853302-27-9

Basic information

• Product Name: S-2-ethoxy-3-[4-(R-1-carboxyethoxy)phenyl]propionic acid isopropyl ester
• Synonyms: S-2-ethoxy-3-[4-(R-1-carboxyethoxy)phenyl]propionic acid isopropyl ester
• CAS NO: 853302-27-9
• Molecular Weight: 324.374
• Mol File: 853302-27-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: S-2-ethoxy-3-[4-(R-1-carboxyethoxy)phenyl]propionic acid isopropyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: S-2-ethoxy-3-[4-(R-1-carboxyethoxy)phenyl]propionic acid isopropyl ester(853302-27-9)
• EPA Substance Registry System: S-2-ethoxy-3-[4-(R-1-carboxyethoxy)phenyl]propionic acid isopropyl ester(853302-27-9)

Safety Data

• Hazardous Substances Data: 853302-27-9(Hazardous Substances Data)

Upstream product

• 251454-49-6 (2S)-3-[4-(benzyloxy)phenyl]-2-ethoxypropanoic acid 
• 405271-21-8 2-ethoxy-3-(4-benzyloxyphenyl)propionic acid isopropyl ester 
• 29617-66-1 (S)-2-chloropropanoic acid 
• 325793-71-3 (S)-2-ethoxy-3-(4-hydroxyphenyl)propanoic acid isopropyl ester 

Downstream Products

• 856258-53-2 S-2-ethoxy-3-(4-{R-1-[2-(4-ethylphenyl)ethylcarbamoyl]ethoxy}phenyl)propionic acid isopropyl ester 

Relevant articles and documents

Synthesis of PPAR agonist via asymmetric hydrogenation of a cinnamic acid derivative and stereospecific displacement of (S)-2-chloropropionic acid

(Chemical Equation Presented) The synthesis of the peroxime proliferator activated receptor (PPAR) α,γ-agonist (1) was accomplished with high enantio- and diastereoselectivity by employing an asymmetric hydrogenation strategy, of an α-alkoxy cinnamic acid