1600521-44-5

Usage

Uses

Used in Organic Synthesis:
N-(3-(diphenylphosphoryl)phenyl)acetamide is used as an intermediate in organic synthesis for the preparation of various complex organic molecules. Its unique structure and reactivity allow for the formation of new chemical bonds and the synthesis of a wide range of compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, N-(3-(diphenylphosphoryl)phenyl)acetamide is used as a starting material or intermediate in the development of new drugs. Its potential as a precursor for the synthesis of bioactive molecules makes it a valuable tool in medicinal chemistry.
Used in Material Science:
N-(3-(diphenylphosphoryl)phenyl)acetamide may also have applications in the development of new materials, such as polymers, coatings, or composites, due to its unique chemical properties and the ability to form stable bonds with other molecules.
Used in Phosphoryl Group Chemistry:
The study of phosphoryl group chemistry is an important area of research, and N-(3-(diphenylphosphoryl)phenyl)acetamide serves as a model compound for understanding the reactivity and properties of phosphoryl groups. This knowledge can be applied to the development of new catalysts, sensors, or other functional materials.

Upstream product

• 78887-39-5 3-Acetamidophenylboronic acid 
• 4559-70-0 Diphenylphosphine oxide 
• 19230-45-6 N-(3-iodophenyl)acetamide 

Relevant academic research and scientific papers

Room Temperature C-P Bond Formation Enabled by Merging Nickel Catalysis and Visible-Light-Induced Photoredox Catalysis

A novel and efficient C-P bond formation reaction of diarylphosphine oxides with aryl iodides was achieved by combining nickel catalysis and visible-light-induced photoredox catalysis. This dual-catalytic reaction showed a broad substrate scope, excellent functional group tolerance, and afforded the corresponding products in good to excellent yields. Compared with the previously reported use of photoredox/nickel dual catalysis in the construction of C-C bonds, the methodology described herein was observed to be the first to allow for C-heteroatom bond formation.

Palladium-catalyzed air-based oxidative coupling of arylboronic acids with H-phosphine oxides leading to aryl phosphine oxides

We present a novel and highly efficient methodology that allows for the construction of C-P bonds via the palladium-catalyzed air-based oxidative coupling of various commercially available arylboronic acids with easily oxidized H-phosphine oxides leading to valuable aryl phosphine oxides, particularly triarylphosphine oxides, with the use of air as the green oxidant, broad substrate applicability and good to excellent yields. The described catalytic system should be an efficient complement to the Chan-Lam type reaction and be useful in synthetic programs. This journal is the Partner Organisations 2014.