1085313-34-3

Basic information

• Product Name: (S)-methyl 2-ethoxy-3-(4-(2-(4-ethoxyphenylethylamino)-2-oxoethoxy)phenyl)propanoate
• Synonyms: (S)-methyl 2-ethoxy-3-(4-(2-(4-ethoxyphenylethylamino)-2-oxoethoxy)phenyl)propanoate
• CAS NO: 1085313-34-3
• Molecular Weight: 415.486
• Mol File: 1085313-34-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-methyl 2-ethoxy-3-(4-(2-(4-ethoxyphenylethylamino)-2-oxoethoxy)phenyl)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-methyl 2-ethoxy-3-(4-(2-(4-ethoxyphenylethylamino)-2-oxoethoxy)phenyl)propanoate(1085313-34-3)
• EPA Substance Registry System: (S)-methyl 2-ethoxy-3-(4-(2-(4-ethoxyphenylethylamino)-2-oxoethoxy)phenyl)propanoate(1085313-34-3)

Safety Data

• Hazardous Substances Data: 1085313-34-3(Hazardous Substances Data)

Upstream product

• 1085313-31-0 (S)-2-(4-(2,3-dimethoxy-3-oxopropyl)phenoxy)acetic acid 
• 56370-30-0 2-(4-ethoxyphenyl)ethanamine hydrochloride 

Relevant articles and documents

Syntheses of a selective peroxisome proliferator activated receptor modulator and practical new preparations of 2-(4-Alkoxyphenyl) ethylamines t

This article describes chemistry that was developed to give access to multigram quantities of the selective peroxisome proliferator activated receptor modulator (SPPARM), compound 1.1 Fischer esteriflcations, phase transfer-catalyzed alkylations, amide couplings, crystallizations, and a new synthesis were developed to accomplish this task. In addition, an efficient method for preparing 2-(4-alkoxyphenyl) ethylamines 7a - d from tyramine 9 was developed that involves O-alkylation of intermediate Schiff base 11 and subsequent acid-catalyzed hydrolysis to afford the target molecules as crystalline hydrochloride salts.