5181-11-3

Usage

Uses

Used in Organic Synthesis:
(2'-Methoxy-biphenyl-4-yl)-acetic acid is used as a building block in organic synthesis for the preparation of various pharmaceuticals and agrochemicals. Its unique structure allows for the creation of a wide range of compounds with different properties and applications.
Used in Chemical Production:
(2'-Methoxy-biphenyl-4-yl)-acetic acid serves as a precursor in the production of other chemical compounds, contributing to the development of new materials and products in the chemical industry.
Used in Pharmaceutical Research:
(2'-Methoxy-biphenyl-4-yl)-acetic acid is used as a subject of research for its potential biological activities, including anti-inflammatory and analgesic properties. Its exploration in pharmaceutical research aims to discover new therapeutic agents and treatments for various conditions.
Used in Agrochemical Research:
Similar to its pharmaceutical applications, (2'-Methoxy-biphenyl-4-yl)-acetic acid is also studied for its potential use in agrochemicals, where it could contribute to the development of new pesticides, herbicides, or other agricultural products to improve crop yield and protection.

Upstream product

• 5720-06-9 2-Methoxyphenylboronic acid 
• 1878-68-8 2-(4-bromophenyl)-acetic acid 

Relevant academic research and scientific papers

Fluorous-silica-supported perfluoro-tagged palladium complexes catalyze Suzuki couplings in water

Different Pd-complexes (see 2a-d and 3) with and without perfluoroalkyl tags were deposited on fluorous reversed-phase silica 1 and unmodified silica gel. These supported complexes were successfully used as precatalysts for the Suzuki reaction in H2O. H2O-Soluble aryl bromides were easily converted to the corresponding biphenyls. Although none of the complexes is H2O-soluble, the active catalyst is most likely homogeneously dissolved. Nevertheless, the Pd-leaching into the product was low.

AROMATIC AMINE DERIVATIVES, PROCESS FOR THE PREPARATION THEREOF AND AGENTS CONTAINING THE SAME

Compounds of a formula: wherein Ring A represents an optionally-substituted aromatic ring; Ring B represents an optionally-substituted cyclic hydrocarbon group; Z represents an optionally-substituted cyclic group; R1 represents a hydrogen atom, an optionally-substituted hydrocarbon group, an optionally-substituted heterocyclic group, or an acyl group; R2 represents an optionally-substituted amino group; D represents a chemical bond or a divalent group; E represents -CO-, -CON(Ra)-, COO-, -N(Ra)CON(Rb)-, -N(Ra)COO-, -N(Ra)SO2-, -N(Ra)-, -O-, -S-,-SO- or -SO2- (in which Ra and Rb each independently represent a hydrogen atom or an optionally-substituted hydrocarbon group); G represents a chemical bond or a divalent group; L represents (1) a chemical bond or (2) a divalent hydrocarbon group optionally having from 1 to 5 substituents selected from;(i) a C1-6 alkyl group,(ii) a halogeno-C1-6 alkyl group,(iii) a phenyl group,(iv) a benzyl group,(v) an optionally-substituted amino group,(vi) an optionally-substituted hydroxy group, and(vii) a carbamoyl or thiocarbamoyl group optionally substituted by: a C1-6 alkyl group, an optionally-substituted phenyl group, or an optionally-substituted heterocyclic group, and optionally interrupted by -O- or -S-; X represents an oxygen atom, an optionally-oxidized sulfur atom, an optionally-substituted nitrogen atom, or an optionally-substituted divalent hydrocarbon group; Y represents two hydrogen atoms, an oxygen atom or a sulfur atom; .... means that R2 may be bonded to the atom on Ring B to form a ring, or their salts, and a method for producing them.