131613-53-1

Basic information

• Product Name: 2-(1-CARBOXY-ETHYL)-1,3-DIOXO-2,3-DIHYDRO-1H-ISOINDOLE-5-CARBOXYLIC ACID
• Synonyms: 2-(1-CARBOXY-ETHYL)-1,3-DIOXO-2,3-DIHYDRO-1H-ISOINDOLE-5-CARBOXYLIC ACID;AURORA 17310;OTAVA-BB BB7015511013
• CAS NO: 131613-53-1
• Molecular Formula: C12H9NO6
• Molecular Weight: 263.2
• Mol File: 131613-53-1.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(1-CARBOXY-ETHYL)-1,3-DIOXO-2,3-DIHYDRO-1H-ISOINDOLE-5-CARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(1-CARBOXY-ETHYL)-1,3-DIOXO-2,3-DIHYDRO-1H-ISOINDOLE-5-CARBOXYLIC ACID(131613-53-1)
• EPA Substance Registry System: 2-(1-CARBOXY-ETHYL)-1,3-DIOXO-2,3-DIHYDRO-1H-ISOINDOLE-5-CARBOXYLIC ACID(131613-53-1)

Safety Data

• Hazardous Substances Data: 131613-53-1(Hazardous Substances Data)

Usage

Molecular structure

2-(1-carboxy-ethyl)-1,3-dioxo-2,3-dihydro-1H-isoindole-5-carboxylic acid has a complex molecular structure, which includes a carboxylic acid derivative, a dioxo, and an isoindole functional group.

Functional groups

The compound contains a carboxylic acid derivative (-COOH), a dioxo group (cyclic structure with two oxygen atoms), and an isoindole ring (a benzene ring fused with a nitrogen-containing ring).

Pharmacological properties

Due to its unique structure, this chemical has the potential to exhibit various pharmacological properties, making it a candidate for further research in the field of medicinal chemistry.

Potential applications

The compound may have potential applications in the development of new drugs or therapies, but further research and analysis are needed to fully understand its potential uses and effects.

Research and analysis

To fully understand the potential uses and effects of 2-(1-carboxy-ethyl)-1,3-dioxo-2,3-dihydro-1H-isoindole-5-carboxylic acid, additional studies and experiments must be conducted to explore its pharmacological properties and potential applications in medicinal chemistry.

Upstream product

• 56-41-7 L-alanin 
• 552-30-7 trimellitic Anhydride 

Relevant articles and documents

The Special Modifiers Containing N-Trimellitylimido-L-Amino Acids for the Surface Modification of Nano ZrO2

The most important difficulties about nanoparticles (NPs) in liquid media involve stabilizing them. So, it is necessary to modify the NPs surface by modifiers to generate an effective repulsive force between them. Dispersion of NPs will influence their ap

Design of one-pot green protocol for the synthesis of novel modified LDHs with diacids based on amino acids: morphology and thermal examinations

In this study, a simple, fast and environmentally friendly protocol has been proposed for the synthesis of layered double hydroxides (LDHs) and organomodified chiral LDHs under ultrasound irradiation as a green and fast tool for the first time. Novel chiral LDHs were synthesized in one step from the co-precipitation reaction of the Al(NO3)3·9H2O, Mg(NO3)2·6H2O and different bioactive N-trimellitylimido-l-amino acids in aqueous state. The obtained materials were studied by several methods such as Fourier transformed infrared spectroscopy, X-ray diffraction, field emission scanning electron microscopy and transmission electron microscopy techniques. The results of structural and morphological analyses showed the successful intercalation of chiral diacids within the interlayer of LDH clay. Thermal properties were investigated by thermogravimetry analysis. The results showed that there were four weight loss steps during the thermal decomposition. The amino acid containing N-trimellitylimido diacid created a chiral environment in the modified LDH that could be used in the chiral field.

An effective and environmentally friendly method for surface modification of amorphous silica nanoparticles by biodegradable diacids derived from different amino acids

Commercially available silicon dioxide (SiO2) nanoparticles (NP)s were modified by chiral diacid coupling agents by ultrasonic irradiation. The acid groups can interact with the hydroxyl groups on the surface of SiO2 NPs. The interac