Description

5,6,7,8,9,10-Hexahydro-2-Chloro-11H-Cyclohepta[B]Quinolin-11-One is a high-purity, advanced pharmaceutical intermediate with a complex fused-ring structure. This compound is valued for its role as a critical building block in the synthesis of novel active pharmaceutical ingredients (APIs) and fine chemicals. It is primarily sought by research institutions and manufacturers in the pharmaceutical, agrochemical, and specialty chemical industries for developing new therapeutic agents and high-value compounds.

Application

• Pharmaceutical Intermediate: A key precursor in the synthesis of complex heterocyclic compounds and potential drug candidates.
• Agrochemical Research: Used in the development of new pesticides and herbicides due to its bioactive quinoline core.
• Organic Synthesis Building Block: Serves as a versatile scaffold for constructing more complex molecular architectures in medicinal and process chemistry.
• Material Science Research: Investigated for potential applications in creating organic electronic materials or specialty polymers.
• Academic & R&D: Utilized in university and corporate research laboratories for method development and exploratory chemistry.

Basic Information

Product Name	5,6,7,8,9,10-Hexahydro-2-Chloro-11H-Cyclohepta[B]Quinolin-11-One
CAS No.	5778-57-4
Molecular Formula	C15H14ClNO
Molecular Weight	259.73 g/mol
Synonyms	2-Chloro-5,6,7,8,9,10-hexahydrocyclohepta[b]quinolin-11-one; 2-Chloro-5,6,7,8,9,10-hexahydrocyclohepta[b]quinolin-11(11H)-one; 2-Chloro-11H-cyclohepta[b]quinolin-11-one, 5,6,7,8,9,10-hexahydro-; 2-Chloro-5,6,7,8,9,10-hexahydrocyclohepta[b]quinolin-11(11H)-on; Cyclohepta[b]quinolin-11-one, 2-chloro-5,6,7,8,9,10-hexahydro-
EINECS	Contact for details

Quality Control

Our 5,6,7,8,9,10-Hexahydro-2-Chloro-11H-Cyclohepta[B]Quinolin-11-One is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with every shipment, detailing all critical specifications. Our quality commitment supports compliance with cGMP and ICH guidelines for pharmaceutical intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Keep away from incompatible materials such as strong oxidizing agents. For long-term storage, consider an inert atmosphere to maintain product integrity.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 98.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
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.