65481-07-4

Basic information

• Product Name: 1H-Isoindole-1,3(2H)-dione, 2-[2-(2-propenyl)phenyl]-
• CAS NO: 65481-07-4
• Molecular Formula: C17H13NO2
• Molecular Weight: 263.296
• Mol File: 65481-07-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1H-Isoindole-1,3(2H)-dione, 2-[2-(2-propenyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Isoindole-1,3(2H)-dione, 2-[2-(2-propenyl)phenyl]-(65481-07-4)
• EPA Substance Registry System: 1H-Isoindole-1,3(2H)-dione, 2-[2-(2-propenyl)phenyl]-(65481-07-4)

Safety Data

• Hazardous Substances Data: 65481-07-4(Hazardous Substances Data)

Usage

Structure

A derivative of isoindole-1,3-dione with a phenyl group and a propenyl substituent

Usage

Commonly used in organic synthesis and medicinal chemistry

Potential applications

Drug development, chemical research, and material science

Reactivity

Unique structure and reactivity that may have potential pharmacological properties.

Upstream product

• 589-09-3 N-allyl-N-phenylamine 
• 85-44-9 phthalic anhydride 

Downstream Products

• 1351511-56-2 (E)-1-((4-methoxyphenyl)sulfonyl)-2-(prop-1-en-1-yl)indoline 
• 1351511-77-7 (E)-2-(2-(penta-2,4-dien-1-yl)phenyl)isoindoline-1,3-dione 
• 1351511-29-9 (E)-4-methoxy-N-(2-(penta-2,4-dien-1-yl)phenyl)benzenesulfonamide 
• 1351511-75-5 (E)-4-(2-(1,3-dioxoisoindolin-2-yl)phenyl)but-2-enal 

Relevant articles and documents

Regio- and enantioselective hydroamination of dienes by gold(I)/menthol cooperative catalysis

Alcohol is key: Regio- and enantioselective hydroamination of 1,3-dienes has been achieved with the dinuclear catalyst (R)-DTBM-SEGPHOS. The rate and selectivity of the reaction are enhanced by alcohol additives like menthol, which coordinates the cationic gold(I) to generate a Br?nsted acid that can participate in catalysis. Mbs=p-methoxybenzenesulfonyl. Copyright