Description

Methyl 1H-Pyrrolo[3,2-H]Quinoline-2-Carboxylate is a high-purity, advanced pharmaceutical intermediate with a complex fused heterocyclic structure. This compound is valued for its role as a critical building block in the synthesis of novel active pharmaceutical ingredients (APIs), particularly in therapeutic areas requiring sophisticated molecular scaffolds. It is primarily utilized by research institutions and pharmaceutical manufacturers engaged in the development of new drug candidates, especially within oncology and antiviral research. The material is supplied with stringent quality control to ensure batch-to-batch consistency for sensitive synthetic pathways.

Application

• Pharmaceutical Intermediate: A key precursor in the multi-step synthesis of complex drug molecules and investigational new drugs.
• Organic Synthesis Building Block: Used in research and development for constructing novel pyrroloquinoline-based heterocyclic compounds.
• Medicinal Chemistry Research: Serves as a core scaffold for structure-activity relationship (SAR) studies in drug discovery programs.
• Agrochemical Intermediate: Potential use in the development of new crop protection agents with specific biological activity.
• Material Science Research: Investigated for use in the development of organic electronic materials due to its conjugated system.

Basic Information

Product Name	Methyl 1H-Pyrrolo[3,2-H]Quinoline-2-Carboxylate
CAS No.	146724-32-5
Molecular Formula	C13H10N2O2
Molecular Weight	226.23 g/mol
Synonyms	Methyl 1H-pyrrolo[3,2-h]quinoline-2-carboxylate; 1H-Pyrrolo[3,2-h]quinoline-2-carboxylic acid, methyl ester; Methyl pyrroloquinoline-2-carboxylate; 146724-32-5; Methyl 1H-pyrrolo[3,2-h]quinoline-2-carboxylate; Pyrrolo[3,2-h]quinoline-2-carboxylic acid methyl ester
EINECS	Contact for details

Quality Control

Our Methyl 1H-Pyrrolo[3,2-H]Quinoline-2-Carboxylate is manufactured under a strict quality management system. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency, meeting the exacting standards required for pharmaceutical R&D. A detailed Certificate of Analysis (COA) is provided with each shipment, documenting key parameters such as assay purity and impurity profiles. We support compliance with relevant guidelines for advanced intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (typically 15-25°C). Keep the container tightly sealed to protect from moisture. Store away from incompatible materials.

Specification

Item	Specification
Appearance	Off-white to light yellow crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Any single impurity	≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 0.5%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.