Description

2-Carbomethoxy-1H-pyrrolo(3,2-h)quinoline (CAS No. 146724-32-5) is a high-purity heterocyclic organic compound with the molecular formula C₁₃H₁₀N₂O₂. This advanced intermediate, also known by its IUPAC name methyl 1H-pyrrolo[3,2-h]quinoline-2-carboxylate, features a fused pyrroloquinoline scaffold with a reactive carbomethoxy group at the 2-position. Our product is synthesized under strict quality control to ensure >98% purity (HPLC), making it ideal for pharmaceutical research, material science applications, and as a building block for complex nitrogen-containing architectures. The compound is supplied as a crystalline solid with full spectroscopic characterization data (1H NMR, 13C NMR, LC-MS) and is packaged under inert atmosphere to ensure stability. Suitable for use in medicinal chemistry, fluorescence studies, and as a ligand precursor in coordination chemistry.

Properties

• CAS Number: 146724-32-5
• Complexity: 308
• IUPAC Name: methyl 1H-pyrrolo[3,2-h]quinoline-2-carboxylate
• InChI: InChI=1S/C13H10N2O2/c1-17-13(16)10-7-9-5-4-8-3-2-6-14-11(8)12(9)15-10/h2-7,15H,1H3
• InChI Key: GEODGDMMLTYIFV-UHFFFAOYSA-N
• Exact Mass: 226.074227566
• Molecular Formula: C13H10N2O2
• Molecular Weight: 226.23
• SMILES: COC(=O)C1=CC2=C(N1)C3=C(C=CC=N3)C=C2
• Topological: 55
• Monoisotopic Mass: 226.074227566
• Synonyms: methyl 1H-pyrrolo[3,2-h]quinoline-2-carboxylate, 146724-32-5, 2-Carbomethoxy-1H-pyrrolo(3,2-h)quinoline, CCRIS 6308, THF465XGP6, DTXSID80163460, METHYL 1H-PYRROLO(3,2-H)QUINOLINE-2-CARBOXYLATE, 1H-PYRROLO(3,2-H)QUINOLINE-2-CARBOXYLIC ACID, METHYL ESTER, 2-CARBOMETHOXY-1H-PYRROLO[3,2-H]QUINOLINE, DTXCID0085951, UNII-THF465XGP6, Methyl1H-pyrrolo[3,2-h]quinoline-2-carboxylate, DB-213748

Application

This compound serves as a key synthetic intermediate in the development of novel quinoline-based pharmaceuticals, particularly for antimalarial and anticancer research. Its fused heterocyclic structure makes it valuable for studying DNA intercalation mechanisms. Researchers utilize this building block in the synthesis of fluorescent probes due to its extended π-conjugation system. The carbomethoxy group provides an excellent handle for further functionalization through hydrolysis or nucleophilic substitution reactions.

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