:

  • Antimicrobial Properties: Studies suggest that this compound possesses antimicrobial effects against various bacterial strains.
  • Antioxidant Activity: It has been observed to scavenge free radicals, indicating potential applications in preventing oxidative stress-related damage.
  • Pharmacological Potential: The compound's structure suggests it may interact with biological targets, potentially leading to therapeutic effects in conditions like inflammation or cancer.