128760-23-6

Basic information

• Product Name: Propanoic acid, 2-(2-methylphenoxy)-, ethyl ester
• CAS NO: 128760-23-6
• Molecular Formula: C12H16O3
• Molecular Weight: 208.257
• Mol File: 128760-23-6.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Propanoic acid, 2-(2-methylphenoxy)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Propanoic acid, 2-(2-methylphenoxy)-, ethyl ester(128760-23-6)
• EPA Substance Registry System: Propanoic acid, 2-(2-methylphenoxy)-, ethyl ester(128760-23-6)

Safety Data

• Hazardous Substances Data: 128760-23-6(Hazardous Substances Data)

Upstream product

• 535-11-5 Ethyl 2-bromopropionate 
• 4549-72-8 sodium o-cresolate 
• 95-48-7 ortho-cresol 
• 584-08-7 potassium carbonate 
• 90-02-8 salicylaldehyde 
• 3235-09-4 potassium o-cresolate 
• 29040-33-3 ethyl 2-(o-formylphenoxy)propionate 

Downstream Products

• 401791-38-6 3-(4-Benzyloxy-phenyl)-3-hydroxy-2-methyl-2-o-tolyloxy-propionic Acid Ethyl Ester 
• 86098-42-2 2-o-Tolyloxy-propionic acid hydrazide 
• 74225-90-4 ethyl 2-[2-(bromomethyl)phenoxy]propionate 
• 63986-71-0 2-o-Tolyloxy-propionyl chloride 
• 156462-59-8 2-methyl-3-(2-methylphenyl)oxy-1-butene 
• 156462-55-4 1,1-dimethyl-2-(2-methylphenyl)oxypropanol 
• 7345-21-3 2-(o-tolyloxy)propanoic acid 

Relevant articles and documents

INHIBITORS TO TARGET HIV-1 NEF-CD80/CD86 INTERACTIONS FOR THERAPEUTIC INTERVENTION

The compounds of Formula I, II, and III along with their stereoisomers, pharmaceutically acceptable salts, polymorphs, solvates and hydrates thereof are described in the present disclosure. The said compounds restore immune activation in case of infections or a disease associated with an HIV infection in a subject in need thereof.

Facile syntheses of 2-alkyl-2,3-dihydro-2-methylbenzofuran derivatives

Various 2-alkyl-2,3-dihydro-2-methylbenzofurans 4 can be easily synthesized from 2-aryloxypropionic acid ethyl esters 1 by 3 steps in good yields.

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