Description

Ethyl 2-[8-(4-Chlorophenyl)-10-Oxa-7-Azabicyclo[4.4.0]Deca-2,4,7,11-Te Traen-4-Yl]Acetate is a high-purity, advanced pharmaceutical intermediate characterized by its complex bicyclic heterocyclic structure. This compound is of significant value for its role as a key building block in the synthesis of novel active pharmaceutical ingredients (APIs), particularly in therapeutic areas requiring sophisticated molecular architectures. It is primarily sought by research institutions and manufacturers in the pharmaceutical and agrochemical sectors for process development and scale-up activities.

Application

• Pharmaceutical Intermediate: A critical precursor in the research and synthesis of new drug candidates, especially for central nervous system (CNS) or anti-inflammatory targets.
• Agrochemical Research: Serves as a structural motif in developing new generation pesticides and herbicides with specific activity profiles.
• Organic Synthesis Building Block: Used in academic and industrial R&D for constructing complex heterocyclic compounds and exploring novel chemical spaces.
• Process Chemistry Development: Employed in route scouting and optimization studies for the efficient, scalable production of target molecules.
• Reference Standard: Utilized as an analytical standard for quality control and method validation in API manufacturing.

Basic Information

Product Name	Ethyl 2-[8-(4-Chlorophenyl)-10-Oxa-7-Azabicyclo[4.4.0]Deca-2,4,7,11-Te Traen-4-Yl]Acetate
CAS No.	86818-20-4
Molecular Formula	C21H20ClNO3
Molecular Weight	369.84 g/mol
Synonyms	Ethyl 2-[8-(4-chlorophenyl)-10-oxa-7-azabicyclo[4.4.0]deca-2,4,7,11-tetraen-4-yl]acetate; 86818-20-4; 10-Oxa-7-azabicyclo[4.4.0]deca-2,4,7,11-tetraene-4-acetic acid, 8-(4-chlorophenyl)-, ethyl ester; Ethyl 8-(4-chlorophenyl)-10-oxa-7-azabicyclo[4.4.0]deca-2,4,7,11-tetraene-4-acetate
EINECS	Contact for details

Quality Control

Our Ethyl 2-[8-(4-Chlorophenyl)-10-Oxa-7-Azabicyclo[4.4.0]Deca-2,4,7,11-Te Traen-4-Yl]Acetate is manufactured under strict quality management systems. Every batch undergoes rigorous analytical testing, including HPLC for purity and identity confirmation, to ensure it meets the stringent requirements for pharmaceutical intermediate applications. A comprehensive Certificate of Analysis (COA) detailing all specifications and test results is provided with each shipment.

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). The container should be kept tightly sealed to protect against moisture. 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%
Loss on Drying	≤ 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.