structure of 6-Bromoimidazo[1,2-a]pyrazine-2-carboxylic acid

6-Bromoimidazo[1,2-a]pyrazine-2-carboxylic acid

CAS No.: 1000018-56-3
M. Wt: 242.030
M. Fa: C7H4BrN3O2
InChI Key: KEMAWFHELKESRS-UHFFFAOYSA-N
Appearance: Pale-yellow Solid

Names and Identifiers of 1000018-56-3

CAS Number

1000018-56-3

EC Number

802-303-0

MDL Number

MFCD09414724

IUPAC Name

6-bromoimidazo[1,2-a]pyrazine-2-carboxylic acid

InChI

InChI=1S/C7H4BrN3O2/c8-5-3-11-2-4(7(12)13)10-6(11)1-9-5/h1-3H,(H,12,13)

InChIKey

KEMAWFHELKESRS-UHFFFAOYSA-N

Canonical SMILES

C1=C(N=C2N1C=C(N=C2)Br)C(=O)O

UNSPSC Code

12352100

Physical and chemical properties of 1000018-56-3

Acidity coefficient

3.13±0.30(Predicted)

Density

2.1±0.1 g/cm3

Exact Mass

240.948685

Index of Refraction

1.792

LogP

0.73

Molecular Formula

C7H4BrN3O2

Molecular Weight

242.030

PSA

67.49000

Storage condition

2-8°C

Water Solubility

Sparingly soluble (15 g/L) (25 ºC)

Safety Information of 1000018-56-3

Pictograms

Signal Word

 Warning

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

Applications of 1000018-56-3

6-Bromoimidazo[1,2-a]pyrazine-2-carboxylic acid has several applications in various fields:

  • Pharmaceutical Development: Its unique structure makes it a candidate for drug development targeting specific diseases.
  • Biochemical Research: It serves as a valuable tool in proteomics and enzyme inhibition studies.
  • Agricultural Chemistry: Potential applications in developing agrochemicals due to its biological activity against pathogens.

Interaction Studies of 1000018-56-3

Interaction studies have focused on understanding how 6-Bromoimidazo[1,2-a]pyrazine-2-carboxylic acid interacts with biological macromolecules:

  • Protein Binding: Investigations into how this compound binds to proteins can provide insights into its mechanism of action.
  • Receptor Interactions: Studies have explored its affinity for various receptors, which is crucial for assessing its pharmacological properties.
  • Metabolic Pathways: Understanding its metabolism can help predict efficacy and safety profiles in therapeutic contexts.

Biological Activity of 1000018-56-3

Research indicates that 6-Bromoimidazo[1,2-a]pyrazine-2-carboxylic acid exhibits significant biological activities, including:

  • Antimicrobial Properties: Studies have shown that this compound possesses antimicrobial effects against various strains of bacteria and fungi.
  • Anticancer Activity: Preliminary investigations suggest potential cytotoxic effects against cancer cell lines, indicating its promise as an anticancer agent.
  • Enzyme Inhibition: The compound has been evaluated for its ability to inhibit specific enzymes, which may relate to its therapeutic potential in various diseases.

Physical sample testing spectrum (NMR) of 1000018-56-3

Physical sample testing spectrum (NMR) of 1000018-56-3