20916-14-7

Upstream product

• 20142-88-5 2-(4-nitrophenoxy)acetyl chloride 
• 74-89-5 methylamine 
• 19076-89-2 ethyl 4-nitrophenoxyacetate 
• 52547-48-5 (4-amino-phenoxy)-acetic acid methylamide 
• 1798-11-4 4-nitrophenoxyacetic acid 
• 143666-76-6 N-benzyl-N-methyl-(4-nitrophenoxy)acetylamide 
• 94-75-7 2,4-Dichlorophenoxyacetic acid 
• 593-51-1 methylamine hydrochloride 

Downstream Products

• 52547-48-5 (4-amino-phenoxy)-acetic acid methylamide 
• 110506-70-2 2-(4-Isothiocyanato-phenoxy)-N-methyl-acetamide 

Relevant academic research and scientific papers

Room-temperature debenzylation of N-benzylcarboxamides by N-bromosuccinimide

A simple and highly efficient method has been developed with which to cleave the N-benzyl group on N-mono- or disubstituted carboxamides using N-bromosuccinimide (NBS) at room temperature. All the 31 substrates examined showed moderate to excellent deprotection yields. Our study also indicated that the debenzylation may involve an oxygen/light initiated free radical mechanism. Georg Thieme Verlag Stuttgart.

Synthesis of nitrogen-containing phenoxyacetic acid derivatives

Nitrogen-containing phenoxyacetic acid derivatives were synthesized by reactions of substituted phenoxyacetic acids with amines, urea, and ethyl carbamate.

Synthesis of Some New 3-Methoxy-4-acylaminophenylisothiocyanates, 4'-Isothiocyanatophenoxyacetamides/Isobutyramides as Possible Anthelmintic Agents

A number of new 3-methoxy-4-acylaminophenylisothiocyanates (II and III), 4'-isothiocyanatophenoxyacetamides (IV) and 4-isothiocyanatophenoxyisobutyramides (V) have been synthesized and tested for anthelmintic, antiamoebic and antitrichomonal activities.