62351-80-8

Basic information

• Product Name: 1,2-Benzenedicarboxylic acid, 3-aMino-, 1,2-diethyl ester
• Synonyms: 1,2-Benzenedicarboxylic acid, 3-aMino-, 1,2-diethyl ester;diethyl 3-aminophthalate
• CAS NO: 62351-80-8
• Molecular Formula: C₁₂H₁₅NO₄
• Molecular Weight: 237.2518
• Mol File: 62351-80-8.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2-Benzenedicarboxylic acid, 3-aMino-, 1,2-diethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Benzenedicarboxylic acid, 3-aMino-, 1,2-diethyl ester(62351-80-8)
• EPA Substance Registry System: 1,2-Benzenedicarboxylic acid, 3-aMino-, 1,2-diethyl ester(62351-80-8)

Safety Data

• Hazardous Substances Data: 62351-80-8(Hazardous Substances Data)

Usage

Common Uses

Manufacturing of polymers and plastics

Derivation

Reaction of 1,2-benzenedicarboxylic acid and ethylamine

Structural Features

Two ethyl ester groups
An amino functional group attached to the benzene ring

Properties

High heat stability
Resistance to chemicals

Applications

Industrial products
Synthesis of pharmaceutical intermediates
Synthesis of agrochemicals

Reactivity

Versatile due to functional groups

Safety Precautions

Handle and store with care due to potential health and environmental hazards

Upstream product

• 62351-79-5 3-nitrobenzene-1,2-dicarboxylate ester 
• 623-91-6 diethyl Fumarate 
• 603-11-2 3-nitrophthalic acid 
• 88-99-3 benzene-1,2-dicarboxylic acid 
• 67-56-1 methanol 
• 75-03-6 ethyl iodide 

Downstream Products

• 24736-82-1 diethyl 3-hydroxyphthalate 
• 67193-50-4 3-iodo-phthalic acid diethyl ester 
• 28418-88-4 3-iodophthalic anhydride 
• 601-97-8 3-hydroxyphthalic acid 
• 6937-34-4 3-iodophthalic acid 
• 127413-58-5 diethyl 3-bromophthalate 
• 1005516-26-6 3-(butylamino)phthalic acid 
• 1234360-84-9 C₁₆H₂₃NO₄ 

Relevant articles and documents

Molecular properties of 5-(1H-Benzo[D]Oxa, thia, imid azole-2-Yl)-2-methyl quinazolin-4-ol fluorescent brighteners: Theoretical and experimental approach

A series of seven new fluorescent brighteners 5-(1H-benzo[d]oxazole, thiazole, imidazole-2-yl)-2-methyl quinazolin-4-ol were synthesized by chemical reaction of 2-Methyl-4-oxo-3,4-dihydroquinazoline-5-carboxylic acid and derivatives of 2-aminophenol/2-ami

2-methyl-4-oxo-N-(4-oxo-2-phenyl substituted-1,3-thiazolidin-3-yl)-3,4- dihydroquinazoline-5-carboxamides - A new range of fluorescent whiteners: Synthesis and photophysical characterization

Fluorescent quinazolinones were synthesized form ethyl 2-methyl-4-oxo-3,4- dihydroquinazoline -5-carboxylate intermediate. The photophysical properties of the compounds were evaluated in DMF solvent. The experimental absorption and emission of the compoun

Metallo-β-lactamase inhibitory activity of 3-alkyloxy and 3-amino phthalic acid derivatives and their combination effect with carbapenem

3-Alkyloxy and 3-amino phthalic acid derivatives were found to have metallo-β-lactamase inhibitory activity. Among them, 3-amino phthalic acid derivatives showed both potent activity against metallo-β-lactamase, IMP-1 inhibitory activity and a strong combination effect with biapenem (BIPM), carbapenem antibiotic. In particular, the 4′-hydroxy-piperidine derivative showed strong IMP-1 inhibitory activity and a combination effect with various antibiotics.