structure of N-(4-fluorophenyl)-3-hydroxybenzamide

N-(4-fluorophenyl)-3-hydroxybenzamide

CAS No.: 97480-96-1
M. Wt: 231.22
M. Fa: C13H10FNO2
InChI Key: HNEJDARAUWWGIN-UHFFFAOYSA-N

Names and Identifiers of N-(4-fluorophenyl)-3-hydroxybenzamide

CAS Number

97480-96-1

MDL Number

MFCD11131047

IUPAC Name

N-(4-fluorophenyl)-3-hydroxybenzamide

InChI

InChI=1S/C13H10FNO2/c14-10-4-6-11(7-5-10)15-13(17)9-2-1-3-12(16)8-9/h1-8,16H,(H,15,17)

InChIKey

HNEJDARAUWWGIN-UHFFFAOYSA-N

Canonical SMILES

C1=CC(=CC(=C1)O)C(=O)NC2=CC=C(C=C2)F

UNSPSC Code

12352100

Physical and chemical properties of N-(4-fluorophenyl)-3-hydroxybenzamide

Acidity coefficient

9.20±0.10(Predicted)

Boiling Point

313.8±27.0 °C at 760 mmHg

Density

1.352±0.06 g/cm3(Predicted)

H Bond Acceptors

2

H Bond Donors

2

LogP

2.90426723633333

Molecular Formula

C13H10FNO2

Molecular Weight

231.22

Safety Information of N-(4-fluorophenyl)-3-hydroxybenzamide

Pictograms

Signal Word

 Warning

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

Applications of N-(4-fluorophenyl)-3-hydroxybenzamide

N-(4-fluorophenyl)-3-hydroxybenzamide has several potential applications:

  • Pharmaceutical Development: Its structural characteristics make it a candidate for drug development, particularly in targeting bacterial and viral infections.
  • Research Tool: It can serve as a model compound in studies related to enzyme inhibition and drug-receptor interactions.
  • Material Science: The unique properties of this compound may allow for applications in creating advanced materials or coatings.

Interaction Studies of N-(4-fluorophenyl)-3-hydroxybenzamide

Studies investigating the interactions of N-(4-fluorophenyl)-3-hydroxybenzamide with biological targets have highlighted its potential efficacy:

  • Molecular Docking Studies: These studies suggest favorable binding interactions with specific protein targets, indicating its potential as a lead compound for drug design.
  • Binding Affinity Assessments: Quantitative evaluations reveal promising binding affinities, which are critical for assessing its viability as a therapeutic agent.

Biological Activity of N-(4-fluorophenyl)-3-hydroxybenzamide

The biological activity of N-(4-fluorophenyl)-3-hydroxybenzamide has been explored in various studies, indicating potential therapeutic properties:

  • Antimicrobial Activity: Research has shown that similar compounds exhibit antibacterial and antiviral properties, suggesting that N-(4-fluorophenyl)-3-hydroxybenzamide may also possess such activities.
  • Enzyme Inhibition: The compound may act as an inhibitor for certain enzymes involved in disease processes, making it a candidate for further pharmacological studies.
  • Toxicity Profiles: Preliminary toxicity assessments indicate that derivatives of this compound may have favorable safety profiles, making them suitable for further development as pharmaceuticals.