Description

(4-Chloro-1-Methyl-1H-Pyrrolo[3,2-C]Pyridin-3-Yl)Methanol is a high-purity, advanced pharmaceutical intermediate belonging to the fused pyrrolopyridine class of heterocyclic compounds. This compound is critical for the research and development of novel small-molecule therapeutics, particularly in oncology and central nervous system (CNS) drug discovery. It is primarily utilized by pharmaceutical R&D laboratories, contract research organizations (CROs), and fine chemical manufacturers engaged in the synthesis of targeted, high-value active pharmaceutical ingredients (APIs).

Application

• Pharmaceutical Intermediate: Serves as a key building block in the synthesis of complex drug candidates targeting specific biological pathways.
• Kinase Inhibitor Development: Used in the research and production of protein kinase inhibitors for cancer therapy, leveraging its privileged heterocyclic scaffold.
• Medicinal Chemistry Research: Provides a versatile core structure for structure-activity relationship (SAR) studies and lead optimization in drug discovery programs.
• API Synthesis: Employed in multi-step synthetic routes for the manufacture of preclinical and clinical trial materials.
• Biochemical Tool Compound: Acts as a precursor for labeled probes or analogs used in biochemical and pharmacological assays.
• Custom Synthesis Projects: Supplied to fine chemical companies for bespoke synthesis and scale-up services for their clients.

Basic Information

Product Name	(4-Chloro-1-Methyl-1H-Pyrrolo[3,2-C]Pyridin-3-Yl)Methanol
CAS No.	97989-54-3
Molecular Formula	C9H9ClN2O
Molecular Weight	196.63 g/mol
Synonyms	4-Chloro-1-methyl-1H-pyrrolo[3,2-c]pyridine-3-methanol; 3-(Hydroxymethyl)-4-chloro-1-methyl-1H-pyrrolo[3,2-c]pyridine; 1-Methyl-4-chloro-1H-pyrrolo[3,2-c]pyridine-3-methanol; (4-Chloro-1-methyl-1H-pyrrolo[3,2-c]pyridin-3-yl)methanol; 97989-54-3; 4-Chloro-1-methyl-pyrrolo[3,2-c]pyridine-3-methanol
EINECS	Contact for details

Quality Control

Our production of (4-Chloro-1-Methyl-1H-Pyrrolo[3,2-C]Pyridin-3-Yl)Methanol adheres to stringent quality management protocols to ensure batch-to-batch consistency and high purity, essential for sensitive pharmaceutical applications. All materials are subjected to rigorous analytical testing, including HPLC, NMR, and MS, to confirm identity, purity, and the absence of critical impurities. A comprehensive Certificate of Analysis (COA) detailing all specifications is provided with each shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). This compound may be moisture-sensitive; keep the container tightly sealed under an inert atmosphere if specified. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Single Unknown Impurity (HPLC)	≤ 0.5%
Total Impurities (HPLC)	≤ 2.0%

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