114875-64-8

Usage

Molecular structure

The compound has both isoindole and pyridine structures, with a 1,4-dihydro-4-oxo-2-pyridinyl group attached to a diphenylmethoxy moiety, which is linked to the isoindole core.

Molecular weight

The molecular weight of the compound is 431.45 g/mol.

Potential applications

1H-Isoindole-1,3(2H)-dione, 2-[[1,5-bis(diphenylmethoxy)-1,4-dihydro-4-oxo-2-pyridinyl]methoxy]may have potential pharmacological or industrial applications.

Further research needed

The compound would need to be further studied and characterized to determine its specific properties and potential uses.

Upstream product

• 524-38-9 N-hydroxyphthalimide 
• 908093-98-1 diazodiphenylmethane 
• 114875-62-6 5-(benzhydryloxy)-1-hydroxy-2-(hydroxymethyl)pyridin-4(1H)-one 
• 59281-02-6 5-benzhydryloxy-2-(hydroxymethyl)-pyran-4-one 
• 501-30-4 5-hydroxy-2-(hydroxymethyl)-4H-pyran-4-one 

Relevant academic research and scientific papers

Synthesis and in vitro antibacterial activity of new aminothiazole-oximepiperidone cephalosporins

Four new aminothiazole-oximepiperidone cephalosporins (10a-10d) were synthesized, with their in vitro antibacterial activities against hospital isolated Gram-negative bacteria assessed. The results showed that compounds 10a-10d effectively inhibit a varie

C-3 tetrahydrofuran substituted cephalosporin-siderophore conjugate as well as preparation method and application thereof

The invention discloses a C-3-tetrahydrofuran substituted cephalosporin-siderophore conjugate as well as a preparation method and application of the C-3-tetrahydrofuran substituted cephalosporin-siderophore conjugate. The invention discloses the C-3 tetra

3-(Heteroaryl acetamido)-2-oxo-azetidine-1-sulfonic acids derivatives as antibacterial agents

The present invention relates to novel Syn isomers of racemates and optical isomers of 3-(heteroaryl acetamido)-2-oxo-azetidine-1-sulfonic acids of formula (I) and its use in treating the infections caused by gram-negative pathogenic bacteria.

Cephalosporin compounds, and antibacterial agents

A cephalosporin compound having the formula: STR1 wherein R1 is a hydrogen atom, a halogen atom, a methoxy group, a substituted or unsubstituted vinyl group, or --CH2 --A wherein A is a hydrogen atom, an azido group, an acyloxy group