63635-28-9

Upstream product

• 63635-27-8 N-[3-(4-acetylamino-phenoxy)-2-hydroxy-propyl]-succinimide 

Downstream Products

• 63635-29-0 5-(4-amino-phenoxymethyl)-oxazolidine-2-thione 
• 63635-35-8 1-(4-methoxy-phenyl)-3-[4-(2-thioxo-oxazolidin-5-ylmethoxy)-phenyl]-thiourea 
• 63635-37-0 1-(4-bromo-phenyl)-3-[4-(2-thioxo-oxazolidin-5-ylmethoxy)-phenyl]-thiourea 
• 63635-36-9 1-(4-chloro-phenyl)-3-[4-(2-thioxo-oxazolidin-5-ylmethoxy)-phenyl]-thiourea 
• 63635-32-5 1-[4-(2-thioxo-oxazolidin-5-ylmethoxy)-phenyl]-3-m-tolyl-thiourea 
• 63635-33-6 1-[4-(2-thioxo-oxazolidin-5-ylmethoxy)-phenyl]-3-p-tolyl-thiourea 
• 63635-34-7 1-(2-methoxy-phenyl)-3-[4-(2-thioxo-oxazolidin-5-ylmethoxy)-phenyl]-thiourea 
• 63635-30-3 1-phenyl-3-[4-(2-thioxo-oxazolidin-5-ylmethoxy)-phenyl]-thiourea 
• 63635-31-4 1-[4-(2-thioxo-oxazolidin-5-ylmethoxy)-phenyl]-3-o-tolyl-thiourea 
• 63635-38-1 1-ethyl-3-[4-(2-thioxo-oxazolidin-5-ylmethoxy)-phenyl]-thiourea 

Relevant academic research and scientific papers

Synthesis of 5 substituted 2 Oxazolidinethiones and their antagonism to uterotropic effect of diethylstilbestrol

5-(4-Aminophenoxylmethyl)-2-oxazolidinethiones were synthesized by the cyclization of 1-(4-aminophenoxy)-3-amino-2-propanol in the presence of potassium hydroxide and carbon disulfide. This oxazolidinethione, on reaction with suitable isothiocyanates, yielded 5-[4-(substituted thiocarbamido)phenoxymethyl] -2-oxazolidinethiones. These compounds antagonized the uterotropic effects of diethylstilbestrol in female rats and possessed approximate LD50 values of 400->800 mg/kg.