structure of 3-Methylimidazo[1,2-a]pyridine-2-carbaldehyde

3-Methylimidazo[1,2-a]pyridine-2-carbaldehyde

CAS No.: 1001754-85-3
M. Wt: 160.17300
M. Fa: C9H8N2O
InChI Key: PKDTULJSYQPSFW-UHFFFAOYSA-N
Appearance: Yellow-brown Solid

Names and Identifiers of 1001754-85-3

CAS Number

1001754-85-3

MDL Number

MFCD10001441

IUPAC Name

3-methylimidazo[1,2-a]pyridine-2-carbaldehyde

InChI

InChI=1S/C9H8N2O/c1-7-8(6-12)10-9-4-2-3-5-11(7)9/h2-6H,1H3

InChIKey

PKDTULJSYQPSFW-UHFFFAOYSA-N

Canonical SMILES

CC1=C(N=C2N1C=CC=C2)C=O

UNSPSC Code

12352100

Physical and chemical properties of 1001754-85-3

Acidity coefficient

3.88±0.50(Predicted)

Density

1.21±0.1 g/cm3(Predicted)

Exact Mass

160.06400

LogP

1.45520

Molecular Formula

C9H8N2O

Molecular Weight

160.17300

PSA

34.37000

Storage condition

under inert gas (nitrogen or Argon) at 2-8°C

Safety Information of 1001754-85-3

Pictograms

Signal Word

 Warning

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

Applications of 1001754-85-3

3-Methylimidazo[1,2-a]pyridine-2-carbaldehyde has several applications:

  • Medicinal Chemistry: Explored for developing new drugs targeting resistant infections and cancer.
  • Organic Synthesis: Serves as a building block for synthesizing more complex heterocyclic compounds.
  • Material Science: Its unique properties make it suitable for applications in optoelectronic devices and sensors.

Interaction Studies of 1001754-85-3

Studies on the interactions of 3-Methylimidazo[1,2-a]pyridine-2-carbaldehyde with biological systems have shown promising results. The compound's ability to inhibit certain enzymes and interact with DNA suggests potential mechanisms for its antimicrobial and anticancer activities. Ongoing research aims to elucidate these interactions further, providing insights into its mode of action at the molecular level.

Biological Activity of 1001754-85-3

Research indicates that 3-Methylimidazo[1,2-a]pyridine-2-carbaldehyde exhibits significant biological activities. Notably, it has been studied for its antimicrobial properties, particularly against resistant strains of fungi such as Candida albicans. Additionally, its derivatives have shown potential in anticancer research and as agents against multidrug-resistant tuberculosis. The compound's unique structure allows it to interact with biological targets effectively, contributing to its therapeutic potential.

Physical sample testing spectrum (NMR) of 1001754-85-3

Physical sample testing spectrum (NMR) of 1001754-85-3