1H-Pyrrolo[3,2-h]quinoline-2-carboxylic acid


Chemical Name: 1H-Pyrrolo[3,2-h]quinoline-2-carboxylic acid
CAS Number: 58457-37-7
Product Number: AG00EBZH(AGN-PC-0JMWDT)
Synonyms:
MDL No:
Molecular Formula: C12H8N2O2
Molecular Weight: 212.2041

Identification/Properties


Properties
BP:
536.6°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



1H-Pyrrolo[3,2-h]quinoline-2-carboxylic acid, also known as $name$, is widely utilized in chemical synthesis as a versatile building block in the creation of various pharmaceuticals and organic compounds. Due to its unique molecular structure and functional groups, this compound serves as a key intermediate in the synthesis of biologically active molecules.In organic synthesis, $name$ can undergo various reactions such as esterification, amidation, and coupling reactions to introduce different substituents at specific positions on the pyrroloquinoline ring system. This allows chemists to tailor the properties of the final product, making it a valuable tool in medicinal chemistry and drug development.Furthermore, the carboxylic acid group in $name$ can be activated to form reactive intermediates for the formation of peptide bonds or other important linkages. By strategically incorporating 1H-Pyrrolo[3,2-h]quinoline-2-carboxylic acid into synthetic pathways, chemists can access structurally diverse compounds with potential biological activities.Overall, the application of 1H-Pyrrolo[3,2-h]quinoline-2-carboxylic acid in chemical synthesis enables researchers to design and prepare novel molecules with tailored properties, making it a pivotal component in the development of new drugs and materials.