Description

Ethyl 1-(2,3-Diethyl-6-Quinoxalinyl)-4-Piperidinecarboxylate is a high-purity, advanced pharmaceutical intermediate belonging to the quinoxaline class of heterocyclic compounds. This compound matters for its role as a critical building block in the synthesis of novel active pharmaceutical ingredients (APIs), particularly those targeting central nervous system (CNS) disorders. Pharmaceutical R&D teams and fine chemical manufacturers need it to develop new therapeutic agents, leveraging its complex molecular scaffold to create potent and selective drug candidates.

Application

• Pharmaceutical Intermediate: A key precursor in the multi-step synthesis of novel drug candidates, especially in neurological and psychiatric research.
• Chemical Biology Research: Used as a molecular probe or scaffold in medicinal chemistry for structure-activity relationship (SAR) studies.
• API Development: Serves as a core structural component in the development of new Active Pharmaceutical Ingredients (APIs).
• Contract Research & Manufacturing (CRO/CMO): Supplied to organizations specializing in custom synthesis and process development for the pharmaceutical industry.
• Academic Research: Utilized in university and institutional labs for investigating new heterocyclic chemistry and potential therapeutic pathways.

Basic Information

Item	Details
Product Name	Ethyl 1-(2,3-Diethyl-6-Quinoxalinyl)-4-Piperidinecarboxylate
CAS No.	439095-56-4
Molecular Formula	C20H27N3O2
Molecular Weight	341.45 g/mol
Synonyms	1-(2,3-Diethylquinoxalin-6-yl)-4-piperidinecarboxylic acid ethyl ester; Ethyl 4-[1-(2,3-diethylquinoxalin-6-yl)]piperidine-1-carboxylate; 4-Piperidinecarboxylic acid, 1-(2,3-diethyl-6-quinoxalinyl)-, ethyl ester; UNII-8H5J6V4E6S; 8H5J6V4E6S; Ethyl 1-(2,3-diethylquinoxalin-6-yl)piperidine-4-carboxylate; AOB6777; BDBM50111671
EINECS	Contact for details

Quality Control

Our Ethyl 1-(2,3-Diethyl-6-Quinoxalinyl)-4-Piperidinecarboxylate is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing all specification results. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliability for your critical R&D and scale-up processes.

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 away from incompatible materials. For long-term storage, consider an inert atmosphere to maintain optimal stability.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (HPLC)	Conforms
Identification (IR)	Conforms
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Water Content (KF)	≤ 0.5%
Heavy Metals	≤ 20 ppm

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