26583-49-3

Usage

Type of compound

Acyl chloride

Derivation

Derived from 3-methylphenoxypropanoic acid

Molecule structure

A 3-methylphenoxy group attached to a propanoyl chloride group

Usage

+ Synthesis of various pharmaceuticals and agrochemicals
+ Production of non-steroidal anti-inflammatory drugs (NSAIDs)
+ Starting material for the synthesis of other organic compounds
+ Reagent in organic synthesis
+ Building block for the creation of new molecules with potential pharmacological activity.

Upstream product

• 25140-95-8 2-(3-methylphenoxy)propionic acid 
• 108-39-4 3-methyl-phenol 
• 3019-89-4 sodium 3-methylphenoxide 
• 125095-33-2 Methyl 2-(3-methylphenoxy)propionate 
• 152855-53-3 Ethyl 2-(3-methylphenoxy)propionate 
• 36294-16-3 potassium m-methylphenoxide 

Downstream Products

• 54365-78-5 2,6-Dimethylbenzofuran-3(2H)-one 
• 924257-06-7 N-(2-morpholinyl-5-trifluoromethylphenyl)-2-(3-methylphenoxy)propanamide 
• 93304-72-4 Marmelerin 
• 7137-22-6 2,3,6-trimethylbenzofuran 
• 1048953-51-0 N-(2-fluoro-5-(3-methyl-2,6-dioxo-4-(trifluoromethyl)-2,3-dihydro-pyrimidin-1(6H)-yl)phenyl)-2-(m-tolyloxy)propanamide 

Relevant academic research and scientific papers

Copper-catalyzed: Ortho -C(sp2)-H amination of benzamides and picolinamides with alkylamines using oxygen as a green oxidant

A versatile Cu-catalyzed direct ortho-C(sp2)-H amination of benzamides and picolinamides with alkylamines has been achieved. This method employs cheap and eco-friendly copper as a catalyst and oxygen as an oxidant, and also has the advantages of straightf

A N - (2 - morpholinyl -5 - trifluoromethyl phenyl) -2 - (3 - methylphenoxy) propionamide preparation method (by machine translation)

The invention discloses a N - (2 - morpholinyl - 5 - trifluoromethyl-phenyl) - 2 - (3 - methylphenoxy) propionamide of the preparation method, comprises the following steps: The invention provides N - (2 - morpholinyl - 5 - trifluoromethyl-phenyl) - 2 -

Synthesis of N- 2-pyrrolidinone as antimicrobial agent

Several N- 2-pyrrolidinones have been synthesised and screened for their antibacterial and antifungal activities. their structures have been elucidated on the basis of elemental analysis and spectral data.

Antiphlogistic aryloxypropionic acids: Configurational study

Configurational relationships of a series of antiphlogistic 2-aryloxypropionyl derivatives by means of 1H-NMR and HPLC methods were demonstrated. NMR spectra of racemic mixtures and optically active esters were recorded by adding suitable quant