structure of 5-aminothiadiazole-4-carbothioamide

5-aminothiadiazole-4-carbothioamide

CAS No.: 100097-66-3
M. Wt: 160.22100
M. Fa: C3H4N4S2
InChI Key: -

Names and Identifiers of 5-aminothiadiazole-4-carbothioamide

CAS Number

100097-66-3

IUPAC Name

5-azanyl-1,2,3-thiadiazole-4-carbothioamide

Canonical SMILES

C1(=C(SN=N1)N)C(=S)N

Physical and chemical properties of 5-aminothiadiazole-4-carbothioamide

Exact Mass

159.98800

LogP

1.03600

Molecular Formula

C3H4N4S2

Molecular Weight

160.22100

PSA

138.15000

Safety Information of 5-aminothiadiazole-4-carbothioamide

Pictograms

Signal Word

Warning

Safety Data Sheet

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

Applications of 5-aminothiadiazole-4-carbothioamide

1,2,3-Thiadiazole-4-carbothioamide, 5-amino- has potential applications across various fields:

  • Pharmaceutical Development: Due to its biological activity, it may serve as a lead compound in drug discovery for antimicrobial or anticancer agents.
  • Agricultural Chemicals: Its properties could be explored for developing new pesticides or fungicides.
  • Material Science: The unique structure may lend itself to applications in creating novel materials with specific electronic or optical properties.

Interaction Studies of 5-aminothiadiazole-4-carbothioamide

Interaction studies involving 1,2,3-thiadiazole-4-carbothioamide, 5-amino- focus on its binding affinity with biological targets such as enzymes or receptors. Preliminary studies suggest that the compound may interact effectively with certain proteins involved in disease pathways. Further research is needed to elucidate these interactions and their implications for therapeutic applications.

Biological Activity of 5-aminothiadiazole-4-carbothioamide

Research indicates that compounds similar to 1,2,3-thiadiazole-4-carbothioamide, 5-amino- exhibit significant biological activities. Some potential activities include:

  • Antimicrobial Properties: Thiadiazole derivatives have been studied for their ability to inhibit bacterial growth and show antifungal activity.
  • Anticancer Activity: Certain thiadiazole compounds have demonstrated cytotoxic effects against various cancer cell lines.
  • Anti-inflammatory Effects: Thiadiazoles may also possess anti-inflammatory properties, making them candidates for therapeutic development.

The specific biological activity of 1,2,3-thiadiazole-4-carbothioamide, 5-amino- requires further investigation to establish its efficacy and mechanisms of action.

Retrosynthesis analysis of 5-aminothiadiazole-4-carbothioamide

  • Route#1

    Cas:6944-34-9
    Cas:100097-66-3