structure of 7-Methyl-1H-pyrrolo[3,2-c]pyridine-3-carboxylic acid

7-Methyl-1H-pyrrolo[3,2-c]pyridine-3-carboxylic acid

CAS No.: 1000341-52-5
M. Wt: 176.172
M. Fa: C9H8N2O2
InChI Key: UOORYHKUOBPHCI-UHFFFAOYSA-N

Names and Identifiers of 1000341-52-5

CAS Number

1000341-52-5

IUPAC Name

7-methyl-1H-pyrrolo[3,2-c]pyridine-3-carboxylic acid

InChI

InChI=1S/C9H8N2O2/c1-5-2-10-3-6-7(9(12)13)4-11-8(5)6/h2-4,11H,1H3,(H,12,13)

InChIKey

UOORYHKUOBPHCI-UHFFFAOYSA-N

Canonical SMILES

CC1=CN=CC2=C1NC=C2C(=O)O

Physical and chemical properties of 1000341-52-5

Boiling Point

460.6±40.0 °C at 760 mmHg

Density

1.4±0.1 g/cm3

Exact Mass

176.058578

Flash Point

232.4±27.3 °C

Index of Refraction

1.709

LogP

0.96

Molecular Formula

C9H8N2O2

Molecular Weight

176.172

PSA

65.98000

Vapour Pressure

0.0±1.2 mmHg at 25°C

Safety Information of 1000341-52-5

Pictograms

Signal Word

 Warning

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

Applications of 1000341-52-5

7-Methyl-1H-pyrrolo[3,2-c]pyridine-3-carboxylic acid has several applications across different fields:

  • Chemistry: Serves as a building block in synthesizing more complex molecules.
  • Biology: Under investigation for its potential as an antimicrobial and anticancer agent.
  • Medicine: Explored for its role in drug development targeting specific enzymes or receptors.
  • Industry: Potentially useful in developing new materials with unique electronic or optical properties.

Interaction Studies of 1000341-52-5

The mechanism of action for 7-Methyl-1H-pyrrolo[3,2-c]pyridine-3-carboxylic acid involves binding to specific molecular targets, which may inhibit enzyme activity by blocking their active sites. Such interactions are critical in understanding its biological effects and therapeutic potential. Ongoing studies aim to elucidate these mechanisms further to optimize its use in medicinal chemistry.

Biological Activity of 1000341-52-5

Research indicates that 7-Methyl-1H-pyrrolo[3,2-c]pyridine-3-carboxylic acid exhibits potential biological activities. It has been studied for its antimicrobial and anticancer properties. The compound may act by inhibiting specific enzymes or receptors, thus blocking critical pathways in cellular processes. Its interaction with biological targets suggests it could be a candidate for further drug development aimed at treating various diseases.