7494-76-0

Usage

Uses

Used in Organic Synthesis:
4-Phenyl-cyclohexanecarboxylic acid is used as a building block for the synthesis of various organic compounds. Its carboxylic acid group allows for reactions such as esterification, amidation, and other condensation reactions, making it a versatile starting material in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
4-Phenyl-cyclohexanecarboxylic acid is used as an intermediate in the synthesis of pharmaceutical compounds. Its unique structure can be incorporated into drug molecules to impart specific biological activities, such as analgesic, anti-inflammatory, or antimicrobial properties. The development of new drugs often requires the synthesis of novel intermediates, and 4-Phenyl-cyclohexanecarboxylic acid may play a role in this process.
Used in Chemical Industry:
4-Phenyl-cyclohexanecarboxylic acid is used as a raw material in the production of specialty chemicals. Its acidic properties can be utilized in the synthesis of various chemical products, such as dyes, pigments, and polymers. 4-PHENYL-CYCLOHEXANECARBOXYLIC ACID's reactivity and structural features make it a valuable component in the development of new materials with specific properties and applications.
Used in Research and Development:
4-Phenyl-cyclohexanecarboxylic acid is used as a research compound in academic and industrial laboratories. Its unique structure and reactivity make it an interesting subject for studies in organic chemistry, materials science, and related fields. Researchers may explore its potential applications, investigate its chemical properties, or use it as a model compound for the development of new synthetic methods and techniques.

InChI:InChI=1/C13H16O2/c14-13(15)12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-5,11-12H,6-9H2,(H,14,15)

Upstream product

• 71-41-0 pentan-1-ol 
• 92-92-2 biphenyl-4-carboxylic acid 
• 32274-07-0 4-phenylcyclohexane-1-carbonitrile 
• 64-19-7 acetic acid 
• 2920-38-9 4-cyano-1,1'-biphenyl 
• 89728-29-0 2-Chlor-1-cyan-cyclohexan 
• 32379-37-6 1-Acetoxy-cyclohexylcyanid 
• 1855-63-6 cyclohex-1-enecarbonitrile 
• 636-82-8 cyclohexene-1-carboxylic acid 

Downstream Products

• 1464-90-0 4-phenyl-cyclohexanecarbonyl chloride 
• 65-85-0 benzoic acid 
• 1248776-24-0 1-hydroxy-4-phenyl-cyclohexanecarboxylic acid 
• 1596371-56-0 N-(4-(4-(2-(tert-butyl)-6-(trifluoromethyl)pyrimidin-4-yl)piperazin-1-yl)butyl)-4-phenylcyclohexanecarboxamide 
• 1159096-75-9 C₂₅H₂₉N₃O 
• 143287-94-9 1,2,3,6-tetrahydro-[1,1'-biphenyl]-4-carboxylic acid 
• 697306-44-8 N-methoxy-N-methyl-4-phenylcyclohexanecarboxamide 

Relevant academic research and scientific papers

Novel succinate derivative compounds useful as cysteine protease inhibitors

Disclosed are novel succinate derivative compounds of the formula (I)/(Ia): wherein R1, R2, R3, R4, R5, R6, R7, X and A are defined herein. The compounds are useful as inhibitors of cysteine proteases. Also disclosed are methods of using and methods of making such compounds.

Succinate derivative compounds useful as cysteine protease inhibitors

Disclosed are novel succinate derivative compounds of the formula(I)/(Ia): wherein R1, R2, R3, R4, R5, R6, R7, X and A are defined herein. The compounds are useful as inhibitors of cysteine proteases. Also disclosed are methods of using and methods of making such compounds.

Optically active pyridylethanol derivative

A novel optically active pyridylethanol derivative having a high twistability and also a superior temperature characteristic is provided, which derivative is expressed by the formula STR1 wherein R is an alkyl group of alkoxy group each of 1 to 20 carbon atoms or hydrogen atom, m and n each represent 0 or 1, STR2 each independently represent STR3 wherein Y is any one of H, halogen atom or CN and STR4 is a pyridine ring the N atom of which may be present at an optionally chosen site thereof.