75221-40-8

Usage

Uses

Used in Pharmaceutical Industry:
(4-cyclohexylmethoxy-phenyl)-acetic acid is used as a nonsteroidal anti-inflammatory drug (NSAID) for its potential analgesic and anti-inflammatory properties. It works by inhibiting the production of inflammatory molecules in the body, thereby reducing pain and inflammation.
Used in Organic Synthesis:
(4-cyclohexylmethoxy-phenyl)-acetic acid is used as a building block in the synthesis of various organic compounds due to its unique chemical structure.
Used in Medicinal Chemistry:
(4-cyclohexylmethoxy-phenyl)-acetic acid is used as a starting material in the development of new drugs and pharmaceutical agents, taking advantage of its specific structural features.

Upstream product

• 156-38-7 4-hydroxyphenylacetate 
• 5469-33-0 cyclohexylmethyl iodide 
• 14199-15-6 Methyl 4-hydroxyphenylacetate 

Downstream Products

• 89790-05-6 2-(4-Cyclohexylmethoxy-phenyl)-acetamide 

Relevant academic research and scientific papers

Synthesis and aldose reductase inhibitory activities of novel O-substituted hydroxyphenylacetic acid derivatives

In continuation of our work aimed towards the preparation of novel aldose reductase inhibitors, several O-substituted hydroxyphenylacetic acid derivatives were investigated. The highest inhibitory activity was found for compounds 7b and 7c bearing a cyclo

1- 2’ (1, 4’-BIPERIDIN-1’-YL)-1- (PHENYL) -ETHYL CYCLOHEXANOL DERIVATIVES AS MONOAMINE REUPTAKE MODULATORS FOR THE TREATMENT OF VISOMOTOR SYMPTOMS

The present invention is directed to substituted N-heterocycle derivatives of formula (I), compositions containing these derivatives, and their use in the manufacture of a medicament for the prevention and treatment of conditions ameliorated by monoamine

FUSED-ARYL AND HETEROARYL DERIVATIVES AND METHODS OF THEIR USE

The present invention is directed to fused-aryl and heteroaryl derivatives of formula I, compositions containing these derivatives, and methods of their use for the prevention and treatment of conditions ameliorated by monoamine reuptake including, inter

ARYLALKYL- AND CYCLOALKYLALKYL-PIPERAZINE DERIVATIVES AND METHODS OF THEIR USE

The present invention is directed to arylalkyl- and cycloalkylalkyl-piperazine derivatives, compositions containing these derivatives, and methods of their use for the prevention and treatment of conditions ameliorated by monoamine reuptake including, int

Design of Inhibitors from the Three-Dimensional Structure of Alcohol Dehydrogenase. Chemical Synthesis and Enzymatic Properties

Inhibitors of liver alcohol dehydrogenase were designed from the three-dimensional structure of the enzyme.The ligand to the catalytic zinc ion is an amide group or, better, a formamide group.With the latter function, a hydrogen bond between the NH group and the hydroxyl group of Ser-48 may be formed.The hydrophobic substrate binding site brings structural restraints. α-ω bifunctional molecules show good inhibitory properties possibly due to the interactions with polar residues at the entrance of the substrate binding site.