Description

Ethyl 7-[2-(Morpholinomethyl)Phenyl]-7-Oxoheptanoate is a high-purity synthetic intermediate featuring a morpholine-substituted aromatic ketone ester structure. This compound is valued for its role as a versatile building block in advanced organic synthesis, particularly for constructing complex pharmacologically active molecules. It is primarily sought by research institutions and pharmaceutical development companies engaged in the creation of new chemical entities and active pharmaceutical ingredients (APIs).

Application

• Pharmaceutical Intermediate: A key precursor in the synthesis of novel drug candidates, especially those targeting neurological or inflammatory pathways.
• Chemical Research & Development: Serves as a critical building block for medicinal chemists exploring new molecular scaffolds and structure-activity relationships (SAR).
• Active Pharmaceutical Ingredient (API) Synthesis: Used in multi-step synthetic routes for the production of complex target molecules in pre-clinical and clinical development.
• Custom Synthesis & Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for bespoke synthesis projects requiring high-purity intermediates.
• Reference Standard: Utilized as an analytical standard in quality control laboratories for method development and impurity profiling.

Basic Information

Product Name	Ethyl 7-[2-(Morpholinomethyl)Phenyl]-7-Oxoheptanoate
CAS No.	898751-57-0
Molecular Formula	C20H29NO4
Molecular Weight	347.45 g/mol
Synonyms	Ethyl 7-oxo-7-[2-(morpholin-4-ylmethyl)phenyl]heptanoate; 7-[2-(Morpholinomethyl)phenyl]-7-oxoheptanoic Acid Ethyl Ester; Heptanoic acid, 7-oxo-7-[2-(4-morpholinylmethyl)phenyl]-, ethyl ester; Ethyl 7-oxo-7-[2-(morpholin-4-ylmethyl)phenyl]heptanoate; 898751-57-0
EINECS	Contact for details

Quality Control

Our Ethyl 7-[2-(Morpholinomethyl)Phenyl]-7-Oxoheptanoate is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) detailing specifications such as assay (HPLC), related substances, and residual solvents. Our quality commitment supports compliance with cGMP guidelines 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 area at controlled room temperature (15-25°C). Keep away from strong oxidizing agents and incompatible materials. For long-term storage, consider holding under an inert atmosphere to maintain optimal stability.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
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.