structure of 3,4-Dibromo-1H-pyrrolo[3,2-c]pyridine

3,4-Dibromo-1H-pyrrolo[3,2-c]pyridine

CAS No.: 1000341-83-2
M. Wt: 275.928
M. Fa: C7H4Br2N2
InChI Key: XLYNOUQRLSJSII-UHFFFAOYSA-N

Names and Identifiers of 3,4-Dibromo-1H-pyrrolo[3,2-c]pyridine

CAS Number

1000341-83-2

IUPAC Name

3,4-dibromo-1H-pyrrolo[3,2-c]pyridine

InChI

InChI=1S/C7H4Br2N2/c8-4-3-11-5-1-2-10-7(9)6(4)5/h1-3,11H

InChIKey

XLYNOUQRLSJSII-UHFFFAOYSA-N

Canonical SMILES

C1=CN=C(C2=C1NC=C2Br)Br

Physical and chemical properties of 3,4-Dibromo-1H-pyrrolo[3,2-c]pyridine

Boiling Point

417.3±40.0 °C at 760 mmHg

Density

2.2±0.1 g/cm3

Exact Mass

273.874115

Flash Point

206.2±27.3 °C

Index of Refraction

1.751

LogP

2.23

Molecular Formula

C7H4Br2N2

Molecular Weight

275.928

PSA

28.68000

Vapour Pressure

0.0±0.9 mmHg at 25°C

Applications of 3,4-Dibromo-1H-pyrrolo[3,2-c]pyridine

3,4-Dibromo-1H-pyrrolo[3,2-c]pyridine has several applications in different fields:

  • Pharmaceutical Development: Its derivatives are being explored as potential drugs due to their biological activities.
  • Material Science: The compound's unique properties may be utilized in developing new materials with specific electronic or optical characteristics.
  • Chemical Research: As a versatile intermediate, it serves as a building block for synthesizing other complex organic compounds .

Interaction Studies of 3,4-Dibromo-1H-pyrrolo[3,2-c]pyridine

Interaction studies involving 3,4-dibromo-1H-pyrrolo[3,2-c]pyridine often focus on its binding affinity with various biological targets. These studies help elucidate its mechanism of action and potential therapeutic effects. For instance:

  • Protein-Ligand Interactions: Investigations into how this compound interacts with specific proteins involved in disease pathways provide insights into its potential as a drug candidate.
  • Cellular Mechanisms: Understanding how it influences cellular processes can reveal its role in modulating biological functions .

Biological Activity of 3,4-Dibromo-1H-pyrrolo[3,2-c]pyridine

3,4-Dibromo-1H-pyrrolo[3,2-c]pyridine exhibits significant biological activities. Compounds in the pyrrolo[3,2-c]pyridine family have been studied for their potential as:

  • Antitumor Agents: Some derivatives show promise in inhibiting tumor growth by targeting specific cancer pathways.
  • Antimicrobial Activity: Research indicates that related compounds may possess antibacterial properties against various pathogens.
  • Neuroprotective Effects: Certain derivatives have been evaluated for their ability to protect neuronal cells from damage.

Studies suggest that the unique structure of 3,4-dibromo-1H-pyrrolo[3,2-c]pyridine contributes to its biological efficacy .