Description

Methyl 1-(3-Chlorophenyl)-4-Oxocyclohexanecarboxylate is a high-purity, synthetically valuable cyclohexanone derivative. This compound serves as a critical advanced pharmaceutical intermediate (API) and a versatile building block in organic synthesis. It is primarily required by R&D chemists and process development teams in the pharmaceutical, agrochemical, and fine chemical industries for the development of novel active compounds.

Application

• Pharmaceutical Intermediate: Key precursor in the synthesis of complex drug molecules, particularly those targeting central nervous system (CNS) disorders.
• Agrochemical Research: Used as a building block for developing new herbicides, fungicides, and plant growth regulators.
• Organic Synthesis: Versatile synthon for constructing complex polycyclic structures via reactions like Michael additions, alkylations, and cyclizations.
• Material Science Research: Potential monomer or modifier in the development of specialty polymers with unique thermal or optical properties.
• Academic & Contract Research: Essential for methodological studies and discovery chemistry in university and CRO (Contract Research Organization) laboratories.

Basic Information

Product Name	Methyl 1-(3-Chlorophenyl)-4-Oxocyclohexanecarboxylate
CAS No.	1384264-35-0
Molecular Formula	C14H15ClO3
Molecular Weight	266.72 g/mol
Synonyms	Methyl 1-(3-chlorophenyl)-4-oxocyclohexanecarboxylate; 4-Oxo-1-(3-chlorophenyl)cyclohexanecarboxylic acid methyl ester; 1-(3-Chlorophenyl)-4-oxocyclohexanecarboxylic acid methyl ester; Methyl 4-oxo-1-(m-chlorophenyl)cyclohexanecarboxylate; 1384264-35-0; Cyclohexanecarboxylic acid, 1-(3-chlorophenyl)-4-oxo-, methyl ester
EINECS	Contact for details

Quality Control

Our production of Methyl 1-(3-Chlorophenyl)-4-Oxocyclohexanecarboxylate adheres to stringent in-process controls and final release testing to ensure batch-to-batch consistency and high purity. Quality is verified against comprehensive specifications using advanced analytical techniques including HPLC, GC, and NMR. A Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with each shipment. We support cGMP compliance for pharmaceutical applications.

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 away from strong oxidizing agents and bases. 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
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Any single unknown impurity	≤ 0.5%
Residual Solvents (GC)	Meets 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.