15267-81-9

Upstream product

• 64-17-5 ethanol 
• 5327-91-3 (4-ethoxyphenoxy)acetic acid 
• 622-62-8 4-Ethoxyphenol 
• 105-36-2 ethyl bromoacetate 

Downstream Products

• 14771-58-5 N,N-Diethyl-N'-<(4-ethoxy-phenoxy)-acetyl>-ethylendiamin 
• 15267-82-0 <4-Aethoxy-phenoxy>-acethydroxamsaeure 

Relevant academic research and scientific papers

A pillar[5]arene with an amino-terminated arm stabilizes the formation of aliphatic hemiaminals and imines

We report a new mono-armed pillar[5]arene with the amino-substituent self-included in the pillarene cavity, which can stabilize the hemiaminals and imines formed from the reaction of aliphatic amines and aldehydes as monitored by mass spectroscopy.

16-Phenoxy and 16-substituted phenoxy-prostatrienoic acid derivatives

Novel racemic and 8R-antimeric 16-phenoxy- and 16-(o, m or p)-substituted phenoxy derivatives of 9α, 11α,15-trihydroxy-17,18,19,20-tetranorprosta-4,5,13-trans-trienoic acids, which may be further substituted at C-15 by a methyl or ethyl group, the pharmaceutically acceptable, non-toxic lower alkyl esters and salts thereof and processes for the production of such compounds. dl 9α,11α,15α-trihydroxy-16-m-trifluoromethylphenoxy-17,18,19,20-tetranorprosta-4,5,13-trans-trienoic acid and dl 9α,11α,15 -trihydroxy-15 -methyl-16-m-trifluoromethylphenoxy-17,18,19,20-tetranorprosta-4,5,13-trans-trienoic acid are representative compounds of the class. These compounds possess prostaglandin-like activities and thus are useful in the treatment of mammals where prostaglandins are indicated. They are particularly useful as luteolytic agents in female mammals.