27693-67-0

Basic information

• Product Name: 2,3'-IMINO-DIBENZOIC ACID
• Synonyms: 2,3'-IMINO-DIBENZOIC ACID;N-(3-carboxyphenyl)anthranilic acid;2-((3-Carboxyphenyl)aMino)benzoic acid
• CAS NO: 27693-67-0
• Molecular Formula: C₁₄H₁₁NO₄
• Molecular Weight: 257.24144
• Mol File: 27693-67-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 492.7°Cat760mmHg
• Flash Point: 251.8°C
• Appearance: /
• Density: 1.424g/cm³
• Vapor Pressure: 1.59E-10mmHg at 25°C
• Refractive Index: 1.696
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2,3'-IMINO-DIBENZOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3'-IMINO-DIBENZOIC ACID(27693-67-0)
• EPA Substance Registry System: 2,3'-IMINO-DIBENZOIC ACID(27693-67-0)

Safety Data

• Hazardous Substances Data: 27693-67-0(Hazardous Substances Data)

Usage

General Description

2,3'-Imino-dibenzoic acid is a chemical compound with the molecular formula C13H9NO2, and it is commonly used as a fluorescent probe in biochemical and molecular biology research. It is also known as DB 1, and it has a yellow-green fluorescence when bound to DNA, which makes it useful for detecting and visualizing nucleic acids in biological samples. 2,3'-IMINO-DIBENZOIC ACID has been used to study the binding interactions between DNA and various ligands, as well as to investigate the structural and conformational changes in nucleic acids. Additionally, 2,3'-imino-dibenzoic acid has been used as a ligand in coordination chemistry and catalysis, demonstrating its versatility and potential applications in various scientific fields.

InChI:InChI=1/C14H11NO4/c16-13(17)9-4-3-5-10(8-9)15-12-7-2-1-6-11(12)14(18)19/h1-8,15H,(H,16,17)(H,18,19)

Upstream product

• 16463-38-0 potassium 2-chlorobenzoate 
• 99-05-8 meta-aminobenzoic acid 
• 118-91-2 ortho-chlorobenzoic acid 
• 114918-37-5 methyl 2-<(3-carbomethoxyphenyl)amino>benzoate 
• 618-89-3 methyl 3-bromobenzoate 
• 134-20-3 2-carbomethoxyaniline 
• 4518-10-9 Methyl 3-aminobenzoate 
• 17763-70-1 methyl 2-(trifluoromethylsulfonyloxy)benzoate 
• 530-78-9 flufenamic acid 

Downstream Products

• 114918-37-5 methyl 2-<(3-carbomethoxyphenyl)amino>benzoate 
• 42946-36-1 9-oxo-9,10-dihydro-acridine-2-carboxylic acid 
• 71507-02-3 9-oxo-9,10-dihydro-1-acridinecarboxylic acid 
• 106626-55-5 Acridine-1-carboxylic acid (2-dimethylamino-ethyl)-amide 

Relevant articles and documents

Photochemical transformation of flufenamic acid by artificial sunlight in aqueous solutions

In the present article, we have studied the photochemical behavior of a common non-steroidal anti-inflammatory drug (NSAIDs) namely flufenamic acid (FLUA) in aqueous solution. The absorption spectrum of such compound shows a significant absorption beyond

2,7-Dihydro-3H-pyridazino[5,4,3-kl]acridin-3-one derivatives, novel type of cytotoxic agents active on multidrug-resistant cell lines. Synthesis and biological evaluation

We have earlier postulated that the presence of a pyridazone ring fused with an anthracenedione moiety resulted in the analog's ability to overcome multidrug resistance of tumor cells [J. Med. Chem. 1999, 42, 3494]. High cytotoxic activity of obtained ant

Structure-activity relationship of quinazolinedione inhibitors of calcium-independent phosphodiesterase

A series of quinazolinediones and azaquinazolinediones is described which possess potent inhibitory activity toward the calcium-independent phosphodiesterase enzyme (CaIPDE). In vivo testing showed that this in vitro activity translates to animal models p