103056-32-2

Basic information

• Product Name: 1H-Pyrrole-2,5-dione, 1-phenyl-3-(phenylthio)-
• CAS NO: 103056-32-2
• Molecular Formula: C16H11NO2S
• Molecular Weight: 281.335
• Mol File: 103056-32-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1H-Pyrrole-2,5-dione, 1-phenyl-3-(phenylthio)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole-2,5-dione, 1-phenyl-3-(phenylthio)-(103056-32-2)
• EPA Substance Registry System: 1H-Pyrrole-2,5-dione, 1-phenyl-3-(phenylthio)-(103056-32-2)

Safety Data

• Hazardous Substances Data: 103056-32-2(Hazardous Substances Data)

Upstream product

• 144328-37-0 2-chloro-N-phenyl-2-(phenylthio)succinimide 
• 84649-32-1 α-(phenylthio)maleic anhydride 
• 62-53-3 aniline 
• 941-69-5 N-phenyl-maleimide 
• 71724-33-9 1-phenyl-3-(phenylthio)pyrrolidine-2,5-dione 
• 108-98-5 thiophenol 
• 72000-67-0 3-bromo-1-phenyl-1H-pyrrole-2,5-dione 

Downstream Products

• 153615-79-3 2-(2,2'-biindol-3-yl)-N-phenylmaleimide 
• 174676-68-7 8a-Benzenesulfinyl-4-(tert-butyl-dimethyl-silanyloxy)-7-phenyl-5,5a,8a,8b-tetrahydro-furo[2,3-e]isoindole-6,8-dione 
• 174676-69-8 8a-(phenylsulfinyl)-4-methyl-7-phenyl-5,5a,8a,8b-tetrahydro-1-oxa-7-aza-as-indacene-6,8-dione 
• 153615-76-0 N-phenyl-2-(phenylsulphinyl)maleimide 

Relevant articles and documents

CARBON MONOXIDE RELEASING NORBORNENONE COMPOUNDS

The present invention provides organic compounds which are capable of releasing carbon monoxide under physiological conditions or pH trigger, and to the use of such compounds for conditioning a cell, tissue or organ, for example, to protect against ischaemic injury during a transplant event.

On the Cycloaddition Approach to Indolocarbazoles

2,2'-Biindolyl 9 reacts with electron-deficient dienophiles at 100-110 deg C to give low to moderate yields of Michael addition and formal cycloaddition products, with the former predominant; the products derived from 9 and 2-(phenylsulphinyl)maleimides 14 and 15 undergo in situ elimination of benzenesulphenic acid, leading to 2,2'-biindolyl-substituted maleimides which can be efficiently photocyclised into indolocarbazoles.