518343-99-2

Basic information

• Product Name: 2-benzylamino-4-[4-(1-ethoxycarbonyl-1-methyl-ethoxy)-phenoxy]-butyric acid ethyl ester
• Synonyms: 2-benzylamino-4-[4-(1-ethoxycarbonyl-1-methyl-ethoxy)-phenoxy]-butyric acid ethyl ester
• CAS NO: 518343-99-2
• Molecular Weight: 443.54
• Mol File: 518343-99-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-benzylamino-4-[4-(1-ethoxycarbonyl-1-methyl-ethoxy)-phenoxy]-butyric acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-benzylamino-4-[4-(1-ethoxycarbonyl-1-methyl-ethoxy)-phenoxy]-butyric acid ethyl ester(518343-99-2)
• EPA Substance Registry System: 2-benzylamino-4-[4-(1-ethoxycarbonyl-1-methyl-ethoxy)-phenoxy]-butyric acid ethyl ester(518343-99-2)

Safety Data

• Hazardous Substances Data: 518343-99-2(Hazardous Substances Data)

Upstream product

• 518344-00-8 2-amino-4-[4-(1-ethoxycarbonyl-1-methyl-ethoxy)-phenoxy]-butyric acid ethyl ester 
• 518343-91-4 2-acetylamino-2-{2-[4-(1-ethoxycarbonyl-1-methyl-ethoxy)phenoxy]-ethyl}-malonic acid diethyl ester 
• 518343-90-3 2-[4-(2-bromoethoxy)-phenoxy]-2-methyl-propionic acid ethyl ester 
• 42806-90-6 2-(4-hydroxyphenoxy)-2-methyl propionic acid ethyl ester 

Downstream Products

• 518344-02-0 2-[benzyl-(biphenyl-4-carbonyl)-amino]-4-[4-(1-carboxy-1-methyl-ethoxy)-phenoxy]-butyric acid 
• 328918-72-5 2-{4-[2-(2-biphenyl-4-yl-5-trifluoromethyl-oxazol-4-yl)-ethoxy]-phenoxy}-2-methyl-propionic acid 
• 328920-00-9 2-{4-[2-(2-biphenyl-4-yl-5-trifluoromethyl-oxazol-4-yl)-ethoxy]-phenoxy}-2-methyl-propionic acid methyl ester 
• 518344-01-9 2-[benzyl-(biphenyl-4-carbonyl)-amino]-4-[4-(1-ethoxycarbonyl-1-methyl-ethoxy)-phenoxy]-butyric acid ethyl ester 

Relevant articles and documents

Application of the Dakin-West reaction for the synthesis of oxazole-containing dual PPARα/γ agonists

An improved method for the preparation of a series of oxazole-containing dual PPARα/γ agonists is described. A synthetic sequence utilizing a Dakin-West reaction was devised that allows for the introduction of the oxazole ring either late in the synthetic sequence via aminomalonate-derived chemistry or in pivotal SAR intermediates derived from aspartic acid.