6966-15-0

Basic information

• Product Name: 2-(4-methoxybenzoyl)cyclohexanecarboxylic acid
• Synonyms: 2-(4-Methoxybenzoyl)cyclohexanecarboxylic acid; Cyclohexanecarboxylic acid, 2-(4-methoxybenzoyl)-
• CAS NO: 6966-15-0
• Molecular Formula: C₁₅H₁₈O₄
• Molecular Weight: 262.301
• Mol File: 6966-15-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 461.9°C at 760 mmHg
• Flash Point: 173.5°C
• Density: 1.193g/cm³
• Vapor Pressure: 2.49E-09mmHg at 25°C
• Refractive Index: 1.551
• CAS DataBase Reference: 2-(4-methoxybenzoyl)cyclohexanecarboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-methoxybenzoyl)cyclohexanecarboxylic acid(6966-15-0)
• EPA Substance Registry System: 2-(4-methoxybenzoyl)cyclohexanecarboxylic acid(6966-15-0)

Safety Data

• Hazardous Substances Data: 6966-15-0(Hazardous Substances Data)

Usage

Structure

A cyclohexane ring with a carboxyl group (-COOH) attached to the second carbon, and a 4-methoxybenzoyl group (a benzoyl group with a methoxy substituent) attached to the same carbon.

Derivative of cyclohexanecarboxylic acid

It is a modified version of cyclohexanecarboxylic acid with the addition of a 4-methoxybenzoyl group.

Biological activity

It has potential biological activity that makes it useful in pharmaceutical research and development.

Potential applications

It may have applications in the treatment of various diseases and conditions, but further research is needed.

Building block for synthesis

Its chemical structure and properties make it a valuable building block for the synthesis of other more complex organic molecules.

Potential in drug discovery

The compound has potential in drug discovery and medicinal chemistry due to its unique structure and potential biological activity.

Upstream product

• 100-66-3 methoxybenzene 
• 13149-00-3 1,2-cis-cyclohexanedicarboxylic anhydride 
• 66107-29-7 4-methoxyphenyl triflate 
• 6966-15-0 cis-2-(4'-methoxybenzoyl)cyclohexane-1-carboxylic acid 

Downstream Products

• 736992-13-5 2-(4'-methoxybenzyl)cyclohexane-1-carboxylic acid 
• 6966-15-0 (+/-)-2t-(4-methoxy-benzoyl)-cyclohexane-r-carboxylic acid 
• 855425-02-4 2-(4'-methoxybenzyl)cyclohexane-1-carboxylic acid chloride 

Relevant articles and documents

Nickel-Catalyzed Desymmetrizing Cross-Electrophile Coupling of Cyclic Meso-Anhydrides

A Ni-catalyzed desymmetrizing cross-electrophile coupling of cyclic meso-anhydrides with aryl triflates has been successfully demonstrated. This is the only example using cyclic meso-anhydrides in cross-electrophile coupling reactions. A diverse array of valuable γ-keto acid building blocks can be generated under these conditions with excellent functional group tolerance and stereochemical fidelity.

An efficient and general method for ester hydrolysis on the surface of silica gel catalyzed by indium triiodide under microwave irradiation

Carboxylic esters are hydrolyzed to the corresponding carboxylic acids in high yields through a simple microwave assisted operation on the surface of silica gel moistened with few drops of water in presence of indium triiodide.

Cycloalkanes. Part-IV. Friedel-Crafts Condensation of cis-Cyclohexane-1,2-dicarboxylic Acid Anhydride with Aromatic Compounds and Synthesis of Simple and Substituted 2,3-Tetramethylene-5,6-benzcyclohexanes

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