structure of 4-Methyl-1H-pyrrolo[3,2-c]pyridine-3-carboxylic acid

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

CAS No.: 1000342-75-5
M. Wt: 176.172
M. Fa: C9H8N2O2
InChI Key: WWCLXULQDPMSPV-UHFFFAOYSA-N

Names and Identifiers of 1000342-75-5

CAS Number

1000342-75-5

MDL Number

MFCD09749965

IUPAC Name

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

InChI

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

InChIKey

WWCLXULQDPMSPV-UHFFFAOYSA-N

Canonical SMILES

CC1=NC=CC2=C1C(=CN2)C(=O)O

UNSPSC Code

12352100

Physical and chemical properties of 1000342-75-5

Boiling Point

445.8±40.0 °C at 760 mmHg

Density

1.4±0.1 g/cm3

Exact Mass

176.058578

Flash Point

223.4±27.3 °C

H Bond Acceptors

3

H Bond Donors

2

Index of Refraction

1.709

LogP

0.96

Molecular Formula

C9H8N2O2

Molecular Weight

176.172

PSA

65.98000

Vapour Pressure

0.0±1.1 mmHg at 25°C

Safety Information of 1000342-75-5

Pictograms

Signal Word

 Warning

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

Applications of 1000342-75-5

The applications of 4-Methyl-1H-pyrrolo[3,2-c]pyridine-3-carboxylic acid span various fields:

  • Pharmaceuticals: Its derivatives are being explored for potential therapeutic applications due to their biological activities.
  • Agricultural Chemicals: Compounds with similar structures may be utilized as agrochemicals due to their antimicrobial properties.
  • Material Science: The unique structural characteristics allow for potential use in developing novel materials with specific properties.

Biological Activity of 1000342-75-5

4-Methyl-1H-pyrrolo[3,2-c]pyridine-3-carboxylic acid has been studied for its potential biological activities:

  • Antimicrobial Properties: Some derivatives exhibit activity against various bacteria and fungi.
  • Cytotoxicity: Research indicates that certain structural modifications can enhance cytotoxic effects on cancer cell lines.
  • Enzyme Inhibition: The compound may act as an inhibitor for specific enzymes, although detailed studies are necessary to elucidate these mechanisms.