Description

1-(3,4-Dichlorophenyl)-4-Oxocyclohexanecarboxylic Acid is a high-purity, synthetically derived organic compound with the CAS registry number 773101-05-6. This advanced pharmaceutical intermediate is valued for its precise chemical structure, which serves as a critical building block in the synthesis of complex active pharmaceutical ingredients (APIs). It is essential for research and development chemists and manufacturers in the pharmaceutical and agrochemical industries seeking reliable, high-quality intermediates for their synthesis pathways.

Application

This specialized intermediate is designed for high-value synthesis applications. Its primary and potential uses include:

• Pharmaceutical Intermediate: A key precursor in the research and synthesis of novel drug candidates, particularly in central nervous system (CNS) and metabolic disorder therapeutic areas.
• Agrochemical Synthesis: Used in the development of advanced herbicides and pesticides, leveraging the dichlorophenyl moiety for biological activity.
• Chemical Research & Development: Serves as a versatile scaffold in medicinal chemistry for structure-activity relationship (SAR) studies and lead optimization.
• Custom Synthesis: Employed by contract research and manufacturing organizations (CROs/CMOs) for bespoke chemical synthesis projects.
• Academic Research: Utilized in university and institutional labs for studying organic reaction mechanisms and developing new synthetic methodologies.

Basic Information

Product Name	1-(3,4-Dichlorophenyl)-4-Oxocyclohexanecarboxylic Acid
CAS No.	773101-05-6
Molecular Formula	C13H12Cl2O3
Molecular Weight	287.14 g/mol
Synonyms	4-Oxo-1-(3,4-dichlorophenyl)cyclohexanecarboxylic acid; 1-(3,4-Dichlorophenyl)-4-oxocyclohexanecarboxylic acid; Cyclohexanecarboxylic acid, 1-(3,4-dichlorophenyl)-4-oxo-; 773101-05-6; 4-Oxo-1-(3,4-dichlorophenyl)cyclohexane-1-carboxylic acid
EINECS	Contact for details

Quality Control

Our production of 1-(3,4-Dichlorophenyl)-4-Oxocyclohexanecarboxylic Acid adheres to stringent quality management protocols. Every batch undergoes comprehensive analytical testing, including HPLC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. We provide a detailed Certificate of Analysis (COA) with each shipment, documenting all critical quality attributes. Our quality system is designed to meet the rigorous standards required for pharmaceutical intermediate applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). Keep away from strong oxidizing agents, strong bases, and sources of ignition. For long-term storage, consider inert atmosphere conditions to maintain optimal purity.

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.