structure of Ethyl 3-Bromo-5-chloroimidazo[1,2-a]pyridine-2-carboxylate

Ethyl 3-Bromo-5-chloroimidazo[1,2-a]pyridine-2-carboxylate

CAS No.: 1000018-03-0
M. Wt: 303.540
M. Fa: C10H8BrClN2O2
InChI Key: WQUIGFCTOQNRJA-UHFFFAOYSA-N

Names and Identifiers of 1000018-03-0

CAS Number

1000018-03-0

MDL Number

MFCD09864799

IUPAC Name

ethyl 3-bromo-5-chloroimidazo[1,2-a]pyridine-2-carboxylate

InChI

InChI=1S/C10H8BrClN2O2/c1-2-16-10(15)8-9(11)14-6(12)4-3-5-7(14)13-8/h3-5H,2H2,1H3

InChIKey

WQUIGFCTOQNRJA-UHFFFAOYSA-N

Canonical SMILES

CCOC(=O)C1=C(N2C(=N1)C=CC=C2Cl)Br

UNSPSC Code

12352100

Physical and chemical properties of 1000018-03-0

Density

1.7±0.1 g/cm3

Exact Mass

301.945770

Index of Refraction

1.653

LogP

3.60

Molecular Formula

C10H8BrClN2O2

Molecular Weight

303.540

Safety Information of 1000018-03-0

Pictograms

Signal Word

 Warning

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

Applications of 1000018-03-0

Ethyl 3-Bromo-5-chloroimidazo[1,2-a]pyridine-2-carboxylate is primarily explored for its potential pharmaceutical applications. It may serve as a precursor for developing new drugs targeting various diseases due to its biological activity. Additionally, it could be utilized in material science for creating functionalized polymers or coatings.

Interaction Studies of 1000018-03-0

Studies on Ethyl 3-Bromo-5-chloroimidazo[1,2-a]pyridine-2-carboxylate have focused on its interactions with biomolecules:

  • Enzyme Inhibition: Research has indicated that this compound can inhibit specific enzymes relevant to disease pathways.
  • Binding Affinity: Investigations into its binding affinity with DNA or proteins have shown promise for therapeutic applications.

These interaction studies are crucial for understanding how this compound may function in biological systems and its potential as a drug candidate.

Biological Activity of 1000018-03-0

Research indicates that compounds similar to Ethyl 3-Bromo-5-chloroimidazo[1,2-a]pyridine-2-carboxylate exhibit various biological activities, including antimicrobial, antifungal, and anticancer properties. Specific studies have shown that imidazo-pyridine derivatives can inhibit certain enzymes or interact with DNA, suggesting potential as therapeutic agents.