24451-13-6

Basic information

• Product Name: (4-dimethylamino-phenyl)-oxalamic acid ethyl ester
• CAS NO: 24451-13-6
• Molecular Weight: 236.271
• Mol File: 24451-13-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (4-dimethylamino-phenyl)-oxalamic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (4-dimethylamino-phenyl)-oxalamic acid ethyl ester(24451-13-6)
• EPA Substance Registry System: (4-dimethylamino-phenyl)-oxalamic acid ethyl ester(24451-13-6)

Safety Data

• Hazardous Substances Data: 24451-13-6(Hazardous Substances Data)

Usage

Description

(4-dimethylamino-phenyl)-oxalamic acid ethyl ester is an organic compound with the molecular formula C12H16N2O3. It is an ester derived from oxalamic acid and ethyl alcohol, featuring a phenyl group with a dimethylamino substituent. (4-dimethylamino-phenyl)-oxalamic acid ethyl ester is known for its versatility and potential applications across various fields, including organic chemistry, coordination chemistry, pharmaceuticals, agrochemicals, materials science, and biochemistry.

Uses

Used in Organic Chemistry:
(4-dimethylamino-phenyl)-oxalamic acid ethyl ester serves as a reagent in various chemical reactions, contributing to the synthesis of a wide range of organic compounds.
Used as a Ligand in Coordination Chemistry:
(4-dimethylamino-phenyl)-oxalamic acid ethyl ester functions as a ligand, playing a crucial role in the formation and stabilization of metal complexes, which are essential in numerous chemical and catalytic processes.
Used in Pharmaceutical Production:
(4-dimethylamino-phenyl)-oxalamic acid ethyl ester acts as a precursor in the production of pharmaceuticals, aiding in the development of new drugs with potential therapeutic applications.
Used in Agrochemicals:
As a precursor, this compound contributes to the synthesis of agrochemicals, which are vital for enhancing crop protection and agricultural productivity.
Used in Materials Science:
(4-dimethylamino-phenyl)-oxalamic acid ethyl ester may have applications in materials science, potentially leading to the development of new materials with unique properties and uses.
Used in Biochemistry:
This versatile compound may also find uses in biochemistry, where it could be employed in the study of biological processes and the development of bioactive molecules.

Upstream product

• 99-98-9 4-amino-N,N-dimethylaniline 
• 95-92-1 oxalic acid diethyl ester 

Downstream Products

• 41116-33-0 (4-dimethylamino-phenyl)-oxalamide 
• 45869-07-6 N¹,N¹-dimethyl-benzene-1,2,4-triyltriamine 

Relevant articles and documents

Oxamic acid derivatives

Anti-allergic agents of aromatic oxamic acid derivation present the following formula: STR1 in which A is a member selected from the group consisting of α-naphthyl, β-napthtyl, phenyl, 2,6-di-chlorophenyl, and substituted phenyl moieties containing from one to three substituents in any of the 2,3,4 and 5 positions of the phenyl ring, independently selected from the group consisting of lower alkyl, lower alkylthio, lower alkylsulfinyl, lower alkoxy, hydroxy (lower)alkoxy, 2-(oxalyloxy) ethoxy, benzyloxy, N-mono- and di-lower alkylamino(lower)alkoxy, halo, sulfamyl, polyhalo(lower)alkyl, carbamyl, N-lower alkylcarbamyl, nitro, mono and di lower alkylamino, carboxy, lower alkylcarbonyl, carb(lower)alkoxy, phenoxy(lower)alkoxy, and oxalamidophenoxy radicals; and pharmaceutically acceptable salts thereof.

Oxamic acid derivatives

Anti-allergic agents of aromatic and heterocyclic oxamic acid derivation present the following formula: STR1 in which A is a member selected from the group consisting of 2-thiazolyl, 2-pyridyl, 2-pyridyl-N-oxide, 6-(lower)alkyl-2-pyridyl, 3-cyano-2-pyridyl, 3-pyridyl, 4-pyridyl, 2-pyrimidinyl, 2-pyrazinyl, α-naphthyl, β-naphthyl, phenyl, 2,6-di-chlorophenyl, and substituted phenyl moieties containing from one to three substituents in any of the 2,3,4 and 5 positions of the phenyl ring, independently selected from the group consisting of lower alkyl, lower alkylthio, lower alkylsulfinyl, lower alkoxy, hydroxy(lower)alkoxy, 2-(lower alkoxy oxalyloxy) ethoxy, benzyloxy, N-mono-and di-lower alkylamino(lower)alkoxy, halo, sulfamyl, polyhalo(lower)alkyl, carbamyl, N-lower alkylcarbamyl, nitro, mono-and di-lower alkylamino, phenylazo, carboxy, lower alkylcarbonyl, cyano, carb(lower)alkoxy, phenoxy(lower)alkoxy, lower alkoxyoxalamido and lower alkoxyoxalamidophenoxy radicals; B, when taken alone, is a member selected from the group consisting of --OH, lower alkoxy, --NH2, --NHOH, cyclohexyloxy and phenoxy; and Y is a member selected from the group consisting of oxygen and when taken with B and the carbon atom to which they are attached, forms the moiety STR2

Pyridyl oxamic acid derivatives and use in the prevention of allergic reactions

Anti-allergic agents of aromatic and heterocyclic oxamic acid derivation present the following formula: STR1 in which A is a member selected from the group consisting of 2-thiazolyl, 2-pyridyl, 2-pyridyl-N-oxide, 6-(lower)alkyl-2-pyridyl, 3-cyano-2-pyridyl, 3-pyridyl, 4-pyridyl, 2-pyrimidinyl, 2-pyrazinyl, α-naphthyl, βnaphthyl, phenyl, 2,6-dichlorophenyl, and substituted phenyl moieties containing from one to three substituents in any of the 2,3,4 and 5 positions of the phenyl ring, independently selected from the group consisting of lower alkyl, lower alkylthio, lower alkylsulfinyl, lower alkoxy, hydroxy(lower)-alkoxy, 2-(lower alkoxy oxalyloxy) ethoxy, benzyloxy, N-mono-and di-lower alkylamino(lower)-alkoxy, halo, sulfamyl, polyhalo(lower)alkyl, carbamyl, N-lower alkylcarbamyl, nitro, mono-and di-lower alkylamino, phenylazo, carboxy, lower alkylcarbonyl, cyano, carb(lower)alkoxy, phenoxy(lower)alkoxy, lower alkoxyoxalamido and lower alkoxyoxalamidophenoxy radicals; B, when taken alone, is a member selected from the group consisting of --OH, lower alkoxy, --NH2, --NHOH, cyclohexyloxy and phenoxy; and Y is a member selected from the group consisting of oxygen and when taken with B and the carbon atom to which they are attached, forms the moiety STR2