3583-56-0

Upstream product

• 51-66-1 4-methoxyacetanilide 

Downstream Products

• 99942-68-4 N-(3-Chloro-phenyl)-N'-(4-methoxy-phenyl)-N-methyl-acetamidine 
• 99942-67-3 N'-(4-Methoxy-phenyl)-N-methyl-N-phenyl-acetamidine 
• 562870-93-3 N-(4-methoxyphenyl)-N-[1-(2-phenylethyl)prop-2-en-1-yl]amine 

Relevant academic research and scientific papers

Catalytic asymmetric [3,3]-rearrangements of allylic acetimidates

A streamlined synthetic access to enantiomerically pure allylic amines as advanced and valuable synthetic building blocks is important for pharmaceutical sciences. The rearrangement of allylic trihaloacetimidates is known as an attractive method to furnis

Synthesis of 3-aryl-5-methyl 4-substituted [1,2,4]triazoles

Treatment of N -substituted acetamides with oxalyl chloride generates imidoyl chlorides, which react readily with aryl hydrazides. Following cyclization, triazoles can easily be obtained in moderate to good yields. 5-Methyl triazoles can be further functionalized through α-lithiation and subsequent reaction with an electrophile. Copyright Taylor & Francis Group, LLC.