70044-37-0

Upstream product

• 51264-73-4 Ethyl-2-(4-formylphenoxy)propionat 
• 123-08-0 4-hydroxy-benzaldehyde 

Downstream Products

• 68113-37-1 Ethyl-2-<4-(chlormethyl)-phenoxy>-propionat 
• 66287-30-7 2-<4-(4-Chlorphenoxymethyl)phenoxy>-propanol 
• 68113-14-4 2-(4-p-Tolyloxymethyl-phenoxy)-propionic acid ethyl ester 
• 68113-12-2 2-[4-(4-Bromo-phenoxymethyl)-phenoxy]-propionic acid ethyl ester 
• 68113-31-5 Cyclopropanecarboxylic acid 2-[4-(4-chloro-phenoxymethyl)-phenoxy]-propyl ester 
• 68113-09-7 Propionsaeure-2-<4-(4-chlorphenoxymethyl)phenoxy>-propylester 
• 68113-11-1 2-[4-(2,4-Dichloro-phenoxymethyl)-phenoxy]-propionic acid ethyl ester 
• 68113-17-7 2-[4-(4-Chloro-phenoxymethyl)-phenoxy]-propionic acid hexyl ester 
• 68113-07-5 Ethyl-2-<(4-chlorphenoxymethyl)phenoxy>-propionat 
• 68113-15-5 Butyl-2-<4-(4-chlorphenoxymethyl)-phenoxy>-propionat 
• 905557-98-4 2-[4-(12-β-artemisinoxymethyl)phenoxy]propionic acid 
• 905557-97-3 2-[4-(12-α-artemisinoxymethyl)phenoxy]propionic acid 

Relevant academic research and scientific papers

Synthesis and immunosuppressive activity of new artemisinin derivatives. Part 2: 2-[12(β or α)-Dihydroartemisinoxymethyl(or 1′-ethyl)]phenoxyl propionic acids and esters

Another series of novel dihydroartemisinin derivatives were synthesized and assessed for their cytotoxicity of lymphocyte, inhibitory activity on mitogen-induced spleen lymphocyte proliferation in vitro. Some of the compounds exhibited inhibitory effects on ConA-induced T cell and LPS-induced B cell proliferation comparable to or more potent than parent artemisinin.

Synthesis and Herbicidal Effect of Substituted Phenoxymethylphenoxypropionic Acid Derivatives

Compounds are herbicides with high activity.Methods for synthesis are reported. - Keywords: Phenoxymethylphenoxypropionates, Biological Activity