54107-99-2

Basic information

• Product Name: dimethyl quinoxaline-2,3-dicarboxylate
• CAS NO: 54107-99-2
• Molecular Formula: C₁₂H₁₀N₂O₄
• Molecular Weight: 246.2188
• Mol File: 54107-99-2.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 331.2°C at 760 mmHg
• Flash Point: 154.1°C
• Density: 1.325g/cm³
• Vapor Pressure: 0.000159mmHg at 25°C
• Refractive Index: 1.603
• CAS DataBase Reference: dimethyl quinoxaline-2,3-dicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: dimethyl quinoxaline-2,3-dicarboxylate(54107-99-2)
• EPA Substance Registry System: dimethyl quinoxaline-2,3-dicarboxylate(54107-99-2)

Safety Data

• Hazardous Substances Data: 54107-99-2(Hazardous Substances Data)

Usage

General Description

Dimethyl quinoxaline-2,3-dicarboxylate is a chemical compound with the molecular formula C10H10N2O4. It is a derivative of quinoxaline and contains two methyl groups and two carboxylate groups. dimethyl quinoxaline-2,3-dicarboxylate has potential applications in the pharmaceutical and agricultural industries, as it exhibits antimicrobial and antifungal properties. Dimethyl quinoxaline-2,3-dicarboxylate may also have uses as a dye intermediate or as a building block in the synthesis of other organic compounds. Additionally, it has been studied for its potential as a corrosion inhibitor in certain industrial processes.

Upstream product

• 273-15-4 piazselenole 
• 762-42-5 dimethyl acetylenedicarboxylate 
• 4916-29-4 dimethyl 2-(phenyl-amino)-2-butendioate 
• 62-53-3 aniline 
• 146651-75-4 tert–butyl (2–aminophenyl)carbamate 
• 95-54-5 1,2-diamino-benzene 
• 221171-89-7 dimethyl 2-bromo-2H-azirine-2,3-dicarboxylate 
• 273-13-2 benzo[1,2,5]thiadiazole 
• 133-47-1 dimethyl dihydroxyfumarate 
• 67-56-1 methanol 
• 6924-99-8 Quinoxaline-2,3-dicarboxylic acid 

Downstream Products

• 6924-99-8 Quinoxaline-2,3-dicarboxylic acid 
• 5660-34-4 quinoxaline-2,3-dicarboxylic acid anhydride 
• 37648-53-6 2-(p-tolyl)-1H-pyrrolo[3,4-b]quinoxaline-1,3(2H)-dione 
• 85414-82-0 2-aminoquinoxaline-3-carboxylic acid 
• 54107-98-1 3-benzenesulfonyloxyalloxazine 
• 54108-08-6 3-hydroxy-1H-benzo[g]pteridine-2,4-dione 

Relevant articles and documents

Isobutyl Nitrite-Mediated Synthesis of Quinoxalines through Double C?H Bond Amination of N-Aryl Enamines

An efficient and metal-free double C?H bond amination of N-aryl enamines using isobutyl nitrite (IBN) has been developed. This method enables the preparation of functionalized quinoxalines in good to excellent yields and tolerates a variety of N-aryl enamines with diverse functional substituents. Mechanistic studies revealed the presence of a key β-imino oxime ester intermediate. A quinoxaline derivative could be prepared from β-carbonyl ester in one-pot sequence on a gram scale. Finally, two important quinoxaline scaffolds were easily prepared in moderate yields over two steps. (Figure presented.).

Efficient synthesis method of quinoxalinone derivatives

The invention discloses a synthesis method of quinoxalinone derivatives. According to the new route, enamine compounds obtained by synthesizing ordinary arylamine, keto ester, 3-oxo-nitrile or 1,3-dicarbonyl are used as the raw material, and 2,3-disubstit

Reactivity of 2-Halo-2H-azirines. 1. Reactions with Nucleophiles

Nucleophilic substitution reactions of 2-halo-2H-azirines 1a, 1b, 1d, and 1e with potassium phthalimide and aniline allowed the preparation of new substituted 2H-azirines 2-5. The reactions of 2-bromo-2H-azirine 1a with methylamine led to the synthesis of