13120-33-7

Usage

Uses

Used in Pharmaceutical Industry:
[methyl(phenyl)amino](oxo)acetic acid is used as a building block for the synthesis of various drugs and pharmaceuticals. Its unique structure allows it to be a key component in the development of new medications, contributing to the advancement of healthcare and treatment options.
Used in Organic Chemistry:
[methyl(phenyl)amino](oxo)acetic acid may have potential applications in the field of organic chemistry, where it can be utilized in various chemical reactions and processes. Its unique structure and properties make it a valuable compound for research and development in this field.
Used in Material Science:
[methyl(phenyl)amino](oxo)acetic acid may also find applications in material science, where it can be used to develop new materials with specific properties. Its unique structure and properties can contribute to the creation of innovative materials with potential uses in various industries.

InChI:InChI=1/C9H9NO3/c1-10(8(11)9(12)13)7-5-3-2-4-6-7/h2-6H,1H3,(H,12,13)

Upstream product

• 39581-30-1 3-(N-methyl-N-phenylamino)-3-oxopropanenitrile 
• 51680-04-7 2-chloro-N-methyl-2-oxo-N-phenylacetamide 
• 124-38-9 carbon dioxide 
• 4860-71-3 4-methyl-3-oxo-1-oxy-3,4-dihydro-quinoxaline-2-carboxylic acid N-methyl-anilide 
• 100-61-8 N-methylaniline 
• 137409-99-5 methyl 2-(methyl(phenyl)amino)-2-oxoacetate 

Downstream Products

• 1343395-48-1 3-(4-chlorophenyl)-N-methyl-N-phenylprop-2-ynamide 
• 94298-51-8 N-methyl-N,3-diphenylprop-2-ynamide 
• 1013905-87-7 N-methyl-N-phenyl-3-(4-methylphenyl)propargylamide 
• 93-61-8 N-methyl-N-phenylformamide 
• 67752-52-7 ethyl 2-oxo-1,2,3,4-tetrahydroquinoline-4-carboxylate 
• 18859-05-7 4-cyano-N-methyl-N-phenylbenzamide 

Relevant academic research and scientific papers

Carbamoyl Radicals via Photoredox Decarboxylation of Oxamic Acids in Aqueous Media: Access to 3,4-Dihydroquinolin-2(1 H)-ones

The first visible-light-mediated photoredox oxidative approach for generating carbamoyl radicals from oxamic acids is disclosed. Reaction of the generated carbamoyl radicals with electron-deficient alkenes opens efficient access to 3,4-dihydroquinolin-2(1H)-ones under mild conditions through a sequence of intermolecular radical addition, cyclization, and aromatization. The process is compatible with a variety of oxamic acids and electron-deficient alkenes, and a wide variety of 3,4-dihydroquinolin-2(1H)-ones were prepared.

Synthetic method of quinolinone compounds

The invention discloses a synthetic method of quinolinone compounds. The synthetic method is characterized by comprising the following steps: taking aniline and oxalyl chloride as raw materials, carrying out stirring in an organic solvent, sequentially ad

N,N-DISUBSTITUTED LITHIUM BIS(CARBAMOYL)CUPRATE. A CONVENIENT COMPLEX FOR ONE-POT CONVERSIONS OF AMINES TO FORMAMIDES, OXAMIDES, CARBAMATES, AND OXAMIC ACIDS

Lithium bis(carbamoyl)cuprates (2) were readily derived from secondary amines such as N-methylaniline, N-methylbenzylamine, and diethylamine, under mild carbonylation conditions (0 deg C, 1 atm of carbon monoxide), but diphenylamine and benzylphenylamine were unsuitable as the starting materials.The carbamoylcopper complexes 2 formed in ether were readily converted to the corresponding formamides, oxamides, carbamates, and oxamic acids by the appropriate treatment.The formation and stability of 2 depended much on the solvent used.The higher polarity effect of the solvent (DME, THF, and HMPA) made 2 less stable and caused concomitant evolution of carbon monoxide in further reactions.A palladium catalyst was found to be effective for cross-coupling reactions of 2 with iodobenzene or (E)-β-bromostyrene.