structure of Ethyl 6,8-difluoroimidazo[1,2-A]pyridine-2-carboxylate

Ethyl 6,8-difluoroimidazo[1,2-A]pyridine-2-carboxylate

CAS No.: 1000844-18-7
M. Wt: 226.180
M. Fa: C10H8F2N2O2
InChI Key: QLLNOXBPJKXPAQ-UHFFFAOYSA-N

Names and Identifiers of 1000844-18-7

CAS Number

1000844-18-7

MDL Number

MFCD22631475

IUPAC Name

ethyl 6,8-difluoroimidazo[1,2-a]pyridine-2-carboxylate

InChI

InChI=1S/C10H8F2N2O2/c1-2-16-10(15)8-5-14-4-6(11)3-7(12)9(14)13-8/h3-5H,2H2,1H3

InChIKey

QLLNOXBPJKXPAQ-UHFFFAOYSA-N

Canonical SMILES

CCOC(=O)C1=CN2C=C(C=C(C2=N1)F)F

UNSPSC Code

12352100

Physical and chemical properties of 1000844-18-7

Density

1.4±0.1 g/cm3

Exact Mass

226.055389

Index of Refraction

1.564

LogP

2.49

Molecular Formula

C10H8F2N2O2

Molecular Weight

226.180

PSA

43.60000

Storage condition

Sealed in dry,Room Temperature

Safety Information of 1000844-18-7

Pictograms

Signal Word

 Warning

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

Applications of 1000844-18-7

Ethyl 6,8-difluoroimidazo[1,2-a]pyridine-2-carboxylate has potential applications in:

  • Pharmaceutical Development: Its unique structure may lead to the discovery of new drugs targeting bacterial infections or cancer.
  • Chemical Research: As a building block in organic synthesis, it can be used to create more complex molecules with desired biological activities.
  • Material Science: Its properties may be explored for use in developing new materials or coatings.

Interaction Studies of 1000844-18-7

Interaction studies involving ethyl 6,8-difluoroimidazo[1,2-a]pyridine-2-carboxylate often focus on its binding affinity to specific biological targets. These studies help elucidate its mechanism of action and potential therapeutic uses. Techniques such as molecular docking simulations and biochemical assays are commonly employed to assess these interactions.

Biological Activity of 1000844-18-7

Compounds related to ethyl 6,8-difluoroimidazo[1,2-a]pyridine-2-carboxylate have shown promising biological activities. They may exhibit antibacterial properties by inhibiting bacterial cell division through interaction with the ftsZ protein, a crucial component of the bacterial cytoskeleton. Additionally, related compounds have been studied for their potential in treating various conditions, including cancer and inflammation.