537-80-4

Usage

Uses

Used in Pharmaceutical Industry:
2,2,2-Trifluoroethyl-N-4-methoxyphenylcarbamate is used as an intermediate in the synthesis of various drugs and agrochemicals. Its carbamate functionality allows it to be a key component in the development of new pharmaceutical compounds.
Used in Agrochemical Industry:
In the agrochemical industry, 2,2,2-trifluoroethyl-N-4-methoxyphenylcarbamate has the potential to act as a pesticide, fungicide, or herbicide. Its carbamate group provides it with the necessary properties to be effective in controlling pests and diseases in agriculture.
Used in Medicinal Chemistry:
2,2,2-Trifluoroethyl-N-4-methoxyphenylcarbamate may also have applications in the field of medicinal chemistry due to its potential biological activity. Its unique structure and properties could contribute to the discovery of new therapeutic agents and treatments.
However, it is important to note that further research is needed to fully understand the potential uses and properties of 2,2,2-trifluoroethyl-N-4-methoxyphenylcarbamate. As our understanding of this chemical compound grows, so too will its potential applications in various industries.

Upstream product

• 75-89-8 2,2,2-trifluoroethanol 
• 5416-93-3 4-Methoxyphenyl isocyanate 
• 100-66-3 methoxybenzene 
• 27746-99-2 2,2,2-trifluoroethyl chloroformate 
• 104-94-9 4-methoxy-aniline 
• 1513-87-7 bis(2,2,2-trifluoroethyl) carbonate 
• 3424-93-9 4-methoxyphenylacetamide 

Downstream Products

• 62774-59-8 N-(4-methoxyphenyl)hydrazinecarboxamide 

Relevant academic research and scientific papers

Electrochemically induced Hofmann rearrangement

Electrochemically induced Hofmann rearrangement under new solvent systems containing a variety of alcohols was developed. Since the reaction proceeds under mild conditions (neutral), a variety of carbamates possessing various alkoxy moieties could be easi

Intermolecular chemo- and regioselective aromatic C-H amination of alkoxyarenes promoted by rhodium nitrenoids

Intermolecular aromatic C(sp2)-H amination promoted by neutral rhodium nitrenoids has been developed. The reactions proceeded with various oxygen-substituted arenes (1.5 equiv.) in a chemo- and regioselective manner. The aromatic C(sp2)-H amination took place at the para position of the oxygen substituent in the presence of benzylic C(sp3)-H bonds and/or C(sp3)-H bonds α to ethereal oxygen.

Facile one-pot synthesis of 4-substituted semicarbazides

A diverse library of twenty-five 4-mono- and disubstituted semicarbazides was prepared in a one-pot two-step approach. The method includes formation of a carbamate from bis(2,2,2-trifluoroethyl)carbonate or 2,2,2-trifluoroethylchloroformate and a primary or secondary amine and subsequent interaction of the carbamate with hydrazine to result in a semicarbazide. The approach allowed to obtain 4-substituted semicarbazides on a large scale in good yield and high purity. This journal is