structure of N-(3-cyanophenyl)furan-2-carboxamide

N-(3-cyanophenyl)furan-2-carboxamide

CAS No.: 349644-67-3
M. Wt: 212.204
M. Fa: C12H8N2O2
InChI Key: -

Names and Identifiers of N-(3-cyanophenyl)furan-2-carboxamide

CAS Number

349644-67-3

IUPAC Name

N-(3-cyanophenyl)furan-2-carboxamide

Canonical SMILES

C1=CC(=CC(=C1)NC(=O)C2=CC=CO2)C#N

Physical and chemical properties of N-(3-cyanophenyl)furan-2-carboxamide

Boiling Point

272.4±20.0 °C at 760 mmHg

Density

1.3±0.1 g/cm3

Exact Mass

212.058578

Flash Point

118.5±21.8 °C

Index of Refraction

1.612

LogP

2.48

Molecular Formula

C12H8N2O2

Molecular Weight

212.204

Vapour Pressure

0.0±0.6 mmHg at 25°C

Safety Information of N-(3-cyanophenyl)furan-2-carboxamide

Pictograms

Signal Word

 Warning

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

Applications of N-(3-cyanophenyl)furan-2-carboxamide

N-(3-cyanophenyl)furan-2-carboxamide has several applications:

  • Chemistry: It serves as a building block in the synthesis of more complex organic molecules.
  • Biology: Its potential biological activities make it a candidate for drug development, particularly in targeting microbial infections and cancer cells.
  • Industry: The compound may be utilized in developing new materials or specialty chemicals due to its unique structural features.

Interaction Studies of N-(3-cyanophenyl)furan-2-carboxamide

Interaction studies are essential for understanding how N-(3-cyanophenyl)furan-2-carboxamide interacts with biological systems. These studies often involve molecular docking simulations to evaluate binding affinities with specific targets, such as enzymes or receptors involved in disease pathways. Investigating these interactions helps elucidate its mechanism of action and potential therapeutic applications.

Biological Activity of N-(3-cyanophenyl)furan-2-carboxamide

Research indicates that N-(3-cyanophenyl)furan-2-carboxamide possesses potential biological activities, particularly in the realms of antimicrobial and anticancer properties. Compounds containing furan rings have been noted for their significant biological activities, and N-(3-cyanophenyl)furan-2-carboxamide is being investigated for its efficacy against various pathogens and cancer cell lines. Its structural features may contribute to its ability to interact with biological targets effectively.