7702-03-6

Basic information

• Product Name: 2-(4-carboxyphenyl)-1,3-dioxoisoindoline-5-carboxylic acid
• Synonyms: 2-(4-carboxyphenyl)-1,3-dioxoisoindoline-5-carboxylic acid;1H-isoindole-5-carboxylic acid, 2-(4-carboxyphenyl)-2,3-di;2-(4-carboxyphenyl)-1,3-diketo-isoindoline-5-carboxylic acid;2-(4-Carboxy-phenyl)-1,3-dioxo-2,3-dihydro-1H-isoindole-5-carboxylic acid;2-(4-carboxyphenyl)-1,3-dioxo-5-isoindolinecarboxylic acid;2-(4-carboxyphenyl)-1,3-dioxo-isoindole-5-carboxylic acid;2-(4-carboxyphenyl)-1,3-dioxoisoindole-5-carboxylic acid;BAS 00084698
• CAS NO: 7702-03-6
• Molecular Formula: C₁₆H₉NO₆
• Molecular Weight: 311.24576
• Mol File: 7702-03-6.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(4-carboxyphenyl)-1,3-dioxoisoindoline-5-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-carboxyphenyl)-1,3-dioxoisoindoline-5-carboxylic acid(7702-03-6)
• EPA Substance Registry System: 2-(4-carboxyphenyl)-1,3-dioxoisoindoline-5-carboxylic acid(7702-03-6)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 7702-03-6(Hazardous Substances Data)

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 articles and documents

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 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

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.