157103-14-5

Basic information

• Product Name: 7a-benzyl-4,5-dibromo-7-(4-methoxybenzyl)-3-methyloctahydrofuro[2,3,4-cd]isoindole-2,6-dione
• Synonyms: Furo(2,3,4-cd)isoindole-2,6-dione, octahydro-4,5-dibromo-7-((4-methoxyphenyl)methyl)-3-methyl-7a-(phenylmethyl)-
• CAS NO: 157103-14-5
• Molecular Formula: C₂₅H₂₅Br₂NO₄
• Molecular Weight: 563.2783
• Mol File: 157103-14-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 696.3°C at 760 mmHg
• Flash Point: 374.9°C
• Density: 1.58g/cm³
• Vapor Pressure: 3.1E-19mmHg at 25°C
• Refractive Index: 1.639
• CAS DataBase Reference: 7a-benzyl-4,5-dibromo-7-(4-methoxybenzyl)-3-methyloctahydrofuro[2,3,4-cd]isoindole-2,6-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 7a-benzyl-4,5-dibromo-7-(4-methoxybenzyl)-3-methyloctahydrofuro[2,3,4-cd]isoindole-2,6-dione(157103-14-5)
• EPA Substance Registry System: 7a-benzyl-4,5-dibromo-7-(4-methoxybenzyl)-3-methyloctahydrofuro[2,3,4-cd]isoindole-2,6-dione(157103-14-5)

Safety Data

• Hazardous Substances Data: 157103-14-5(Hazardous Substances Data)

Upstream product

• 157103-08-7 2-(4-methoxybenzyl)-2,3,3a,4,5,7a-hexahydro-5-methyl-1,3-dioxo-1H-isoindole-4-carboxylic acid 
• 2393-23-9 4-methoxy-benzylamine 
• 100-44-7 benzyl chloride 
• 157103-13-4 3-benzyl-2,3,3a,4,5,7a-hexahydro-3-hydroxy-2-(4-methoxybenzyl)-5-methyl-1-oxo-1H-isoindole-4-carboxylic acid lactone 

Relevant articles and documents

Synthesis and biological activity of a series of isoindolone derivatives related to cytochalasins

A series of hydrogenated isoindolone derivatives structurally related to cytochalasin B has been synthesized and their ability to induce binucleation in the human lymphocytes were tested. All compounds were found able to inhibit cell cytokinesis at different extent in the range (3.12-25 μmol/l) respect to the negative control; however the highest percentage of binucleated cells is induced by Cyt B.