Description

1-Azabicyclo[2.2.2]Oct-7-Yl-(3,4-Dihydro-2H-Quinolin-1-Yl)Methanone is a sophisticated bicyclic organic compound featuring a quinoline-derived moiety, serving as a critical advanced pharmaceutical intermediate and key building block in medicinal chemistry. Its unique fused-ring structure makes it highly valuable for the synthesis of complex molecules targeting the central nervous system. This product is essential for R&D and production teams in the pharmaceutical and fine chemical industries, particularly those developing novel therapeutic agents.

Application

• Pharmaceutical Intermediate: A key precursor in the synthesis of active pharmaceutical ingredients (APIs) with potential neurological activity.
• Medicinal Chemistry Research: Used as a core scaffold or building block for designing and optimizing new drug candidates in high-throughput screening libraries.
• Ligand Synthesis: Employed in the development of complex ligands for biological targets, including receptors and enzymes.
• Fine Chemical Synthesis: Utilized in multi-step organic synthesis to construct complex heterocyclic frameworks for specialty chemicals.
• Academic & Industrial R&D: Serves as a valuable reagent for exploratory research in synthetic organic chemistry and pharmacology.

Basic Information

Product Name	1-Azabicyclo[2.2.2]Oct-7-Yl-(3,4-Dihydro-2H-Quinolin-1-Yl)Methanone
CAS No.	69907-18-2
Molecular Formula	C₁₇H₂₀N₂O
Molecular Weight	268.36 g/mol
Synonyms	7-(3,4-Dihydro-2H-quinolin-1-ylcarbonyl)-1-azabicyclo[2.2.2]octane; 1-Azabicyclo[2.2.2]octan-7-yl(3,4-dihydro-2H-quinolin-1-yl)methanone; 1-(1-Azabicyclo[2.2.2]oct-7-ylcarbonyl)-1,2,3,4-tetrahydroquinoline; 7-(1,2,3,4-Tetrahydroquinoline-1-carbonyl)-1-azabicyclo[2.2.2]octane; Quinoline-1-carboxylic acid, 3,4-dihydro-, 1-azabicyclo[2.2.2]oct-7-yl ester
EINECS	Contact for details

Quality Control

Our 1-Azabicyclo[2.2.2]Oct-7-Yl-(3,4-Dihydro-2H-Quinolin-1-Yl)Methanone is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC and NMR, to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing all critical specifications. Our quality commitment supports compliance with cGMP and ISO standards for pharmaceutical 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 (15-25°C). Keep the container tightly sealed in a dry environment to minimize exposure to moisture.

Specification

Item	Specification
Appearance	White to off-white 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.