structure of 5-amino-1-(4-methylphenyl)-1H-pyrazole-4-carboxamide

5-amino-1-(4-methylphenyl)-1H-pyrazole-4-carboxamide

CAS No.: 100061-56-1
M. Wt: 216.23900
M. Fa: C11H12N4O
InChI Key: MXBYCCRXPQPHBP-UHFFFAOYSA-N

Names and Identifiers of 100061-56-1

CAS Number

100061-56-1

IUPAC Name

5-amino-1-(4-methylphenyl)pyrazole-4-carboxamide

InChI

InChI=1S/C11H12N4O/c1-7-2-4-8(5-3-7)15-10(12)9(6-14-15)11(13)16/h2-6H,12H2,1H3,(H2,13,16)

InChIKey

MXBYCCRXPQPHBP-UHFFFAOYSA-N

Canonical SMILES

CC1=CC=C(C=C1)N2C(=C(C=N2)C(=O)N)N

Physical and chemical properties of 100061-56-1

Exact Mass

216.10100

LogP

2.32720

Molecular Formula

C11H12N4O

Molecular Weight

216.23900

PSA

87.92000

Safety Information of 100061-56-1

Pictograms

Signal Word

Warning

Safety Data Sheet

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

Applications of 100061-56-1

5-amino-1-(4-methylphenyl)-1H-pyrazole-4-carboxamide has several applications in various fields:

  • Pharmaceutical Development: Due to its biological activity, it is being explored for potential use as an anticancer or anti-inflammatory agent.
  • Chemical Research: It serves as a reference standard in laboratories for research involving pyrazole derivatives.
  • Agricultural Chemistry: There is potential for its use in developing agrochemicals due to its antimicrobial properties.

Interaction Studies of 100061-56-1

Studies on the interactions of 5-amino-1-(4-methylphenyl)-1H-pyrazole-4-carboxamide with biological targets are crucial for understanding its mechanism of action. These studies typically involve:

  • Binding Affinity Assessments: Evaluating how well the compound binds to specific enzymes or receptors related to its proposed therapeutic effects.
  • Cell Line Studies: Testing its efficacy against various cancer cell lines to determine cytotoxic effects and potential pathways involved.

Such studies are essential for elucidating its pharmacodynamics and pharmacokinetics.

Biological Activity of 100061-56-1

Research indicates that 5-amino-1-(4-methylphenyl)-1H-pyrazole-4-carboxamide exhibits various biological activities, primarily due to its structural characteristics. It has shown potential in:

  • Antitumor Activity: Some studies suggest that this compound may inhibit the growth of certain cancer cell lines, making it a candidate for further investigation in oncology.
  • Anti-inflammatory Effects: The compound may possess anti-inflammatory properties, which could be beneficial in treating conditions associated with inflammation.
  • Antimicrobial Properties: Preliminary studies have indicated potential antimicrobial activity against various pathogens.

These biological activities highlight its potential as a lead compound in drug discovery.

Retrosynthesis analysis of 100061-56-1

  • Route#1

    Cas:103646-82-8
    Cas:100061-56-1