4513-73-9

Usage

Uses

Used in Pharmaceutical Synthesis:
4-Methoxy-3-methylphenylacetic acid is used as a precursor in the synthesis of various pharmaceuticals, contributing to the development of new drugs and biologically active compounds. Its unique structure allows it to be a key component in creating molecules with specific therapeutic properties.
Used in Organic Compound Production:
This chemical is also utilized as a building block in the production of a range of organic compounds, highlighting its versatility in organic chemistry and its ability to form the basis of complex molecular structures.
Used in Material and Chemical Development:
4-Methoxy-3-methylphenylacetic acid may have applications in the development of new materials and chemicals, indicating its potential use in various industries beyond pharmaceuticals, such as in the creation of novel polymers or other advanced materials with specific properties.

InChI:InChI=1/C10H12O3/c1-7-5-8(6-10(11)12)3-4-9(7)13-2/h3-5H,6H2,1-2H3,(H,11,12)

Upstream product

• 7664-93-9 sulfuric acid 
• 859979-73-0 ethyl 2-(4-methoxy-3-methylphenyl)-2-oxoacetate 
• 10035-10-6 hydrogen bromide 
• 64-19-7 acetic acid 
• 578-58-5 2-methylmethoxybenzene 
• 60736-71-2 3-methyl-4-methoxybenzyl chloride 
• 95-48-7 ortho-cresol 
• 32723-67-4 3-methyl-4-anisaldehyde 
• 59931-48-5 4-methoxy-3-methylbenzoyl chloride 
• 6880-04-2 4-methoxy-3-methylbenzoic acid 
• 83823-58-9 1-methylsulfinyl-1-methylthio-2-(4-methoxy-3-methylphenyl)ethylene 
• 29121-56-0 (4-hydroxy-3-methylphenyl)acetic acid 
• 77-78-1 dimethyl sulfate 
• 75391-57-0 2-(4-methoxy-3-methylphenyl)acetonitrile 

Downstream Products

• 4513-72-8 4-methoxy-3-methylphenylacetyl chloride 
• 149555-53-3 N-octyl-4-methoxy-3-methylphenylacetamide 
• 1015484-08-8 C₂₄H₂₅N₅O₃ 
• 87776-77-0 2-(4-methoxy-3-methylphenyl)ethanol 
• 29076-19-5 methyl 2-(4-methoxy-3-methylphenyl)acetate 
• 950502-89-3 [3-({tert-butoxycarbonyl-[2-(2-fluoro-phenyl)-ethyl]-amino}-methyl)-4-methoxy-phenyl]-acetic acid methyl ester 
• 950502-90-6 [2-(2-fluoro-phenyl)-ethyl]-[5-(2-hydroxy-ethyl)-2-methoxy-benzyl]-carbamic acid tert-butyl ester 
• 950502-88-2 (3-{[2-(2-fluoro-phenyl)-ethylamino]-methyl}-4-methoxy-phenyl)-acetic acid methyl ester 
• 950502-87-1 (3-formyl-4-methoxy-phenyl)-acetic acid 
• 1335093-73-6 N-(2-(3-(2-fluoroethoxy)-4-methoxyphenyl)-2-methoxyethyl)-2-(4-methoxy-3-methylphenyl)acetamide 
• 1335093-76-9 N-(2-(4-(2-fluoroethoxy)-3-methoxyphenyl)-2-methoxyethyl)-2-(4-methoxy-3-methylphenyl)acetamide 
• 950502-86-0 2-(3-(bromomethyl)-4-methoxyphenyl)acetic acid 
• 1467707-70-5 3-bromo-5-methyl-4-methoxyphenylacetic acid 
• 29121-56-0 (4-hydroxy-3-methylphenyl)acetic acid 

Relevant academic research and scientific papers

Quinolones as gonadotropin releasing hormone (GnRH) antagonists: Simultaneous optimization of the C(3)-aryl and C(6)-substituents

A series of 3-arylquinolones was prepared and evaluated for their ability to act as gonadotropin releasing hormone (GnRH) antagonists. A variety of substitution patterns of the 3-aryl substituent are described. The 3,4,5-trimethylphenyl substituent (23h) was found to be optimal. (C) 2000 Elsevier Science Ltd. All rights reserved.