19279-70-0

Basic information

• Product Name: 2-[(4-methoxybenzylidene)amino]-1H-isoindole-1,3(2H)-dione
• CAS NO: 19279-70-0
• Molecular Formula: C₁₆H₁₂N₂O₃
• Molecular Weight: 280.2781
• Mol File: 19279-70-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 461.5°C at 760 mmHg
• Flash Point: 232.9°C
• Density: 1.27g/cm³
• Vapor Pressure: 1.07E-08mmHg at 25°C
• Refractive Index: 1.631
• CAS DataBase Reference: 2-[(4-methoxybenzylidene)amino]-1H-isoindole-1,3(2H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(4-methoxybenzylidene)amino]-1H-isoindole-1,3(2H)-dione(19279-70-0)
• EPA Substance Registry System: 2-[(4-methoxybenzylidene)amino]-1H-isoindole-1,3(2H)-dione(19279-70-0)

Safety Data

• Hazardous Substances Data: 19279-70-0(Hazardous Substances Data)

Usage

Organic compound

It is a carbon-based compound, as most of its structure is derived from carbon atoms and various functional groups.

Derivative of isoindole

The compound is derived from the heterocyclic compound isoindole, which is a fused bicyclic structure containing both carbon and nitrogen atoms.

Heterocyclic compound

The presence of nitrogen in its structure makes it a heterocyclic compound, which is a compound containing a ring of atoms with at least one non-carbon atom.

Benzylideneamino group

The compound contains a benzylideneamino group (-NH-C6H5), which is an aromatic amine group connected to a phenyl ring through a carbon atom.

Potential biological activities

The compound has been studied for its possible antimicrobial and anticancer properties, indicating its potential as a therapeutic agent.

Organic synthesis

2-[(4-methoxybenzylidene)amino]-1H-isoindole-1,3(2H)-dione has been explored for its potential use in organic synthesis, making it a versatile building block for creating new compounds.

Fluorescent probe

The compound has been researched as a potential fluorescent probe, which could be used to study biological processes or detect specific molecules in a sample.

Pharmaceutical and industrial applications

Due to its unique chemical structure and potential biological activities, the compound may have various applications in the pharmaceutical industry and other industrial settings.

Upstream product

• 1875-48-5 N-aminophthalamide 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 530740-41-1 2-[(4-methoxy-benzyl)-phenyl-amino]-isoindole-1,3-dione 
• 5705-18-0 1-(4-methoxybenzyl)-1-phenylhydrazine 
• 345928-21-4 2-((4-methoxybenzyl)amino)isoindoline-1,3-dione 

Relevant articles and documents

Extending the Scope of the B(C6F5)3-Catalyzed C=N Bond Reduction: Hydrogenation of Oxime Ethers and Hydrazones

The B(C6F5)3-catalyzed hydrogenation is applied to aldoxime triisopropylsilyl ethers and hydrazones bearing an easily removable phthaloyl protective group. The C=N reduction of aldehyde-derived substrates (oxime ethers and hydrazones) is enabled by using 1,4-dioxane as the solvent known to participate as the Lewis-basic component in FLP-type heterolytic dihydrogen splitting. More basic ketone-derived hydrazones act as Lewis bases themselves in the FLP-type dihydrogen activation and are therefore successfully hydrogenated in nondonating toluene. The difference in reactivity between aldehyde- and ketone-derived substrates is also reflected in the required catalyst loading and dihydrogen pressure.