7702-03-6

Usage

Chemical Family

2-(4-carboxyphenyl)-1,3-dioxoisoindoline-5-carboxylic acid belongs to the family of isoindoline-1,3-diones.

Physical State

Crystalline, white solid.

Molecular Weight

311.25 g/mol.

Functional Groups

Contains two carboxylic acid functional groups and a phenyl group.

Synthesis

Often used in the synthesis of pharmaceuticals and organic compounds.

Medical Applications

Has potential applications in the field of medicine and drug development, specifically in the development of antibacterial and antiviral drugs.

Industrial Applications

Has potential uses in the synthesis of dyes and pigments due to its aromatic and acidic properties.

Upstream product

• 150-13-0 4-amino-benzoic acid 
• 552-30-7 trimellitic Anhydride 

Downstream Products

• 29747-29-3 2-(4-chlorocarbonyl-phenyl)-1,3-dioxo-1,3-dihydro-isoindole-5-carbonyl chloride 

Relevant academic research and scientific papers

Structure and reversible crystal-to-crystal transformations of a zinc(II) coordination polymer constructed from an imide-based dicarboxylic acid

An imide-based O-donor ligand, 4-carboxyphenyl-1,3-dioxoisoindoline-5-carboxylic acid (H2In-4-ba), and one Zn(II) coordination polymer, [Zn(In-4-ba)(py)2]n (1, py ?= ?pyridine), have been synthesized. Single-crystal X-ray

Synthesis and crystal structure of an expanded square grid metal organic material, [Cu(L1)(DMF)]n· (2.64 DMF)

A new square grid metal organic material, [Cu(L1)(DMF)]n· (2.64 DMF) (1; L1= N-(4-carboxyphenyl)-trimellitimide), has been prepared by solvothermal reaction of Cu(NO3)2·2.5H 2O, H2L1, and caffeine in

Synthesis and anti-inflammatory activity of sulfonamides and carboxylates incorporating trimellitimides: Dual cyclooxygenase/carbonic anhydrase inhibitory actions

Trimellitimides 6–21 were prepared and investigated in vivo for anti-inflammatory and ulcerogenic effects and in vitro for cytotoxicity. They were subjected to in vitro cyclooxygenase (COX-1/2) and carbonic anhydrase inhibition protocols. Compounds 6–11 a

Synthesis and characterization of new copoly(amide-imide)s and copoly amides with azo groups in their main chains

New aromatic copoly(amide-imide)s with high inherent viscosities were prepared by direct polycondensation reaction of diacides 2 or 5 and 4-nitro-1,2-phenylendiamine and three different derivatives of diacides 7 as a second diacides using triphenyl phosphite in N-methyl-2-pyrrolidone (NMP)/pyridine solution containing dissolved CaCl2. Their decomposition temperatures at 10% weight loss in nitrogen atmosphere were above 165 °C and the anaerobic char yield at 600 °C ranged from 46% to 74%. These polymers were readily soluble in various organic solvents and by their casting into transparent, tough and flexible films can be easily achieved.

METHODS OF MODULATING NEUROTROPHIN-MEDIATED ACTIVITY

Disclosed are compositions which modulate the interaction with nerve growth factor and precursors thereof with neurotrophic receptors. Also disclosed are methods of using the compositions of the invention, including methods of administration.

Reactive Imides as Curing Agents for Epoxy Resins. Part 1. Synthesis and Characterisation

A series of low molecular weight amine-terminated amide-imides (ATRs) has been prepared by reacting a dicarboxylic acid containing an imide group and diamines for use as curing agents for epoxy resins.The ATRs have been characterised by nitrogen analysis,

AROMATIC POLYESTERS CONTAINING HETEROCYCLIC UNITS

New aromatic polyesters have been synthesized by solution polycondensation of dihydroxyphenylquinoxalines with diacid chlorides containing preformed imide cycles. The thermal stability of these compounds is discussed and compared with related phenylquinox